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Food and human safety: the impact of microplastics

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Abstract

Plastic waste pollution is one of the biggest problems in the world today. The amount of plastic in the environment continues to increase, and human exposure to microplastic (MP) has become a reality. This subject has attracted the attention of the whole world. The MP problem has also been noticed by the scientific community. The term microplastic is mostly used to define synthetic material with a high polymer content that can have a size range from 0.1 to 5000 µm. This paper aims to characterize the routes of exposure to MP, define its pollution sources, and identify food types contaminated with plastics. This review addresses the current state of knowledge on this type of particles, with particular emphasis on their influence on human health. Adverse effects of MP depend on routes and sources of exposure. The most common route of exposure is believed to be the gastrointestinal tract. Sources of MP include fish, shellfish, water as well as tea, beer, wine, energy drinks, soft drinks, milk, salt, sugar, honey, poultry meat, fruits, and vegetables. Studies have shown that particles of PET, PE, PP, PS, PVC, PA, and PC are the most frequently found in food.

Introduction

Plastics are materials composed of polymers and additives such as fillers, plasticizers, pigments, stabilizers, flame retardants, anti-static, and foaming agents that improve physical and processing properties. In the beginning of 1950s, the production of plastic products has steadily increased (Novotna et al. Citation2019). In 2021, the plastics and rubber products’ market were worth approx. $1,229.98 billion. This market is expected to grow to $1357.49 billion in 2022 (+10.4%) and to $1923.6 billion in 2026 (+9.1% of each year) (“Plastics and rubber products global market report 2022” Citation2022).

Plastics can be found in all branches of life and economy. Goods made of this material show many positive features, such as lightness and durability – resistance to mechanical damage, corrosion, and weather conditions (Bott, Störmer, and Franz Citation2014). Unfortunately, the popularity of such products has also its negative consequences. One of the biggest problems of the modern world is plastic waste, the amount of which increased significantly during the COVID-19 pandemic (Shi Citation2021). In the EU, 80–85% of marine litter is plastics, of which 50% are single-use products (Yuan, Nag, and Cummins Citation2022).

Nearly 40% of global plastic production is used by packaging (Hirt and Body-Malapel Citation2020; Shlush and Davidovich-Pinhas Citation2022). Therefore, it is one of the main sources of microplastic (MP) (Koelmans et al. Citation2022; Lozano et al. Citation2021).

Microplastic is a synthetic material with a high polymer content (Jadhav et al. Citation2021). It characterizes with a size range from 0.1 to 5000 µm (). However, due to technical limitations, detection at sizes smaller than 1 μm does not yet have adequate technical support. Therefore, the minimum size for MP recognition is currently considered to be 1 µm. Depending on the size, these materials are usually divided into small and large MPs. 50% of MPs in aquatic systems are between 500 and 1000 µm, 29.8% are between 1000 and 2500 µm, while 17.6% are between 2500 and 5000 µm. Large MPs in the marine environment decompose into smaller particles by mechanical action, photooxidation, and hydrolytic degradation (Batool et al. Citation2022; Liu, Xu, et al. Citation2022). The toxicity of MPs is related to their size, the smaller the size, the greater the predicted toxicity (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Figure 1. Sizes of plastics.

Figure 1. Sizes of plastics.

This contaminant is ubiquitous in the environment, the air we breathe and in the food we eat. Various types of plastics can be found in food. The largest amounts of MP are made from the following polymers: poly(ethylene terephthalate) – PET (Oßmann et al. Citation2018; Schymanski et al. Citation2018), polyethylene – PE (Çobanoğlu et al. Citation2021; Wang et al. Citation2022), polypropylene – PP (Hwang et al. Citation2019), polystyrene – PS (Huang et al. Citation2022; Liu, Hou, et al. Citation2022), poly(vinyl chloride) – PVC (Qin et al. Citation2022), polyamide – PA (Deshoulles et al. Citation2022), and polycarbonate – PC (Shi et al. Citation2021) ().

Table 1. The properties of microplastic present in food.

Microplastic is a health problem, raising ecological, and food safety concerns (Lee and Fang Citation2022). It attracts the attention of the whole world: authorities, public opinion, media, as well as ecological and non-governmental organizations (Yuan, Nag, and Cummins Citation2022). This problem has also been noticed by the scientific community (Sridhar et al. Citation2022). The number of papers dealing with MP has increased more than 100-fold over the last ten years (). There is also a growing awareness of the problem and number of questions that the scientific community is trying to answer. A key question with respect to MP is to what extent and in what way does it cause risk to human health? This article will attempt to answer this question. This paper aims to characterize the routes of exposure to MP, define its pollution sources, and identify food types contaminated with this material.

Figure 2. The number of articles concerning microplastic from 2012 to 2021 (based on source: ScienceDirect).

Figure 2. The number of articles concerning microplastic from 2012 to 2021 (based on source: ScienceDirect).

Methods

The analysis of the current state of knowledge was based on studies on MPs published in international databases: ScienceDirect, PubMed, and Scopus. The databases were filtered by search terms in title, abstract, and keywords with the following expressions: microplastic and food. The most relevant literature sources were included in this review. Priority was given to articles published during the last three years. Over 190 studies on microplastic were reviewed.

Classification

Until recently, MP analysis has focused on aquatic environments, primarily the living organisms. However, these contaminants are also considered an emerging threat to terrestrial ecosystems. Many food products of different origins can be contaminated with MP. The derivation, size, shape as well as polymer type (), and concentration are key properties when studying the effects of these types of particles on the aquatic and terrestrial environment (Lozano et al. Citation2021).

Primary and secondary microplastics

Microplastics can be classified according to their origin, and there can be distinguished primary and secondary types (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Primary MPs are particles of manufactured products, such as personal hygiene. They can be residues of toothpaste, hair gel, cleansing lotion, and particulate air fresheners. They usually enter the environment with discharged domestic wastewater (Anagnosti et al. Citation2021; Hwang et al. Citation2020; Xu et al. Citation2022). Investigations of MP presence in toothpaste resulted in findings of PP, PVC, and PA particles within 100 and 399 μm. Irregularly shaped microparticles – fragmentary – were the most abundant and accounted for 63–98% of all MPs, followed by fibrous particles in an amount of 2–35% (Madhumitha et al. Citation2022).

Secondary MPs are the unintentional debris of plastic degradation. They are obtained from “meso (5–25 mm)” and “macro (>25 mm)” plastic waste by physical, chemical, and biological processes (Olewnik-Kruszkowska et al. Citation2020; Olewnik-Kruszkowska, Nowaczyk, and Kadac Citation2016, Citation2017). Plastic waste undergoes several processes but the photodegradation was found to be the most common route of MPs formation (Periyasamy and Tehrani-Bagha Citation2022; Xi et al. Citation2022). Their main sources besides plastic waste fragments (e.g. packaging) are paints removed from various types of plastic products and fibers from fishing equipment and textiles (Muthu Citation2021).

Shape

Microplastics can be found in different forms. Their categorization is enabled by the size and color sorting system (SCS), which is used to characterize these particles according to their appearance (Crawford and Quinn Citation2017). There are ten shape categories in the SCS system (). Some authors suggest further categorization of MPs shapes as spheres, cylindrical, disc-shaped, flat, egg-shaped, elongated, and rounded particles (Toussaint et al. Citation2019). Their shapes are influenced by the following factors: initial form of the material, time strictly affecting the degradation processes of a material and the conditions/environment in which the material is located (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Table 2. The categorization of MP based on shape.

Color

The SCS assumes that each MP particle must be assigned a color (Crawford and Quinn Citation2017) but combinations of colors are allowed ().

Color is an important factor affecting aquatic organisms. Microplastics found in surface seawater samples and in sediments are usually colorless or white, while multicolored and black ones are less common. Due to the similarity in color, animals may mistake their natural food for MP and ingest it, for example, fish often eat white and transparent plastic fibers. This is the way, MP can enter the food chain and be ingested by humans (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Table 3. The categorization of MP based on color.

Routes of exposure to microplastics

The effects of MPs on the human body depend on the routes of exposure. Exposure can occur through the inhalation, the skin contacts and the mucous membrane covering the eye surfaces, or the ingestion of contaminated food (Celebi Sö et al. Citation2020; Hwang et al. Citation2020; Yang, Man, et al. Citation2022).

The inhalation

Airborne MPs can be found around the world (Ebrahimi et al. Citation2022). Their concentration is known to increase in areas with high population and human activity, especially indoors. Working conditions are also important in the context of respiratory exposure to them. Microplastic deposition and accumulation were confirmed in human lung tissue. The largest number of particles was discovered in the lower part of the lung versus the upper and mid parts. There were identified 12 polymer types in 11 of 13 human lung tissue samples, with the most abundant PP (23%) and PET (18%) (Jenner et al. Citation2022). It was found that MP may cause respiratory diseases (Jenner et al. Citation2022; Kumar et al. Citation2022; Prata Citation2018). It caused airway and interstitial inflammatory reactions as well as dyspnea (Prata Citation2018).

The contact by the skin and the mucous membrane of eye

Dermal absorption of MPs may occur through the use of personal care products, and even direct contact with them (e.g. PS) can damage the skin (Hwang et al. Citation2020).

The mucous membrane covering the eye surfaces is also exposed to MPs from hygiene products. After 48 h of exposure to polystyrene particles on the eye surface of mice resulted in oxidative stress, decreased cell viability, and apoptosis. After 4 weeks, MPs’ (2 µm) deposition was found in the conjunctival sac, and the number of goblet cells in the conjunctival sac of the lower eyelid decreased up to 40% compared to the cells in the control group. In addition, so-called dry eye, ocular surface damage, and conjunctivitis and lacrimal glands were observed (Zhou et al. Citation2022).

The ingestion of contaminated food

The most common route of exposure to MPs is believed to be through the gastrointestinal tract. They can be ingested involuntarily. It was estimated that people worldwide may consume 0.1–5 g of these particles per week (Senathirajah et al. Citation2021). After oral exposure to MP, dangerous substances (e.g. polycyclic aromatic hydrocarbon – PAH and polychlorinated biphenyl – PCB) can appear in the gastrointestinal tract (Kumar et al. Citation2022).

Some MP is excreted from the human body with feces (Luqman et al. Citation2021; Schwabl et al. Citation2019; Zhang et al. Citation2021). Poly(ethylene terephthalate) was the most often identified in these samples. Fecal examinations confirmed that the concentration of PET in infant feces was 10 times higher than in adult samples. Particularly disturbing is the information that MP was also detected in meconium samples (Zhang et al. Citation2021). As MP was discovered in human feces, it is believed that it can directly affect the microbiota (Lu et al. Citation2019).

Sources of microplastic

Microplastics constitute the serious problem of global concern. These particles are omnipresent in aquatic and terrestrial environments. Their sources can be everyday objects and contaminated food.

Environment

Considering the problem of MP food contamination is not possible without referring to environmental pollution. Their accumulation has been confirmed in deep seas and oceans, surface and groundwater, soils, coastal sediments, Arctic snow and Antarctic ice, and beaches. Studies on MPs spreading point to wastewater treatment plants as a common source from which they can enter natural waters, groundwater, or terrestrial ecosystems (Zurier and Goddard Citation2021).

Water reservoirs

The vast majority of marine pollution comes from land, that is, 4.8–12.7 million tons of plastic per year (Haward Citation2018). It has been found that over 250 000 tons of MP may be floating in the oceans. However, plastic particles concentrations tend to decrease gradually with distance from industrial sources. Their higher amounts are found in urbanized regions with high population density (Talbot and Chang Citation2022). It is likely that MPs ingested by humans originate from these locations (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Soil

Microplastics are also found in soil environments (Ren et al. Citation2022; Tian et al. Citation2022; Zhang, Kim, et al. Citation2022). They may affect soil biota including microorganisms (e.g. Proteobacteria). Plastic particles impact the soil bacterial phylogenetic profile (Fajardo et al. Citation2022). It was found that MP can be transferred from soil to plants and then from plant food to humans (Shi Citation2021).

Insects

Microplastics can be also carried by organisms, for example, honey bees. The presence of MP attached to the body of bees has been reported. Thirteen synthetic polymers were detected, of which polyesters were the most common, followed by PE and PVC (Edo et al. Citation2021). Exposure to PS reduced the diversity of bee gut microflora, changed gene expression, was associated with oxidative damage, and detoxification (al Naggar et al. Citation2021). Microplastic was found in 12% of the honey samples tested (Diaz-Basantes, Conesa, and Fullana Citation2020; Al Naggar et al. Citation2021). It was concluded that synthetic particles can be brought into the hive by bees during nectar collection (Liebezeit and Liebezeit Citation2015; Nowak and Nowak Citation2021).

Households

Microplastics are ubiquitous not only in environments, but also in households. Nowadays, fabrics, household appliances, disposable or reusable food containers, bottles, jars, cups, caps, and other packaging made of plastic are used intensively. Such objects are usually made of PET, PP, PVC, PS, high-density polyethylene (HDPE), and low-density polyethylene (LDPE) (Geueke, Groh, and Muncke Citation2018; Hahladakis et al. Citation2018; Hahladakis and Iacovidou Citation2018; Lozano et al. Citation2021).

Packaging

The popularity of plastic packaging has led researchers to analyze their effects on human health in terms of MP release from various types of food containers (Jadhav et al. Citation2021). Takeaway containers made from popular polymer materials (PP, PS, PE, and PET) were subjected to investigation (Du, Cai, et al. Citation2020). Microplastics originated from all the analyzed products, and their quantity ranged from 3 to 29 pieces/container. The highest density was found in PS containers with rough surfaces which easily chipped under the influence of low mechanical force. Therefore, the production of PS-based packaging for food and beverage has been restricted by a decision of the European Parliament in 2021 (Du, Cai, et al. Citation2020).

Microplastic can enter children’s bodies through pacifiers, toys, contaminated food, and by crawling on carpets and floors made of plastic. One of the primary sources of MP for children is plastic bottles. The release of these contaminants from baby bottles was analyzed (Li et al. Citation2020). These containers were pre-cleaned and sterilized. After drying under natural conditions, water at 70 °C was poured into the bottles. The average number of MPs per liter of water amounted to 4 million while the maximum was 16.2 million (Li et al. Citation2020).

Food preparation, cooking, and processing

Microplastics can be introduced into food chain during food preparation, cooking, and processing. It has been estimated that 100–300 MPs/mm are formed on a plastic cutting board during food preparation (Luo et al. Citation2022). Plastic particles can be also released from the surface of food containers when exposed to microwave or oven heating (Marazuela et al. Citation2022). The effect of heat treatment of disposable plastic materials on the release of MPs in an aqueous environment was investigated. It was found that soaking in water at approximately 100 °C released 1.07, 1.44, 2.24, and 1.57 million particles/ml from plastic packaging, cups, transparent boxes, and expandable boxes, respectively (Liu, Wang, et al. Citation2022).

Food with microplastic

Microplastics constitute a potential threat to human health due to their widespread presence in foods we eat. The most common plastic particles found in food are blue-colored and fiber-shaped (Bai et al. Citation2022).

Sources of MPs for humans can be beverages and foods such as water (Koelmans et al. Citation2019; Kosuth, Mason, and Wattenberg Citation2018; Schymanski et al. Citation2018; Shruti, Pérez-Guevara, and Kutralam-Muniasamy Citation2020; Vega-Herrera et al. Citation2022; Wiesheu et al. Citation2016), tea (Afrin, Rahman, Akbor, et al. Citation2022; Shruti, Pérez-Guevara, Elizalde-Martínez, et al. Citation2020), beer (Diaz-Basantes, Conesa, and Fullana Citation2020; Kosuth, Mason, and Wattenberg Citation2018; Lachenmeieret al. Citation2015; Liebezeit and Liebezeit Citation2014; Shruti, Pérez-Guevara, Elizalde-Martínez, et al. Citation2020; Shruti et al. Citation2021), wine (Prata et al. Citation2020), energy drinks (Shruti, Pérez-Guevara, Elizalde-Martínez, et al. Citation2020), soft drinks (Shruti, Pérez-Guevara, Elizalde-Martínez, et al. Citation2020), animal products, including fish (Karami, Golieskardi, Bin Ho, et al. Citation2017; Karami et al. Citation2018; Karthik et al. Citation2018; O’Connor et al. Citation2022; Pan et al. Citation2022; Peters et al. Citation2018), shellfish (Chinfak et al. Citation2021; Daniel et al. Citation2021; Ding et al. Citation2020; Fernández Severini et al. Citation2020; Li et al. Citation2015; Pan et al. Citation2022), salt (Gündoğdu Citation2018; Iñiguez, Conesa, and Fullana Citation2017; Karami, Golieskardi, Choo, et al. Citation2017; Kosuth, Mason, and Wattenberg Citation2018; Manimozhi et al. Citation2022; Yang et al. Citation2015), sugar (Afrin, Rahman, Hossain, et al. Citation2022; Liebezeit and Liebezeit Citation2013) and honey (Liebezeit and Liebezeit Citation2013), milk (Kutralam-Muniasamy et al. Citation2020), poultry meat (Kedzierski et al. Citation2020), plants, including fruits, and vegetables (Oliveri Conti et al. Citation2020) (). This chapter will present, in the authors’ opinion, the most interesting examples of foods in which MP is found.

Table 4. Microplastic in food.

Beverages

The largest amount of research that links MP and food topics relates to beverages, in particular water. Microplastics were detected in both bottled (Oßmann et al. Citation2018; Schymanski et al. Citation2018) and tap water (Novotna et al. Citation2019). Plastic microparticles were present in water in the form of fragments and fibers.

Mineral water in PET bottles constitutes an example of the increase of human exposure to MPs. It was found that disposable PET bottles were characterized with MPs concentrations ranging from 0.1 to 1.8 μg/dm3, while for reusable bottles these values increased several times up to 0.6–7.3 μg/dm3 (Oßmann et al. Citation2018; Schymanski et al. Citation2018). Therefore, significant amounts of plastic particles were released by food and beverage containers as a result of peeling of their inner surface during washing (both with hot water − 95 °C, and with cold water – with ice added). These treatments were reported to result in the formation of MPs in an average amount of 176 particles/dm3 (Hee, Weston, and Suratman Citation2022).

Microplastic was also confirmed in water from households (Vega-Herrera et al. Citation2022) and public places (Shruti, Pérez-Guevara, and Kutralam-Muniasamy Citation2020). Tap water samples from around the world were tested and 81% of them were contaminated. The average concentration was 5.45 particles/dm3 (Kosuth, Mason, and Wattenberg Citation2018). In the case of tap water from China, the lowest measured MP count was 440 particles/l. Most of the particles were PE and PP, which were smaller than 50 μm (Tong et al. Citation2020). The household tap water of the Barcelona Metropolitan Area was also contaminated with PE and PP. These particles had a size of 7–20 μm (Vega-Herrera et al. Citation2022). In addition, the presence of MP has been confirmed in free public drinking water fountains. Microplastics were detected in all the drinking water samples (42), with an average amounting to 18 MP/dm3. Transparent (69%), blue (24%), and red (7%) fibers, mainly made of PET and epoxy resin, were identified. Most particles had dimensions between 0.1 and 1 mm (Shruti, Pérez-Guevara, and Kutralam-Muniasamy Citation2020).

The researches on MP content in water are particularly important because it is the basis for many beverages, for example, tea, energy drinks, soft drinks and alcohol. Contaminated water negatively affects their quality, but product packaging is also important. Plastic particles were found to leach from the tea bags. Using electron microscopy, it was stated that a single brewed tea bag releases about 11.6 billion MPs into the water (Hernandez et al. Citation2019). The same effect was observed after the consumption of hot drinks, such as tea and coffee, from disposable cups (Ranjan, Joseph, and Goel Citation2021).

Microplastics are present in alcohol, for example, in beer or wine. There are many reports of MP in beer (Diaz-Basantes, Conesa, and Fullana Citation2020; Lachenmeieret al. Citation2015; Liebezeit and Liebezeit Citation2014; Shruti, Pérez-Guevara, Elizalde-Martínez, et al. Citation2020; Shruti et al. Citation2021; Wiesheu et al. Citation2016) but only one article about the presence of plastic in wine (Prata et al. Citation2020). In the first case, PE and PET were the most popular, while in the second case PE was the most common. In both cases, these particles were usually fiber-shaped (Diaz-Basantes, Conesa, and Fullana Citation2020; Kosuth, Mason, and Wattenberg Citation2018; Lachenmeier et al. Citation2015; Liebezeit and Liebezeit Citation2014; Shruti, Pérez-Guevara, Elizalde-Martínez, et al. Citation2020; Shruti et al. Citation2021).

There are also reports of MP being present in other popular beverages, such as energy drinks and soft drinks. Plastic, in the form of fibers, was found in almost 80% of the samples tested, for example, PA, poly(acrylonitrile-butadiene-styrene) – ABS, poly(ester amide) – PEA (Shruti, Pérez-Guevara, Elizalde-Martínez, et al. Citation2020). These particles originated from textiles and packaging.

Based on the collected data it can be concluded that PE, in the form of fibers, is the most common beverage contaminant.

Fish and shellfish

Microplastics are ubiquitous pollutants of aquatic ecosystems and are reported to interact with a wide range of aquatic organisms. Fish and shellfish constitute the popular food matrix in which MP can be found (Gao et al. Citation2022; Gündogdu et al. Citation2022; O’Connor et al. Citation2022).

In Ireland, it is estimated that 73% of deep-sea fish ingest plastic (Eriksen et al. Citation2014). Fragments of PET are the most commonly found in fish. This situation is a particular problem for commercially important species due to the reduction in yields and resulting in economic losses. Fish accumulate plastic particles in their gut (Bouwmeester, Hollman, and Peters Citation2015), which is not generally consumed. Therefore, MP found in fish gut cannot be considered a direct threat to human health (Pan et al. Citation2022). However, plastic particles are able to enter the food chain at higher trophic levels as inedible parts of fish can be used as animal feed ingredients (Bouwmeester, Hollman, and Peters Citation2015).

A different situation is observed for shellfish. Polyethylene and poly(ethylene terephthalate) microparticles in the form of fibers were the most popular plastic contaminants in these animals (Chinfak et al. Citation2021; Daniel et al. Citation2021; Li et al. Citation2015; Pan et al. Citation2022). Microplastic was found in bivalves, squids and shrimps, which are filter feeders (Daniel et al. Citation2021; Li et al. Citation2015). Bivalve mollusks directly transfer MP to higher trophic levels, because their digestive tract is usually eaten (Farrell and Nelson Citation2013; Fernández Severini et al. Citation2020).

Fish and shellfish are consumed globally. However, there are animal species that are consumed regionally, that is, the sea cucumber (Apostichopus japonicus). It is commercially fished or farmed and subsequently consumed in Asian cuisines. The presence of plastic particles in the edible parts of sea cucumber has been confirmed. Microplastic quantity decreased when the analyzed organisms were transferred to clean water. However, trace amounts of MP in their bodies were found for many days after transfer (Mohsen et al. Citation2022).

Spices

Spices, in particular salt and sugar, can also be a popular source of MP for human. The occurrence of MPs in salt products of various types, for example, commercial brands of table salt, rock salt, and laboratory NaCl was investigated. MP content ranged from 11 to 193, 64, and 253 pcs/kg, respectively. PE in fiber form in such products was most common (Kapukotuwa et al. Citation2022).

Moreover, sugar from both Europe and Asia were contaminated mostly with MP fibers. However, particles separated from samples from Germany were smaller than the ones from Bangladesh, that is, > 40 μm (Liebezeit and Liebezeit Citation2013) and <300 μm, respectively (Afrin, Rahman, Hossain, et al. Citation2022). Poly(acrylonitrile-butadiene-styrene) and poly(vinyl chloride) were most common in European sugar (Liebezeit and Liebezeit Citation2013). Plastic particles in Asian honey were not identified structurally (Afrin, Rahman, Hossain, et al. Citation2022).

Food from terrestrial animals

The common group of foods are products derived from terrestrial animals. These can be products made by animals (e.g. honey and milk) as well as animal tissues or organs.

The occurrence of MP in honey and milk was confirmed. In the first case, the plastic particles were of environmental origin, and in the second case, of technological origin. Plastic fibers of a size greater than 40 µm, most likely carried by bees with pollen, were found in honey. This pollution was at a level of 166 MPs/kg (Liebezeit and Liebezeit Citation2013). In contrast, milk contained particles, mainly polyethersulfone (PES) and polysulfone (PSU) in the form fibers, up to 500 µm. Microplastic contamination of milk resulted from the technological processing, because PES and PSU are commonly used as membrane materials in dairy processes (Kutralam-Muniasamy et al. Citation2020).

In addition, MP particles can be found in poultry meat. Packaged meat was contaminated in the range from 4.0 to 18.7 MP/kg. Particles were in the form of fibers and were difficult to remove by rinsing. These were PS particles that most likely originated from the packaging (Kedzierski et al. Citation2020).

In summary, MP contamination in foods of animal origin was the result of the environment contamination as well as technological processing. Microplastic transmission within the animal body was not considered as a possible cause of contamination. This topic is important because MP can transmit to organs (Lu et al. Citation2018). Unfortunately, the presence of MP in offal has not yet been described.

Plants

Microplastic can penetrate the seeds, roots, culms, leaves and fruits (Dietz and Herth Citation2011). It can affect the plant growth, development and functioning, including the germination, inhibit roots and leaves growth, the tissue composition (Fajardo et al. Citation2022). Microplastic impact differs depending on plant species and polymer types (Rillig et al. Citation2019), and its uptake is inversely proportional to the size (Bosker et al. Citation2019).

The effect of particles’ shape on plant biomass was investigated. Microplastic in fiber forms increased plant biomass because these particles hold water in the soil. Foams and fragments increased soil aeration and macroporosity, while films decreased soil bulk density (Lozano et al. Citation2021). Microplastic was able to transfer from plant roots to leaves (Shi Citation2021). It was found that particles can penetrate rice roots and move to aboveground parts. Plastic accumulation was confirmed in the vascular systems of plant tissues, especially in vascular bundles and leaf veins, and in cell walls and intercellular areas (Liu, Guo, et al. Citation2022). In addition, MP contamination of agroecosystems reduces food yields (Tian et al. Citation2022), for example, as a result of PS exposure a reduction in pea (Pisum sativum) yield of more than 30% was observed (Kim et al. Citation2022).

Microplastic was also detected in fruits and vegetables of edible plants with apples (Malus domestica) and carrots (Daucus carota) as the most polluted. The lettuce (Lactuca sativa) was the least polluted. The plastic particles in fruits and vegetables had 1.56–3.19 µm and 1.36–2.95 µm in size, respectively (Oliveri Conti et al. Citation2020). It can be concluded that fruits are characterized with a higher MP contamination compared to vegetables. It might be due to the submitted root system, the big vascularization of the pulp, and the tree age (Oliveri Conti et al. Citation2020). In another research, the accumulation of PE in broccoli and radish sprouts was confirmed. Radish was more affected by MP contamination than broccoli (López et al. Citation2022).

The effect of polymethylmethacrylate (PMMA) on rapeseed (Brassia campestris L.) was also evaluated, and inhibition of germination rate was observed (Dong et al. Citation2022). Based on the confirmed MP effects on rapeseed, it is reasonable to investigate the plastic particles content in cooking oil. Attention should be paid to the widespread consumption of rapeseed oil. Unfortunately, such researches are not currently available.

Other

According to Amiri et al. (Citation2022) the route of exposure to MP may be through the gastrointestinal tract, but the source need not be food. Increased exposure to plastic particles has been observed in individuals suffering from geophagy, an eating disorder that involves intentional soil consumption or similar materials. Soil from Hormoz Island (Iran) was found to contain PET, PA, PS, and PP fibers. This is particularly disturbing as it is used to prepare traditional spices, extremely popular in this region, the use of which is both culinary and cultural (Amiri et al. Citation2022).

Health impacts

Microplastic can exhibit different types and degrees of toxicity (Lithner, Larsson, and Dave Citation2011), which depends on the properties of the polymers (and individual mers), the sizes of particles, and shapes (Santana, Moreira, and Turra Citation2017). Current scientific evidence confirmed that MP concentration, exposure time, the presence of additives used during plastic processing, modification of the particle surface and hydrophobicity are also important (Guerrera et al. Citation2021).

Poly(vinyl chloride), polystyrene, polyacrylonitrile (PAN), poly(acrylonitrile-co-butadiene-co-styrene) (ABS), and epoxy resin are classified as the most toxic polymers based on monomer toxicity (Yuan, Nag, and Cummins Citation2022). Greater histological abnormalities have been found in freshwater mussels due to exposure to PVC and PS, compared to PET and PE (Rochman et al. Citation2017). Monomers, such as vinyl chloride, styrene and chemicals derived from phenolic compounds, for example, alkylphenols, brominated flame retardants, and bisphenol A, are known toxicants. The presence of these substances should be one of the main purposes of MP toxicity evaluation (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Microplastic can cause acute and chronic toxicity. The toxic effects of MP include: developmental, reproductive and locomotor toxicity, neurotoxicity, immunotoxicity, genotoxicity, and cytotoxicity (Bhagat et al. Citation2020). The increase in antioxidant defense after exposure to MP indicates that oxidative stress is induced (Du, Xu, et al. Citation2020; Tagorti and Kaya Citation2022).

The health effects of MPs depend on their location in the body () (Kwon et al. Citation2020; Yang, Man, et al. Citation2022). Microplastics have been found inside organisms, on skin and in hair, saliva, and fecal samples (Ebrahimi et al. Citation2022). Plastic particles can affect human health both indirectly and directly (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Table 5. Health effects of microplastic.

Indirect health impacts

Indirect health impacts of MP is due to the fact that their surfaces provide an ideal environment for pathogens to grow, thus, making them carriers of biological contaminants. In addition, plastics can transport chemical pollutants.

Pathogens on MP surface

Pathogens that can form specific layers on the surface of MP are fungi, bacteria, and protozoa. Microplastics create a favorable environment for microorganisms as they bind water and nutrients. The pathogens can cause, for example, dysbiosis, which reduces host immunity and promotes infections (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Pathogenic fungi accumulate on the surface of MPs, grow and multiply but also become resistant to temperature and sunlight (Gkoutselis et al. Citation2021). The surface of plastic particles can be covered with slimy layers of sediment or biofilm that allow pathogens to adhere, mutate and exchange DNA (the collection of exogenous DNA) (Mehrabi et al. Citation2011). Microplastics can also serve as carriers for antibiotic-resistant bacteria. Some bacterial strains living in biofilms increase antibiotic resistance by up to 30-fold (Pham, Clark, and Li Citation2021).

The adhesion of pathogens to the MP surface mainly depends on the type and shape of the particles. Microsized PE spheres and polyester fibers were found to be carriers for protozoa Toxoplasma gondii, Cryptosporidium parvum, and Giardia enterica which cause parasitic diseases in humans and animals. Interestingly, larger numbers of parasites adhere to the surface of microfibers than to microspheres (Zhang, Kim, et al. Citation2022).

Microplastic as a carrier of chemical pollutants

Microplastic affects the absorption and release of chemical contaminants as well as the transport of substances such as additives (e.g. tetrabromobisphenol A – TBBPA), heavy metals (e.g. Mn, Zn, As, Cr, Cu, Pb, and Ni), organic pollutants (e.g. PCB), medicines (e.g. methylene blue), and pesticides (e.g. carbendazim – KAR, dipterex – DIP, diflubenzuron – DIF, malathion – MAL, difenoconazole – DIFE, imidacloprid – IMD, buprofezin – BPF, and difenoconazole – DFZ). It can exacerbate the harmful effects of contaminants (Chen et al. Citation2017; Rainieri et al. Citation2018; Rainieri and Barranco Citation2019; Rochman et al. Citation2013).

Heavy metals

Once released into the aquatic environment, the MP surface can be colonized by biofilm which can also increase the adsorption of contaminants. Polystyrene particles of approximately 75 μm and 4000 μm, on which a biofilm of freshwater fungus Acremonium strictums had formed, were investigated. The biofilm increased heavy metal adsorption on MP and particle size played a key role in this process as well as biofilm colonization. It was found that particles of about 75 μm can carry more biofilm on their surface than those with a size of 4000 μm. There are more functional groups on the surface of the former MPs compared to the latter, which promotes electrostatic interactions and chemical association of heavy metals. The 75 μm particles show a greater capacity for Cu adsorption and Cr(VI) reduction, which may be associated with functional groups in the biofilm (Wu et al. Citation2022).

Microplastics act as carriers of heavy metals. Metal ions are adsorbed on the surface or adjacent layers, mainly through electrostatic interactions and complexation (Kinigopoulou et al. Citation2022). Adsorbed metals can diffuse into the solutions in which they are present. Significant release of Mn, Zn, As, Cr, Cu, and Ni from the MP surface in NaCl solution and Mn, Zn, As, Cr, Cu, Pb, and Ni in gastrointestinal solutions was found (Chen et al. Citation2022).

There was also analyzed the transfer of Cu and Pb from MP (polyamide 12 – PA12 and polylactide – PLA) into catfish organisms Clarias gariepinus, which are a major food source in Southeast Asia. Fish were reared for three months and exposed to seven different feed combinations supplemented with plastics and metals. At monthly intervals, fish gills, intestines, liver and edible muscle were analyzed for Cu and Pb. It was found that PLA carried higher amounts of metals compared to PA12. The highest metal concentrations were observed in gills, followed by liver, intestines, and edible muscles of fish (Jang et al. Citation2022).

Pesticides

The affinity and release of harmful substances vary depending on the type and concentration of both plastic and other contaminants as well as the degradation of MPs surface. Due to their small size, large specific surface area, and hydrophobicity, plastic particles are ideal carriers of hydrophobic substances such as pesticides, for example, KAR, DIP, DIF, MAL, DIFE. These substances are adsorbed in the following order DIF > DIFE > MAL > KAR > DIP. It was found that MPs can increase the harmfulness of pesticides through their adsorption and desorption. The adsorption kinetics and isotherm studies indicate that surface interactions as well as mass transfer and intramolecular diffusion are involved in the adsorption process. Therefore, the contaminants’ adsorption process is determined by both physical factors and chemical interactions. In contrast, thermodynamic studies show that pesticides’ adsorption is a spontaneous and exothermic process (Li et al. Citation2021; Wang, Gao, et al. Citation2022).

The presence of polyethylene MP can significantly prolong the half-lives of pesticides in water, for example, the half-life of terbuthylazine increases from 31.8 days to 45.2 days in the presence of 10 μg/dm3 MP (Wang, Gao, et al. Citation2022). High pH, low salinity, and elevated temperature promote the adsorption of pesticides such as IMD, BPF, DFZ. The adsorption capacity of the mentioned substances on PE was as follows: DFZ > BPF > IMD, (Li et al. Citation2021).

Other chemicals

Microplastic also enhances TBBPA accumulation in a commercial mussel species (Tegillarca granosa). It is dangerous because TBBPA is considered an endocrine disruptor and an immunotoxic agent (Zhang, Kim, et al. Citation2022). Similar observations were made in studies performed on zebra fish and sea bass (Granby et al. Citation2018). Higher concentrations of PCB and brominated flame retardants – BFR were detected in the muscle tissue of fish fed pellets containing a combination of contaminants and MP compared to those with feed containing only contaminants without plastic particles (Granby et al. Citation2018).

In addition, the impact of PS at 3 mg/dm3, phenanthrene (PHE) 0.2 mg/dm3 and a combination of both parameters was tested on zebra fish. The interaction of MP and PHE boosted oxidative damage, stimulated immune response, and changed microbial composition (Xu et al. Citation2021).

Microplastics released into the environment are degraded by mechanical abrasion and exposure to ultraviolet radiation. In a study by Hüffer, Weniger, and Hofmann (Citation2018), HDPE and PP were subjected to accelerated aging under atmospheric conditions using ultraviolet irradiation with or without hydrogen peroxide. The adsorption of two model contaminants, PHE, and methylene blue, was evaluated. Physical and chemical characterization of the particles showed that aging led to significant surface oxidation and micro-crack formation (Hüffer, Weniger, and Hofmann Citation2018). The affinity of PHE and methylene blue for MP was stronger in this case compared to the degraded materials versus the undegraded materials. Microplastic oxidation can increase the adsorption of organic pollutants (Bhagat et al. Citation2022).

It can be concluded that MP increased the uptake of harmful compounds by organisms. The adsorption of organic contaminants is higher on particles subjected to accelerated degradation processes than on original ones. It was found that PE adsorbs more organic compounds (e.g. PCBs) than other plastics (e.g. PP and PVC) (Teuten et al. Citation2009). Among the most common mechanisms of sorption of organic contaminants on MP can be listed as hydrophobic interaction, followed by electrostatic interactions (e.g. Van Der Waalsa), hydrogen bonding, halogen bonding, and π–π interactions (Li et al. Citation2021). Therefore, the increase of the potential food safety hazards can be observed (Kwon et al. Citation2020; Yang, Man, et al. Citation2022).

Direct health impacts

Direct health impacts of MP concern the exposure to MP related to the type of polymer, size, and shape of the particles and the presence of additives used at the plastic processing stage. When analyzing the effects of plastics on human health, monomers such as vinyl chloride and styrene deserve particular attention. Some authors suggest that the presence of these substances should be one of the main targets of research evaluating the influence of MP on human health (Sánchez et al. Citation2022). Besides polymers, MPs also contain chemicals, intentionally added during the production of plastics, which can cross the intestinal barrier (Sánchez et al. Citation2022). The presence of additives used in plastics processing is often overlooked. This approach is inappropriate as the processing of poly(vinyl chloride) requires plasticizers, including phthalates, or phthalic esters, which can constitute up to 50% of the mass. They affect the hormone balance, increase the risk of allergies, and cause infertility problems (Rana et al. Citation2020). Microplastic can affect not only the body but also the psyche of the test organisms.

Aquatic animals

The consumption of MP may have adverse effects on aquatic organisms (Dimitriadi et al. Citation2021; Jin et al. Citation2018; de Marco et al. Citation2022; Qiao et al. Citation2019b; Tang et al. Citation2018; Tarasco et al. Citation2022; Zhao et al. Citation2021). Different species of fish (e.g. zebrafish) are often used in in vivo studies of, for example, intestinal diseases (Dimitriadi et al. Citation2021; Jin et al. Citation2018; de Marco et al. Citation2022; Qiao et al. Citation2019a; Tang et al. Citation2018; Tarasco et al. Citation2022; Zhao et al. Citation2021).

When taken orally, MPs can end up in the stomach. The predominant polymer (65%) found in the stomach of the flathead grey mullet is PE (Avio, Gorbi, and Regoli Citation2015). Microplastics can be absorbed through the gastrointestinal tract and transported to other parts of the body in different species of fish, both saltwater and freshwater (Guerrera et al. Citation2021). They can cross the intestinal barrier and reach organs such as the liver in commercial fish species Mugil cephalus (Avio, Gorbi, and Regoli Citation2015). Microplastic with a diameter of 5 μm accumulates in the fish gills, liver, and intestines, whereas the one with a diameter of 20 μm only in the gills and intestines. Microplastic can also affect physiological processes (Li, Chen et al. Citation2022). It can induce local inflammation in tissues and organs of animals (Hwang et al. Citation2020), lipid accumulation in the liver (Ebrahimi et al. Citation2022; Lu et al. Citation2016; Yin et al. Citation2021), intestinal dysbiosis, inflammatory bowel disease and the changes of the intestinal microflora in zebrafish (Souza-Silva et al. Citation2022). High intake of plastics may reduce the absorption of ingested food, thus, leading to reduced energy intake, which may have further consequences for the growth, or development of organisms (Ruthsatz et al. Citation2022), and fertility, such as in copepods (Lee et al. Citation2013). The rate of MP excretion is also important (Santana, Moreira, and Turra Citation2017) because contaminants can be metabolized by organisms and, thus, adversely affect their functioning (Gray Citation2002).

Polystyrene particles significantly increase superoxide dismutase and catalase activities in zebrafish. Metabolomic analysis suggests that MP induces changes in metabolic profiles in fish liver and disrupts lipid and energy metabolism (Lu et al. Citation2016). Similar studies on zebrafish exposure to polystyrene MP were performed using 5 μm microspheres (50 μg/dm3 and 500 μg/dm3). After 21 days of testing, there were observed changes in enzyme biomarkers and significant histological shifts associated with inflammation and oxidative stress. Significant changes in the gut microbiome and gut metabolic profiles in zebrafish were also identified. The study by Qiao et al. (Citation2019a) provided evidence that exposure to MP can cause intestinal damage (Qiao et al. Citation2019a). In another study by Jin et al. (Citation2018), male zebrafish was exposed to PS of 0.5 and 50 µm for 14 days (100 and 1000 μg/dm3). As a result, gut mucus volume increased, microflora dysbiosis and inflammation in the gut of adult zebrafish were observed. In addition, 0.5 µm MPs caused an increase in IL1α, IL1β and IFN mRNA and protein levels in the gut (Jin et al. Citation2018).

Furthermore, in addition to the digestive system, the immune system is also exposed to significant MP effects. The immune system recognizes the enemy in plastic particles, reacts violently at first, and then weakens (Santana, Moreira, and Turra Citation2017). Acute exposure to MP resulted in immune system impairment, such as in the scleractinian coral Pocillopora damicornis. A significant decrease in alkaline phosphatase enzyme was observed (Tang et al. Citation2018).

Terrestrial animals

Terrestrial mammals constitute a popular model organism used during analyses of the health effects of MP (Deng et al. Citation2022; Hwang et al. Citation2019; Kwon et al. Citation2022; Li, Chen,, et al. Citation2022; Liu, Zhuan, et al. Citation2022; Liu, Hou, et al. Citation2022; Meng et al. Citation2022; Mu et al. Citation2022; Sun, Chen, et al. Citation2021; Sun, Xu, et al. Citation2021; Tomazic-Jezic, Merritt, and Umbreit Citation2001; Wang, Zhao, et al. Citation2021; Zaheer et al. Citation2022).

Polystyrene particles with diameters of 0.46 and 1 µm affected red blood cells (RBCs) and caused hemolysis. Red blood cells of sheep were used in this study, because their structure and function are similar to human (Hwang et al. Citation2020). Microplastic with sizes from 0.1 µm to 10 µm was found in rabbits’ lymph, from 30 to 40 µm in rodents’ lymph (Yuan, Nag, and Cummins Citation2022), whereas PVC microparticles of 5–100 µm in the portal vein of dogs (Volkheimer Citation1975).

Microplastics can cross the blood-brain barrier and it was observed in a study conducted on mice. Researchers orally administered plastic particles up to 2 µm in diameter to mice for 7 days. It was found that MPs accumulated in microglia cells accompanying neurons and deteriorated their ability to multiply. This resulted in apoptosis, changes in immune response and inflammatory reactions (Kwon et al. Citation2022). As a mouse is a common mammal model, the findings presented and the health risks of MP to animals should not be ignored.

The health effects of MPs are related to their size. Particles smaller than 20 μm can penetrate organs in mammalian bodies (Lusher, Hollman, and Mendoza-Hill Citation2017). Polystyrene accumulation was observed in the kidney and liver of mice. Male mice orally exposed to 1000 μg PS/dm3 for 5 weeks were characterized by decreased body and liver weights, as well as the number of lipids (Lu et al. Citation2018). In addition, there was observed a phagocytosis in mouse macrophages as a result of exposure to 1.4 µm and 6.4 µm polymethylmethacrylate (PMMA) and 1.2, 5.2, and 12.5 µm PS particles (Tomazic-Jezic, Merritt, and Umbreit Citation2001). Particles below 150 μm in size can induce systemic exposure, be absorbed by living organisms, migrate through the intestinal wall, and reach lymph nodes (Lusher, Hollman, and Mendoza-Hill Citation2017). Particles larger than 150 μm are not absorbed but can cause local inflammatory effects (Presence of Microplastics and Nanoplastics in Food, with Particular Focus on Seafood Citation2016; Yuan, Nag, and Cummins Citation2022).

Currently, it is thought that environmental factors may be one of the causes of autism spectrum disorder (ASD) development (Gaugler et al. Citation2014). It is the group of etiologically distinct conditions that led to similar behavioral manifestations. Prenatal and postnatal exposures to PE lead to ASD-like traits in a mouse model (e.g. problems in social interactions). In addition, this contact resulted in gut microbiome amendments, the alteration of glucose metabolism, and the increase of the expression of EGR-1 and AGR genes. This is particularly important because ASD patients have gastrointestinal disorders. Moreover, mutations in EGR-1 have been linked to ASD (Zaheer et al. Citation2022). However, further research is needed to establish a link between the presence of MP in the body and autism.

Humans

There are few studies in the literature on the effects of MP on humans (Bonanomi et al. Citation2022; Çobanoğlu et al. Citation2021; Gautam et al. Citation2022; Hwang et al. Citation2019, Citation2020; Ju et al. Citation2020; Kwon et al. Citation2022; Lee et al. Citation2021; Wang, Zhao, et al. Citation2021; Wu et al. Citation2019; Zhang, Kim, et al. Citation2022). Most analyses have been conducted on human cells, such as peripheral blood mononuclear cells (Çobanoğlu et al. Citation2021; Hwang et al. Citation2019), umbilical vein endothelial cells HUVEC (Lee et al. Citation2021), HaCaT keratinocyte cells (Gautam et al. Citation2022), dermal fibroblasts (Hwang et al. Citation2020), lung epithelial A549 cells (Hwang et al. Citation2020), microglial HMC-3 cells (Kwon et al. Citation2022), kidney proximal tubular epithelial cells HK-2 (Wang, Zhao, et al. Citation2021), cells of intestinal epithelial Caco-2 (Gautam et al. Citation2022; Wu et al. Citation2019), small intestinal epithelial cells HIEC-6 (Zhang, Kim, et al. Citation2022), colonic epithelial cell CCD841CoN (Zhang, Kim, et al. Citation2022) and intestinal CCD-18Co cells (Bonanomi et al. Citation2022). Cells exposed to MP experience cell death three times faster than when exposed to other foreign bodies. The rate of their regeneration also decreases significantly as a result of this contact (Nienke Vrisekoop van UMC Utrecht onderzoekt gevaren van microplastics Citation2019). Zhang, Kim, et al. (Citation2022) found that MP damages cell membranes ( Zhang, Kim, et al. Citation2022). The particles with sizes of 0.–5 µm were more likely to induce cell apoptosis after short-term exposure, compared to MPs with sizes less than 0.2 µm (Banerjee et al. Citation2022).

The presence of MP in human body fluids has been also confirmed. Some of blood samples contained up to three types of plastics, approximately 50% of the samples contained PET, approx. 30% – PS, and approx. 25% – PE. It is particularly important as it shows that MPs are present in the bloodstream and can penetrate organs via this route (Leslie et al. Citation2022).

In the body, MP releases toxic substances (e.g. TBBPA, styrene, vinyl chloride) that can cause various diseases, including cancer (Bonanomi et al. Citation2022). Polysytrene in the form of MP induces an immune response and stimulates the production of cytokines and chemokines. Interleukin-6 (IL-6) secretion also increases after contact with PS particles (diameter ˂3 µm, concentration = 500 µg/cm3) (Hwang et al. Citation2020). Long-term exposure of HepG2 liver cells to functionalized PS resulted in increased levels of interleukin-8 (IL-8), a key pro-inflammatory cytokine (Banerjee et al. Citation2022).

Nanoplastic

Plastic particles can acquire toxic properties with decreasing size (Stock et al. Citation2022). Particles smaller than MP with a size between 1 and 100 nm are called nanoplastic (NP), which is characterized by a high toxicity. This is caused by its very small particle sizes and large specific surface area. In the intestine, NP causes stronger inflammation and oxidative stress than MP. Nanoplastic can enter tissues, whereas MP is often blocked and cannot fully exert its toxic effects (Lusher, Hollman, and Mendoza-Hill Citation2017).

The studies showed that the harmfulness of plastic depended on particle size, surface functionalization, exposure time and dose. It was found that 50 nm PS induced apaptosis to SNU-1 human gastric epithelial cells. A higher apoptosis rate was observed with aminated particles compared to carboxylated or non-functionalized particles (Banerjee, Billey, and Shelver Citation2021).

In addition, NP destroys the cell membrane integrity of gametes and causes toxic effects on progeny as it is transferred across the placenta in a mice. Administration of PS during gestation produced a negative impact on fetuses and led to anxiety-like behaviors of progenies. Additionally, these particles caused apoptosis in neuronal cell lines, oxidative damage, and inhibited γ-aminobutyric acid synthesis in a brain (Yang, Zhu, et al. Citation2022).

It can be concluded that NP induces higher toxicity including reproductive and neurotoxicity than MP (Yin et al. Citation2021). Thus, the monitoring of the level and harmfulness of these particles is particularly important.

Conclusions

Microplastic is a ubiquitous contaminant that can be found in air, water, and soil. The most common route of exposure to MP is believed to be through the gastrointestinal tract. It poses a significant threat to human health due to its widespread occurrence in food. In addition, MP carries pollutants and microbial pathogens into living organisms. It can be accumulated in the body, induce inflammation, and have adverse effects on the immune, endocrine, reproductive and digestive systems. Exposure to MP is associated with a risk of oxidative stress, changes in cell division and viability, DNA damage, immune responses, metabolic disruption, intestinal dysbiosis, increased risk of cancer, respiratory, and neurodegenerative diseases. Microplastic can affect both the body and the psyche of the test organisms. It is supposed that plastic particles may be one of the causes of ASD.

Unfortunately, gaps in analytical methodologies make a comprehensive understanding of MP problem difficult. The standardization of requirements and the implementation of uniform experimental procedures for plastic particles are essential to ensure proper food quality. It will allow the real assessment of health risks associated with the presence of MP in food products.

Disclosure statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Funding

The author(s) reported there is no funding associated with the work featured in this article.

References

  • Afrin, S., M. Rahman, A. Akbor, A. B. Siddique, K. Uddin, and G. Malafaia. 2022. Is there tea complemented with the appealing flavor of microplastics? A pioneering study on plastic pollution in commercially available tea bags in Bangladesh. The Science of the Total Environment 837:155833. doi: 10.1016/j.scitotenv.2022.155833.
  • Afrin, S., M. Rahman, N. Hossain, K. Uddin, and G. Malafaia. 2022. Are there plastic particles in my sugar? A pioneering study on the characterization of microplastics in commercial sugars and risk assessment. Science of The Total Environment 837:155849. doi: 10.1016/j.scitotenv.2022.155849.
  • Al Naggar, Y., M. Brinkmann, C. M. Sayes, S. N. Al-Kahtani, S. A. Dar, H. R. El-Seedi, B. Grünewald, and J. P. Giesy. 2021. Are honey bees at risk from microplastics? Toxics 9 (5):109. doi: 10.3390/toxics9050109.
  • Amiri, H., M. Hoseini, S. Abbasi, M. Malakootian, M. Hashemi, N. Jaafarzadeh, and A. Turner. 2022. Geophagy and microplastic ingestion. Journal of Food Composition and Analysis 106:104290. doi: 10.1016/j.jfca.2021.104290.
  • Anagnosti, L., A. Varvaresou, P. Pavlou, E. Protopapa, and V. Carayanni. 2021. Worldwide actions against plastic pollution from microbeads and microplastics in cosmetics focusing on european policies. Has the issue been handled effectively? Marine Pollution Bulletin 162:111883. doi: 10.1016/j.marpolbul.2020.111883.
  • Avio, C. G., S. Gorbi, and F. Regoli. 2015. Experimental development of a new protocol for extraction and characterization of microplastics in fish tissues: First observations in commercial species from Adriatic Sea. Marine Environmental Research 111:18–26. doi: 10.1016/j.marenvres.2015.06.014.
  • Bai, C.-L., L.-Y. Liu, Y.-B. Hu, E. Y. Zeng, and Y. Guo. 2022. Microplastics: A review of analytical methods, occurrence and characteristics in food, and potential toxicities to biota. The Science of the Total Environment 806 (Pt 1):150263. doi: 10.1016/j.scitotenv.2021.150263.
  • Banerjee, A., L. O. Billey, A. M. McGarvey, and W. L. Shelver. 2022. Effects of polystyrene micro/nanoplastics on liver cells based on particle size, surface functionalization, concentration and exposure period. The Science of the Total Environment 836:155621. doi: 10.1016/j.scitotenv.2022.155621.
  • Banerjee, A., L. O. Billey, and W. L. Shelver. 2021. Uptake and toxicity of polystyrene micro/nanoplastics in gastric cells: Effects of particle size and surface functionalization. Plos One 16 (12):e0260803. doi: 10.1371/journal.pone.0260803.
  • Batool, I., A. Qadir, J. M. Levermore, and F. J. Kelly. 2022. Dynamics of airborne microplastics, appraisal and distributional behaviour in atmosphere; a review. The Science of the Total Environment 806 (Pt 4):150745. doi: 10.1016/j.scitotenv.2021.150745.
  • Bhagat, K., A. C. Barrios, K. Rajwade, A. Kumar, J. Oswald, O. Apul, and F. Perreault. 2022. Aging of microplastics increases their adsorption affinity towards organic contaminants. Chemosphere 298:134238. doi: 10.1016/j.chemosphere.2022.134238.
  • Bhagat, J., L. Zang, N. Nishimura, and Y. Shimada. 2020. Zebrafish: An emerging model to study microplastic and nanoplastic toxicity. The Science of the Total Environment 728:138707. doi: 10.1016/j.scitotenv.2020.138707.
  • Bonanomi, M., N. Salmistraro, D. Porro, A. Pinsino, A. M. Colangelo, and D. Gaglio. 2022. Polystyrene micro and nano-particles induce metabolic rewiring in normal human colon cells: A risk factor for human health. Chemosphere 303 (Pt 1):134947. doi: 10.1016/j.chemosphere.2022.134947.
  • Bosker, T., L. J. Bouwman, N. R. Brun, P. Behrens, and M. G. Vijver. 2019. Microplastics accumulate on pores in seed capsule and delay germination and root growth of the terrestrial vascular plant lepidium sativum. Chemosphere 226:774–81. doi: 10.1016/j.chemosphere.2019.03.163.
  • Bott, J., Á. Störmer, and R. Franz. 2014. A model study into the migration potential of nanoparticles from plastics nanocomposites for food contact. Food Packaging and Shelf Life 2 (2):73–80. doi: 10.1016/j.fpsl.2014.08.001.
  • Bouwmeester, H., P. C. H. Hollman, and R. J. B. Peters. 2015. Potential health impact of environmentally released micro- and nanoplastics in the human food production chain: Experiences from nanotoxicology. Environmental Science & Technology 49 (15):8932–47. doi: 10.1021/acs.est.5b01090.
  • Celebi Sö, Z., L. Cevhertas, K. Nadeau, M. Akdis, and C. A. Akdis. 2020. Environmental factors in epithelial barrier dysfunction. The Journal of Allergy and Clinical Immunology 145 (6):1517–28. doi: 10.1016/j.jaci.2020.04.024.
  • Chen, G., Q. Fu, X. Tan, H. Yang, Y. Luo, M. Shen, and Y. Gu. 2022. Speciation and release risk of heavy metals bonded on simulated naturally-aged microplastics prepared from artificially broken macroplastics. Environmental Pollution (Barking, Essex : 1987) 295:118695. doi: 10.1016/j.envpol.2021.118695.
  • Chen, Q., D. Yin, Y. Jia, S. Schiwy, J. Legradi, S. Yang, and H. Hollert. 2017. Enhanced uptake of BPA in the presence of nanoplastics can lead to neurotoxic effects in adult zebrafish. The Science of the Total Environment 609:1312–21. doi: 10.1016/j.scitotenv.2017.07.144.
  • Chinfak, N., P. Sompongchaiyakul, C. Charoenpong, H. Shi, T. Yeemin, and J. Zhang. 2021. Abundance, composition, and fate of microplastics in water, sediment, and shellfish in the Tapi-Phumduang River system and Bandon Bay, Thailand. Science of The Total Environment 781:146700. doi: 10.1016/j.scitotenv.2021.146700.
  • Çobanoğlu, H., M. Belivermiş, E. Sıkdokur, Ö. Kılıç, and A. Çayır. 2021. Genotoxic and cytotoxic effects of polyethylene microplastics on human peripheral blood lymphocytes. Chemosphere 272:129805. doi: 10.1016/j.chemosphere.2021.129805.
  • Crawford, C. B, and Quinn, B. 2017. Microplastic Pollutants. Amsterdam, Netherlands: Elsevier.
  • de Souza-Silva., T. G. I. A. Oliveira, G. G. d Silva, F. C. V. Giusti, R. D. Novaes, and H. A. d Almeida Paula. 2022. Impact of microplastics on the intestinal microbiota: A systematic review of preclinical evidence. Life Sciences 294:120366. doi: 10.1016/j.lfs.2022.120366.
  • Daniel, D. B., P. M. Ashraf, S. N. Thomas, and K. T. Thomson. 2021. Microplastics in the edible tissues of shellfishes sold for human consumption. Chemosphere 264:128554. doi: 10.1016/j.chemosphere.2020.128554.
  • de Marco, G., G. Oliveri Conti, A. Giannetto, T. Cappello, M. Galati, C. Iaria, E. Pulvirenti, F. Capparucci, A. Mauceri, M. Ferrante, et al. 2022. Embryotoxicity of polystyrene microplastics in zebrafish Danio rerio. Environmental Research 208:112552. doi: 10.1016/j.envres.2021.112552.
  • Deng, J., M. S. Ibrahim, L. Y. Tan, X. Y. Yeo, Y. A. Lee, S. J. Park, T. Wüstefeld, J. W. Park, S. Jung, and N. J. Cho. 2022. Microplastics released from food containers can suppress lysosomal activity in mouse macrophages. Journal of Hazardous Materials 435:128980. doi: 10.1016/j.jhazmat.2022.128980.
  • Deshoulles, Q., M. le Gall, C. Dreanno, M. Arhant, D. Priour, and P. Y. le Gac. 2022. Chemical coupling between oxidation and hydrolysis in polyamide 6 - a key aspect in the understanding of microplastic formation. Polymer Degradation and Stability 197:109851. doi: 10.1016/j.polymdegradstab.2022.109851.
  • Diaz-Basantes, M. F., J. A. Conesa, and A. Fullana. 2020. Microplastics in honey, beer, milk and refreshments in ecuador as emerging contaminants. Sustainability 12 (14):5514. doi: 10.3390/su12145514.
  • Dietz, K. J, and S. Herth. 2011. Plant nanotoxicology. Trends in Plant Science 16 (11):582–9. doi: 10.1016/j.tplants.2011.08.003.
  • Dimitriadi, A., C. Papaefthimiou, E. Genizegkini, I. Sampsonidis, S. Kalogiannis, K. Feidantsis, D. C. Bobori, G. Kastrinaki, G. Koumoundouros, D. A. Lambropoulou, et al. 2021. Adverse effects polystyrene microplastics exert on zebrafish heart – Molecular to individual level. Journal of Hazardous Materials 416:125969. doi: 10.1016/j.jhazmat.2021.125969.
  • Ding, J., J. Li, C. Sun, F. Jiang, C. He, M. Zhang, P. Ju, and N. X. Ding. 2020. An examination of the occurrence and potential risks of microplastics across various shellfish. Science of The Total Environment 739:139887. doi: 10.1016/j.scitotenv.2020.139887.
  • Dong, R., R. Liu, Y. Xu, W. Liu, L. Wang, X. Liang, Q. Huang, and Y. Sun. 2022. Single and joint toxicity of polymethyl methacrylate microplastics and As (V) on rapeseed (Brassia Campestris L.). Chemosphere 291:133066. doi: 10.1016/j.chemosphere.2021.133066.
  • Du, F., H. Cai, Q. Zhang, Q. Chen, and H. Shi. 2020. Microplastics in take-out food containers. Journal of Hazardous Materials 399:122969. doi: 10.1016/j.jhazmat.2020.122969.
  • Du, J., S. Xu, Q. Zhou, H. Li, L. Fu, J. Tang, Y. Wang, X. Peng, Y. Xu, and X. Du. 2020. A review of microplastics in the aquatic environmental: Distribution, transport, ecotoxicology, and toxicological mechanisms. Environmental Science and Pollution Research International 27 (11):11494–505. doi: 10.1007/s11356-020-08104-9.
  • Ebrahimi, P., S. Abbasi, R. Pashaei, A. Bogusz, and P. Oleszczuk. 2022. Investigating impact of physicochemical properties of microplastics on human health: A short bibliometric analysis and review. Chemosphere 289:133146. doi: 10.1016/j.chemosphere.2021.133146.
  • Edo, C., A. R. Fernández-Alba, F. Vejsnaes, J. J. M. van der Steen, F. Fernández-Piñas, and R. Rosal. 2021. Honeybees as active samplers for microplastics. The Science of the Total Environment 767:144481. doi: 10.1016/j.scitotenv.2020.144481.
  • Eriksen, M., L. C. M. Lebreton, H. S. Carson, M. Thiel, C. J. Moore, J. C. Borerro, F. Galgani, P. G. Ryan, and J. Reisser. 2014. Plastic pollution in the world’s oceans: More than 5 trillion plastic pieces weighing over 250,000 tons afloat at sea. PLoS One. 9 (12):e111913. doi: 10.1371/journal.pone.0111913.
  • Fajardo, C., C. Martín, G. Costa, S. Sánchez-Fortún, C. Rodríguez, J. J. de Lucas Burneo, M. Nande, G. Mengs, and M. Martín. 2022. Assessing the role of polyethylene microplastics as a vector for organic pollutants in soil: Ecotoxicological and molecular approaches. Chemosphere 288 (Pt 1):132460. doi: 10.1016/j.chemosphere.2021.132460.
  • Farrell, P, and K. Nelson. 2013. Trophic level transfer of microplastic: Mytilus edulis (L.) to Carcinus Maenas (L.). Environmental Pollution (Barking, Essex : 1987) 177:1–3. doi: 10.1016/j.envpol.2013.01.046.
  • Fernández Severini, M. D., N. S. Buzzi, A. D. Forero López, C. V. Colombo, G. L. Chatelain Sartor, G. N. Rimondino, and D. M. Truchet. 2020. Chemical composition and abundance of microplastics in the muscle of commercial shrimp Pleoticus muelleri at an impacted coastal environment (Southwestern Atlantic). Marine Pollution Bulletin 161:111700. doi: 10.1016/j.marpolbul.2020.111700.
  • Gao, P., N. Q. I. M. Noor, and S. M. Shaarani. 2022. Current status of food safety hazards and health risks connected with aquatic food products from Southeast Asian region. Critical Reviews in Food Science and Nutrition 62 (13):3471–89. doi: 10.1080/10408398.2020.1866490.
  • Gaugler, T., L. Klei, S. J. Sanders, C. A. Bodea, A. P. Goldberg, A. B. Lee, M. Mahajan, D. Manaa, Y. Pawitan, J. Reichert, et al. 2014. Most genetic risk for autism resides with common variation. Nature Genetics 46 (8):881–5. doi: 10.1038/ng.3039.
  • Gautam, R., J-h Jo, M. Acharya, A. Maharjan, D-e Lee, P. Bahadur, C-y Kim, K. Kim, H-a Kim, and Y. Heo. 2022. Evaluation of potential toxicity of polyethylene microplastics on human derived cell lines. The Science of the Total Environment 838 (Pt 2):156089. doi: 10.1016/j.scitotenv.2022.156089.
  • Geueke, B., K. Groh, and J. Muncke. 2018. Food packaging in the circular economy: Overview of chemical safety aspects for commonly used materials. Journal of Cleaner Production 193:491–505. doi: 10.1016/j.jclepro.2018.05.005.
  • Gkoutselis, G., S. Rohrbach, J. Harjes, M. Obst, A. Brachmann, M. A. Horn, and G. Rambold. 2021. Microplastics accumulate fungal pathogens in terrestrial ecosystems. Scientific Reports 11 (1):13214. doi: 10.1038/s41598-021-92405-7.
  • Granby, K., S. Rainieri, R. R. Rasmussen, M. J. J. Kotterman, J. J. Sloth, T. L. Cederberg, A. Barranco, A. Marques, and B. K. Larsen. 2018. The influence of microplastics and halogenated contaminants in feed on toxicokinetics and gene expression in European seabass (Dicentrarchus labrax). Environmental Research 164:430–43. doi: 10.1016/j.envres.2018.02.035.
  • Gray, J. S. 2002. Biomagnification in marine systems: The perspective of an ecologist. Marine Pollution Bulletin 45 (1-12):46–52. doi: 10.1016/S0025-326X(01)00323-X.
  • Guerrera, M. C., M. Aragona, C. Porcino, F. Fazio, R. Laurà, M. Levanti, G. Montalbano, G. Germanà, F. Abbate, and A. Germanà. 2021. Micro and nano plastics distribution in fish as model organisms: Histopathology, blood response and bioaccumulation in different organs. Applied Sciences 11 (13):5768. doi: 10.3390/app11135768.
  • Gündoğdu, S. 2018. Contamination of table salts from Turkey with microplastics. Food Additives & Contaminants. Part A, Chemistry, Analysis, Control, Exposure & Risk Assessment 35 (5):1006–14. doi: 10.1080/19440049.2018.1447694.
  • Gündogdu, S., N. Rathod, A. Hassoun, E. Jamroz, P. Kulawik, C. Gokbulut, A. Aït-Kaddour, and F. Özogul. 2022. The impact of nano/micro-plastics toxicity on seafood quality and human health: Facts and gaps. Critical Reviews in Food Science and Nutrition :1–19. doi: 10.1080/10408398.2022.2033684.
  • Hahladakis, J. N, and E. Iacovidou. 2018. Closing the loop on plastic packaging materials: What is quality and how does it affect their circularity? The Science of the Total Environment 630:1394–400. doi: 10.1016/j.scitotenv.2018.02.330.
  • Hahladakis, J. N., C. A. Velis, R. Weber, E. Iacovidou, and P. Purnell. 2018. An overview of chemical additives present in plastics: Migration, release, fate and environmental impact during their use, disposal and recycling. Journal of Hazardous Materials 344:179–99. doi: 10.1016/j.jhazmat.2017.10.014.
  • Haward, M. 2018. Plastic pollution of the world’s seas and oceans as a contemporary challenge in ocean governance. Nature Communications 9 (1):667. doi: 10.1038/s41467-018-03104-3.
  • Hee, Y. Y., K. Weston, and S. Suratman. 2022. The effect of storage conditions and washing on microplastic release from food and drink containers. Food Packaging and Shelf Life 32:100826. doi: 10.1016/j.fpsl.2022.100826.
  • Hernandez, L. M., E. G. Xu, H. C. E. Larsson, R. Tahara, V. B. Maisuria, and N. Tufenkji. 2019. Plastic teabags release billions of microparticles and nanoparticles into tea. Environmental Science & Technology 53 (21):12300–10. doi: 10.1021/acs.est.9b02540.
  • Hirt, N, and M. Body-Malapel. 2020. Immunotoxicity and intestinal effects of nano- and microplastics: A review of the literature. Particle and Fibre Toxicology 17 (1):57. doi: 10.1186/s12989-020-00387-7.
  • Huang, D., W. Zhou, S. Chen, J. Tao, R. Li, L. Yin, X. Wang, and H. Chen. 2022. Presence of polystyrene microplastics in cd contaminated water promotes cd removal by nano zero-valent iron and ryegrass (Lolium perenne L.). Chemosphere 303 (Pt 1):134729. doi: 10.1016/j.chemosphere.2022.134729.
  • Hüffer, T., A. K. Weniger, and T. Hofmann. 2018. Sorption of organic compounds by aged polystyrene microplastic particles. Environmental Pollution (Barking, Essex : 1987) 236:218–25. doi: 10.1016/j.envpol.2018.01.022.
  • Hwang, J., D. Choi, S. Han, J. Choi, and J. Hong. 2019. An assessment of the toxicity of polypropylene microplastics in human derived cells. The Science of the Total Environment 684:657–69. doi: 10.1016/j.scitotenv.2019.05.071.
  • Hwang, J., D. Choi, S. Han, S. Y. Jung, J. Choi, and J. Hong. 2020. Potential toxicity of polystyrene microplastic particles. Scientific Reports 10 (1):7391. doi: 10.1038/s41598-020-64464-9.
  • Iñiguez, M. E., J. A. Conesa, and A. Fullana. 2017. Microplastics in spanish table salt. Scientific Reports 7 (1):8620. doi: 10.1038/s41598-017-09128-x.
  • Jadhav, E. B., M. S. Sankhla, R. A. Bhat, and D. S. Bhagat. 2021. Microplastics from food packaging: An overview of human consumption, health threats, and alternative solutions. Environmental Nanotechnology, Monitoring & Management 16:100608. doi: 10.1016/j.enmm.2021.100608.
  • Jang, F. H., C. Wong, J. Choo, E. S. Aun Sia, A. Mujahid, and M. Müller. 2022. Increased transfer of trace metals and Vibrio sp. from biodegradable microplastics to catfish Clarias gariepinus. Environmental Pollution (Barking, Essex : 1987) 298:118850. doi: 10.1016/j.envpol.2022.118850.
  • Jenner, L. C., J. M. Rotchell, R. T. Bennett, M. Cowen, V. Tentzeris, and L. R. Sadofsky. 2022. Detection of microplastics in human lung tissue using ΜFTIR spectroscopy. The Science of the Total Environment 831:154907. doi: 10.1016/j.scitotenv.2022.154907.
  • Jin, Y., J. Xia, Z. Pan, J. Yang, W. Wang, and Z. Fu. 2018. Polystyrene microplastics induce microbiota dysbiosis and inflammation in the gut of adult zebrafish. Environmental Pollution (Barking, Essex : 1987) 235:322–9. doi: 10.1016/j.envpol.2017.12.088.
  • Ju, P., Y. Zhang, Y. Zheng, F. Gao, F. Jiang, J. Li, and C. Sun. 2020. Probing the toxic interactions between polyvinyl chloride microplastics and human serum albumin by multispectroscopic techniques. The Science of the Total Environment 734:139219. doi: 10.1016/j.scitotenv.2020.139219.
  • Kapukotuwa, R. W. M. G. K., N. Jayasena, K. C. Weerakoon, C. L. Abayasekara, and R. S. Rajakaruna. 2022. High levels of microplastics in commercial salt and industrial salterns in Sri Lanka. Marine Pollution Bulletin 174:113239. doi: 10.1016/j.marpolbul.2021.113239.
  • Karami, A., A. Golieskardi, Y. Bin Ho, V. Larat, and B. Salamatinia. 2017. Microplastics in eviscerated flesh and excised organs of dried fish. Scientific Reports 7 (1):5473. doi: 10.1038/s41598-017-05828-6.
  • Karami, A., A. Golieskardi, C. K. Choo, V. Larat, T. S. Galloway, and B. Salamatinia. 2017. The presence of microplastics in commercial salts from different countries. Scientific Reports 7 (1):46173. doi: 10.1038/srep46173.
  • Karami, A., A. Golieskardi, C. K. Choo, V. Larat, S. Karbalaei, and B. Salamatinia. 2018. Microplastic and mesoplastic contamination in canned sardines and sprats. The Science of the Total Environment 612:1380–6. doi: 10.1016/j.scitotenv.2017.09.005.
  • Karthik, R., R. S. Robin, R. Purvaja, D. Ganguly, I. Anandavelu, R. Raghuraman, G. Hariharan, A. Ramakrishna, and R. Ramesh. 2018. Microplastics along the beaches of southeast coast of India. Science of The Total Environment 645:1388–99. doi: 10.1016/j.scitotenv.2018.07.242.
  • Kedzierski, M., B. Lechat, O. Sire, G. le Maguer, V. Le Tilly, and S. Bruzaud. 2020. Microplastic contamination of packaged meat: Occurrence and associated risks. Food Packaging and Shelf Life 24:100489. doi: 10.1016/j.fpsl.2020.100489.
  • Kim, D., S. An, L. Kim, Y. M. Byeon, J. Lee, M.-J. Choi, and Y.-J. An. 2022. Translocation and chronic effects of microplastics on pea plants (Pisum sativum) in copper-contaminated soil. Journal of Hazardous Materials 436:129194. doi: 10.1016/j.jhazmat.2022.129194.
  • Kinigopoulou, V., I. Pashalidis, D. Kalderis, and I. Anastopoulos. 2022. Microplastics as carriers of inorganic and organic contaminants in the environment: A review of recent progress. Journal of Molecular Liquids 350:118580. doi: 10.1016/j.molliq.2022.118580.
  • Koelmans, A. A., N. H. M. Nor, E. Hermsen, M. Kooi, S. M. Mintenig, and J. de France. 2019. Microplastics in freshwaters and drinking water: Critical review and assessment of data quality. Water Research 155:410–22. doi: 10.1016/j.watres.2019.02.054.
  • Koelmans, A. A., P. E. Redondo-Hasselerharm, N. H. M. Nor, V. N. de Ruijter, S. M. Mintenig, and M. Kooi. 2022. Risk assessment of microplastic particles. Nature Reviews Materials 7 (2):138–52. doi: 10.1038/s41578-021-00411-y.
  • Kosuth, M., S. A. Mason, and E. V. Wattenberg. 2018. Anthropogenic contamination of tap water, beer, and sea salt. PloS One 13 (4):e0194970. doi: 10.1371/journal.pone.0194970.
  • Kumar, R., C. Manna, S. Padha, A. Verma, P. Sharma, A. Dhar, A. Ghosh, and P. Bhattacharya. 2022. Micro(nano)plastics pollution and human health: How plastics can induce carcinogenesis to humans? Chemosphere 298:134267. doi: 10.1016/j.chemosphere.2022.134267.
  • Kutralam-Muniasamy, G., F. Pérez-Guevara, I. Elizalde-Martínez, and V. C. Shruti. 2020. Branded milks – Are they immune from microplastics contamination? Science of The Total Environment 714:136823. doi: 10.1016/j.scitotenv.2020.136823.
  • Kwon, W., D. Kim, H. Y. Kim, S. W. Jeong, S. G. Lee, H. C. Kim, Y. J. Lee, M. K. Kwon, J. S. Hwang, J. E. Han, et al. 2022. Microglial phagocytosis of polystyrene microplastics results in immune alteration and apoptosis in vitro and in vivo. The Science of the Total Environment 807 (Pt 2):150817. doi: 10.1016/j.scitotenv.2021.150817.
  • Kwon, J. H., J. W. Kim, T. D. Pham, A. Tarafdar, S. Hong, S. H. Chun, S. H. Lee, D. Y. Kang, J. Y. Kim, S. bin Kim, et al. 2020. Microplastics in food: A review on analytical methods and challenges. International Journal of Environmental Research and Public Health 17 (18):6710–23. doi: 10.3390/ijerph17186710.
  • Lachenmeier, D., J. Kocareva, D. Noack, and T. Kuballa. 2015. Microplastic identification in German beer-an artefact of laboratory contamination? Deutsche Lebensmittel-Rundschau 111 (10):437–40. doi: 10.5281/zenodo.1250715.
  • Lee, H.-S., D. Amarakoon, C.-I. Wei, K. Y. Choi, D. Smolensky, and S.-H. Lee. 2021. Adverse effect of polystyrene microplastics (PS-MPs) on tube formation and viability of human umbilical vein endothelial cells. Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association 154:112356. doi: 10.1016/j.fct.2021.112356.
  • Lee, C.-H, and J. K.-H. Fang. 2022. The onset of surface-enhanced Raman scattering for single-particle detection of submicroplastics. Journal of Environmental Sciences 121:58–64. doi: 10.1016/j.jes.2021.08.044.
  • Lee, K.-W., W. J. Shim, O. Y. Kwon, and J.-H. Kang. 2013. Size-dependent effects of micro polystyrene particles in the marine copepod Tigriopus japonicus. Environmental Science & Technology 47 (19):11278–83. doi: 10.1021/es401932b.
  • Leslie, H. A., M. J. M. van Velzen, S. H. Brandsma, A. D. Vethaak, J. J. Garcia-Vallejo, and M. H. Lamoree. 2022. Discovery and quantification of plastic particle pollution in human blood. Environment International 163:107199. doi: 10.1016/j.envint.2022.107199.
  • Li, W., X. Chen, M. Li, Z. Cai, H. Gong, and M. Yan. 2022. Microplastics as an aquatic pollutant affect gut microbiota within aquatic animals. Journal of Hazardous Materials 423 (Pt B):127094. doi: 10.1016/j.jhazmat.2021.127094.
  • Liebezeit, G, and E. Liebezeit. 2013. Non-pollen particulates in honey and sugar. Food Additives & Contaminants. Part A, Chemistry, Analysis, Control, Exposure & Risk Assessment 30 (12):2136–40. doi: 10.1080/19440049.2013.843025.
  • Liebezeit, G, and E. Liebezeit. 2014. Synthetic particles as contaminants in German beers. Food Additives & Contaminants. Part A, Chemistry, Analysis, Control, Exposure & Risk Assessment 31 (9):1574–8. doi: 10.1080/19440049.2014.945099.
  • Liebezeit, G, and E. Liebezeit. 2015. Origin of synthetic particles in honeys. Polish Journal of Food and Nutrition Sciences 65 (2):143–7. doi: 10.1515/pjfns-2015-0025.
  • Li, D., Y. Shi, L. Yang, L. Xiao, D. K. Kehoe, Y. K. Gun’ko, J. J. Boland, and J. J. Wang. 2020. Microplastic release from the degradation of polypropylene feeding bottles during infant formula preparation. Nature Food 1 (11):746–54. doi: 10.1038/s43016-020-00171-y.
  • Lithner, D., Å. Larsson, and G. Dave. 2011. Environmental and health hazard ranking and assessment of plastic polymers based on chemical composition. The Science of the Total Environment 409 (18):3309–24. doi: 10.1016/j.scitotenv.2011.04.038.
  • Liu, Y., R. Guo, S. Zhang, Y. Sun, and F. Wang. 2022. Uptake and translocation of nano/microplastics by rice seedlings: Evidence from a hydroponic experiment. Journal of Hazardous Materials 421:126700. doi: 10.1016/j.jhazmat.2021.126700.
  • Liu, T., B. Hou, Z. Wang, and Y. Yang. 2022. Polystyrene microplastics induce mitochondrial damage in mouse GC-2 cells. Ecotoxicology and Environmental Safety 237:113520. doi: 10.1016/j.ecoenv.2022.113520.
  • Liu, G., J. Wang, M. Wang, R. Ying, X. Li, Z. Hu, and Y. Zhang. 2022. Disposable plastic materials release microplastics and harmful substances in hot water. The Science of the Total Environment 818:151685. doi: 10.1016/j.scitotenv.2021.151685.
  • Liu, L., M. Xu, Y. Ye, and B. Zhang. 2022. On the degradation of (micro)plastics: Degradation methods, influencing factors, environmental impacts. The Science of the Total Environment 806 (Pt 3):151312. doi: 10.1016/j.scitotenv.2021.151312.
  • Liu, Z., Q. Zhuan, L. Zhang, L. Meng, X. Fu, and Y. Hou. 2022. Polystyrene microplastics induced female reproductive toxicity in mice. Journal of Hazardous Materials 424 (Pt C):127629. doi: 10.1016/j.jhazmat.2021.127629.
  • Li, H., F. Wang, J. Li, S. Deng, and S. Zhang. 2021. Adsorption of three pesticides on polyethylene microplastics in aqueous solutions: Kinetics, isotherms, thermodynamics, and molecular dynamics simulation. Chemosphere 264 (Pt 2):128556. doi: 10.1016/j.chemosphere.2020.128556.
  • Li, J., D. Yang, L. Li, K. Jabeen, and H. Shi. 2015. Microplastics in commercial bivalves from China. Environmental Pollution (Barking, Essex : 1987) 207:190–5. doi: 10.1016/j.envpol.2015.09.018.
  • Li, X., T. Zhang, W. Lv, H. Wang, H. Chen, Q. Xu, H. Cai, and J. Dai. 2022. Intratracheal administration of polystyrene microplastics induces pulmonary fibrosis by activating oxidative stress and Wnt/β-catenin signaling pathway in mice. Ecotoxicology and Environmental Safety 232:113238. doi: 10.1016/j.ecoenv.2022.113238.
  • López, M. D., M. T. Toro, G. Riveros, M. Illanes, F. Noriega, M. Schoebitz, C. García-Viguera, and D. A. Moreno. 2022. Brassica sprouts exposed to microplastics: Effects on phytochemical constituents. The Science of the Total Environment 823:153796. doi: 10.1016/j.scitotenv.2022.153796.
  • Lozano, Y. M., T. Lehnert, L. T. Linck, A. Lehmann, and M. C. Rillig. 2021. Microplastic shape, polymer type, and concentration affect soil properties and plant biomass. Frontiers in Plant Science 12:1–14. doi: 10.3389/fpls.2021.616645.
  • Lu, L., T. Luo, Y. Zhao, C. Cai, Z. Fu, and Y. Jin. 2019. Interaction between microplastics and microorganism as well as gut microbiota: A consideration on environmental animal and human health. The Science of the Total Environment 667:94–100. doi: 10.1016/j.scitotenv.2019.02.380.
  • Luo, Y., C. Chuah, A. Amin, A. Khoshyan, C. T. Gibson, Y. Tang, R. Naidu, and C. Fang. 2022. Assessment of microplastics and nanoplastics released from a chopping board using raman imaging in combination with three algorithms. Journal of Hazardous Materials 431:128636. doi: 10.1016/j.jhazmat.2022.128636.
  • Luqman, A., H. Nugrahapraja, R. A. Wahyuono, I. Islami, M. H. Haekal, Y. Fardiansyah, B. Q. Putri, F. I. Amalludin, E. A. Rofiqa, F. Götz, et al. 2021. Microplastic contamination in human stools, foods, and drinking water associated with indonesian coastal population. Environments 8 (12):138. doi: 10.3390/environments8120138.
  • Lusher, A., P. Hollman, and J. Mendoza-Hill. 2017. Microplastics in Fisheries and Aquaculture: Status of Knowledge on Their Occurrence and Implications for Aquatic Organisms and Food Safety. Vol. 615 of FAO fisheries and aquaculture technicalpaper. 1 st ed. Rome: Food and Agriculture Organization of the United Nations.
  • Lu, L., Z. Wan, T. Luo, Z. Fu, and Y. Jin. 2018. Polystyrene microplastics induce gut microbiota dysbiosis and hepatic lipid metabolism disorder in mice. The Science of the Total Environment 631-632:449–58. doi: 10.1016/j.scitotenv.2018.03.051.
  • Lu, Y., Y. Zhang, Y. Deng, W. Jiang, Y. Zhao, J. Geng, L. Ding, and H. Ren. 2016. Uptake and accumulation of polystyrene microplastics in zebrafish (Danio rerio) and toxic effects in liver. Environmental Science & Technology 50 (7):4054–60. doi: 10.1021/acs.est.6b00183.
  • Madhumitha, C. T., N. Karmegam, M. Biruntha, A. Arun, A. A. al Kheraif, W. Kim, and P. Kumar. 2022. Extraction, identification, and environmental risk assessment of microplastics in commercial toothpaste. Chemosphere 296:133976. doi: 10.1016/j.chemosphere.2022.133976.
  • Manimozhi, N., V. Rani, C. Sudhan, D. Manimekalai, R. Shalini, and K. M. Abarna. 2022. Spatiotemporal occurrence, distribution, and characterization of microplastics in salt pans of the coastal region of the gulf of mannar, southeast coast of India. Regional Studies in Marine Science 53:102350. doi: 10.1016/j.rsma.2022.102350.
  • Marazuela, M. D., M. Klaiber, E. Moreno-Gordaliza, A. Barata, and M. M. Gómez-Gómez. 2022. Safety assessment of commercial antimicrobial food packaging: Triclosan and microplastics, a closer look. Food Packaging and Shelf Life 31:100780. doi: 10.1016/j.fpsl.2021.100780.
  • Mehrabi, R., A. H. Bahkali, K. A. Abd-Elsalam, M. Moslem, S. Ben M’barek, A. M. Gohari, M. K. Jashni, I. Stergiopoulos, G. H. J. Kema, and P. J. G. M. de Wit. 2011. Horizontal gene and chromosome transfer in plant pathogenic fungi a¡ecting host range. FEMS Microbiology Reviews 35 (3):542–54. doi: 10.1111/j.1574-6976.2010.00263.x.
  • Meng, X., J. Zhang, W. Wang, G. Gonzalez-Gil, J. S. Vrouwenvelder, and Z. Li. 2022. Effects of nano- and microplastics on kidney: Physicochemical properties, bioaccumulation, oxidative stress and immunoreaction. Chemosphere 288 (Pt 3):132631. doi: 10.1016/j.chemosphere.2021.132631.
  • Mohsen, M., C. Lin, S. Liu, and H. Yang. 2022. Existence of microplastics in the edible part of the sea cucumber Apostichopus japonicus. Chemosphere 287 (Pt 1):132062. doi: 10.1016/j.chemosphere.2021.132062.
  • Mu, Y., J. Sun, Z. Li, W. Zhang, Z. Liu, C. Li, C. Peng, G. Cui, H. Shao, and Z. Du. 2022. Activation of pyroptosis and ferroptosis is involved in the hepatotoxicity induced by polystyrene microplastics in mice. Chemosphere 291 (Pt 2):132944. doi: 10.1016/j.chemosphere.2021.132944.
  • Muthu, S. S. 2021. Chemical management in textiles and fashion. 1st ed. Cambridge: Woodhead Publishing.
  • Nienke Vrisekoop van UMC Utrecht onderzoekt gevaren van microplastics. 2019. Accessed July 5, 2022. https://utrecht.nieuws.nl/onderwijswetenschap/72826/nienke-vrisekoop-van-umc-utrecht-onderzoekt-gevaren-van-microplastics.
  • Novotna, K., L. Cermakova, L. Pivokonska, T. Cajthaml, and M. Pivokonsky. 2019. Microplastics in drinking water treatment – Current knowledge and research needs. The Science of the Total Environment 667:730–40. doi: 10.1016/j.scitotenv.2019.02.431.
  • Nowak, A, and I. Nowak. 2021. Review of harmful chemical pollutants of environmental origin in honey and bee products. Critical Reviews in Food Science and Nutrition :1–23. doi: 10.1080/10408398.2021.2012752.
  • O’Connor, J. D., H. T. Lally, A. A. Koelmans, A. M. Mahon, I. O’Connor, R. Nash, J. J. O’Sullivan, M. Bruen, L. Heerey, and S. Murphy. 2022. Modelling the transfer and accumulation of microplastics in a riverine freshwater food web. Environmental Advances 8:100192. doi: 10.1016/j.envadv.2022.100192.
  • Olewnik-Kruszkowska, E., A. Burkowska-But, I. Tarach, M. Walczak, and E. Jakubowska. 2020. Biodegradation of polylactide-based composites with an addition of a compatibilizing agent in different environments. International Biodeterioration & Biodegradation 147:104840. doi: 10.1016/j.ibiod.2019.104840.
  • Olewnik-Kruszkowska, E., J. Nowaczyk, and K. Kadac. 2016. Effect of ozone exposure on thermal and structural properties of polylactide based composites. Polymer Testing 56:299–307. doi: 10.1016/j.polymertesting.2016.10.030.
  • Olewnik-Kruszkowska, E., J. Nowaczyk, and K. Kadac. 2017. Effect of compatibilizig agent on the properties of polylactide and polylactide based composite during ozone exposure. Polymer Testing 60:283–92. doi: 10.1016/j.polymertesting.2017.04.009.
  • Oliveri Conti, G., M. Ferrante, M. Banni, C. Favara, I. Nicolosi, A. Cristaldi, M. Fiore, and P. Zuccarello. 2020. Micro- and nano-plastics in edible fruit and vegetables. The first diet risks assessment for the general population. Environmental Research 187:109677. doi: 10.1016/j.envres.2020.109677.
  • Oßmann, B. E., G. Sarau, H. Holtmannspötter, M. Pischetsrieder, S. H. Christiansen, and W. Dicke. 2018. Small-sized microplastics and pigmented particles in bottled mineral water. Water Research 141:307–16. doi: 10.1016/j.watres.2018.05.027.
  • Pan, Z., Q. Liu, J. Xu, W. Li, and H. Lin. 2022. Microplastic contamination in seafood from dongshan bay in southeastern china and its health risk implication for human consumption. Environmental Pollution (Barking, Essex : 1987) 303:119163. doi: 10.1016/j.envpol.2022.119163.
  • Periyasamy, A. P, and A. Tehrani-Bagha. 2022. A review on microplastic emission from textile materials and its reduction techniques. Polymer Degradation and Stability 199:109901. doi: 10.1016/j.polymdegradstab.2022.109901.
  • Peters, C. A., E. Hendrickson, E. C. Minor, K. Schreiner, J. Halbur, and S. P. Bratton. 2018. Pyr-GC/MS analysis of microplastics extracted from the stomach content of benthivore fish from the texas gulf coast. Marine Pollution Bulletin 137:91–5. doi: 10.1016/j.marpolbul.2018.09.049.
  • Pham, D. N., L. Clark, and M. Li. 2021. Microplastics as hubs enriching antibiotic-resistant bacteria and pathogens in municipal activated sludge. Journal of Hazardous Materials Letters 2:100014. doi: 10.1016/j.hazl.2021.100014.
  • Plastics and rubber products global market report 2022. 2022. Accessed July 5, 2022. https://www.globenewswire.com/news-release/2022/04/06/2417259/0/en/Plastics-And-Rubber-Products-Global-Market-Report-2022.html.
  • Prata, J. C. 2018. Airborne microplastics: Consequences to human health? Environmental Pollution (Barking, Essex: 1987) 234:115–26. doi: 10.1016/j.envpol.2017.11.043.
  • Prata, J. C., A. Paço, V. Reis, J. P. da Costa, A. J. S. Fernandes, F. M. da Costa, A. C. Duarte, and T. Rocha-Santos. 2020. Identification of microplastics in white wines capped with polyethylene stoppers using micro-Raman spectroscopy. Food Chemistry 331:127323. doi: 10.1016/j.foodchem.2020.127323.
  • Presence of microplastics and nanoplastics in food, with particular focus on seafood. 2016. Accessed July 7, 2022. https://doi.org/10.2903/j.efsa.2016.4501.
  • Qiao, R., Y. Deng, S. Zhang, M. B. Wolosker, Q. Zhu, H. Ren, and Y. Zhang. 2019a. Accumulation of different shapes of microplastics initiates intestinal injury and gut microbiota dysbiosis in the gut of zebrafish. Chemosphere 236:124334. doi: 10.1016/J.CHEMOSPHERE.2019.07.065.
  • Qiao, R., C. Sheng, Y. Lu, Y. Zhang, H. Ren, and B. Lemos. 2019b. microplastics induce intestinal inflammation, oxidative stress, and disorders of metabolome and microbiome in zebrafish. The Science of the Total Environment 662:246–53. doi: 10.1016/j.scitotenv.2019.01.245.
  • Qin, J., S. Zeng, X. Wang, and C. Lin. 2022. Generation of micro(nano)plastics and migration of plastic additives from poly(vinyl chloride) in water under radiation-free ambient conditions. Chemosphere 299:134399. doi: 10.1016/j.chemosphere.2022.134399.
  • Rainieri, S, and A. Barranco. 2019. Microplastics, a food safety issue? Trends in Food Science & Technology 84:55–7. doi: 10.1016/j.tifs.2018.12.009.
  • Rainieri, S., N. Conlledo, B. K. Larsen, K. Granby, and A. Barranco. 2018. Combined effects of microplastics and chemical contaminants on the organ toxicity of zebrafish (Danio rerio). Environmental Research 162:135–43. doi: 10.1016/j.envres.2017.12.019.
  • Rana, R., S. Joon, A. K. Jain, and N. Kumar Mohanty. 2020. A study on the effect of phthalate esters and their metabolites on idiopathic infertile males. Andrologia 52 (9):13720. doi: 10.1111/and.13720.
  • Ranjan, V. P., A. Joseph, and S. Goel. 2021. Microplastics and other harmful substances released from disposable paper cups into hot water. Journal of Hazardous Materials 404 (Pt B):124118. doi: 10.1016/j.jhazmat.2020.124118.
  • Ren, X., L. Wang, J. Tang, H. Sun, and J. P. Giesy. 2022. Combined effects of degradable film fragments and micro/nanoplastics on growth of wheat seedling and rhizosphere microbes. Environmental Pollution (Barking, Essex : 1987) 294:118516. doi: 10.1016/j.envpol.2021.118516.
  • Rillig, M. C., A. Lehmann, A. Abel de Souza Machado, and G. Yang. 2019. Microplastic effects on plants. The New Phytologist 223 (3):1066–70. doi: 10.1111/nph.15794.
  • Rochman, C. M., E. Hoh, T. Kurobe, and S. J. Teh. 2013. Ingested plastic transfers hazardous chemicals to fish and induces hepatic stress. Scientific Reports 3 (1):3263. doi: 10.1038/srep03263.
  • Rochman, C. M., J. M. Parnis, M. A. Browne, S. Serrato, E. J. Reiner, M. Robson, T. Young, M. L. Diamond, and S. J. Teh. 2017. Direct and indirect effects of different types of microplastics on freshwater prey (Corbicula fluminea) and their predator (Acipenser transmontanus). PloS One 12 (11):e0187664. doi: 10.1371/journal.pone.0187664.
  • Ruthsatz, K., M. Domscheit, K. Engelkes, and M. Vences. 2022. Microplastics ingestion induces plasticity in digestive morphology in larvae of Xenopus laevis. Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology 269:111210. doi: 10.1016/j.cbpa.2022.111210.
  • Sánchez, A., P. Rodríguez-Viso, A. Domene, H. Orozco, D. Vélez, and V. Devesa. 2022. Dietary microplastics: Occurrence, exposure and health implications. Environmental Research 212 (Pt A):113150. doi: 10.1016/j.envres.2022.113150.
  • Santana, M. F. M., F. T. Moreira, and A. Turra. 2017. Trophic transference of microplastics under a low exposure scenario: Insights on the likelihood of particle cascading along marine food-webs. Marine Pollution Bulletin 121 (1-2):154–9. doi: 10.1016/j.marpolbul.2017.05.061.
  • Schwabl, P., S. Köppel, P. Königshofer, T. Bucsics, M. Trauner, T. Reiberger, and B. Liebmann. 2019. Detection of various microplastics in human stool. Annals of Internal Medicine 171 (7):453–7. doi: 10.7326/M19-0618.
  • Schymanski, D., C. Goldbeck, H. U. Humpf, and P. Fürst. 2018. Analysis of microplastics in water by micro-raman spectroscopy: Release of plastic particles from different packaging into mineral water. Water Research 129:154–62. doi: 10.1016/j.watres.2017.11.011.
  • Senathirajah, K., A. Simon, B. Geetika, M. Carbery, S. Wilson, and T. Palanisami. 2021. Estimation of the mass of microplastics ingested – A pivotal first step towards human health risk assessment. Journal of Hazardous Materials 404 (Pt B):124004. doi: 10.1016/j.jhazmat.2020.124004.
  • Shi, H. 2021. Editorial overview: Microplastics in food and human exposure to microplastics. Current Opinion in Food Science 42:iii–v. doi: 10.1016/j.cofs.2021.11.009.
  • Shi, Y., P. Liu, X. Wu, H. Shi, H. Huang, H. Wang, and S. Gao. 2021. Insight into chain scission and release profiles from photodegradation of polycarbonate microplastics. Water Research 195:116980. doi: 10.1016/j.watres.2021.116980.
  • Shlush, E, and M. Davidovich-Pinhas. 2022. Bioplastics for food packaging. Trends in Food Science & Technology 125:66–80. doi: 10.1016/j.tifs.2022.04.026.
  • Shruti, V. C., F. Pérez-Guevara, I. Elizalde-Martínez, and G. Kutralam-Muniasamy. 2020. First study of its kind on the microplastic contamination of soft drinks, cold tea and energy drinks – Future research and environmental considerations. The Science of the Total Environment 726:138580. doi: 10.1016/j.scitotenv.2020.138580.
  • Shruti, V. C., F. Pérez-Guevara, I. Elizalde-Martínez, and G. Kutralam-Muniasamy. 2021. Toward a unified framework for investigating micro(nano)plastics in packaged beverages intended for human consumption. Environmental Pollution (Barking, Essex : 1987) 268 (Pt A):115811. doi: 10.1016/j.envpol.2020.115811.
  • Shruti, V. C., F. Pérez-Guevara, and G. Kutralam-Muniasamy. 2020. Metro station free drinking water fountain: A potential ‘microplastics hotspot’ for human consumption. Environmental Pollution (Barking, Essex : 1987) 261:114227. doi: 10.1016/j.envpol.2020.114227.
  • Sridhar, A., D. Kannan, A. Kapoor, and S. Prabhakar. 2022. Extraction and detection methods of microplastics in food and marine systems: A critical review. Chemosphere 286 (Pt 1):131653. doi: 10.1016/j.chemosphere.2021.131653.
  • Stock, V., L. Böhmert, G. Coban, G. Tyra, M. L. Vollbrecht, L. Voss, M. B. Paul, A. Braeuning, and H. Sieg. 2022. Microplastics and nanoplastics: Size, surface and dispersant – What causes the effect? Toxicology in Vitro : an International Journal Published in Association with BIBRA 80:105314. doi: 10.1016/j.tiv.2022.105314.
  • Sun, H., N. Chen, X. Yang, Y. Xia, and D. Wu. 2021. Effects induced by polyethylene microplastics oral exposure on colon mucin release, inflammation, gut microflora composition and metabolism in mice. Ecotoxicology and Environmental Safety 220:112340. doi: 10.1016/j.ecoenv.2021.112340.
  • Sun, R., K. Xu, L. Yu, Y. Pu, F. Xiong, Y. He, Q. Huang, M. Tang, M. Chen, L. Yin, et al. 2021. Preliminary study on impacts of polystyrene microplastics on the hematological system and gene expression in bone marrow cells of mice. Ecotoxicology and Environmental Safety 218:112296. doi: 10.1016/j.ecoenv.2021.112296.
  • Tagorti, G, and B. Kaya. 2022. Genotoxic effect of microplastics and COVID-19: The hidden threat. Chemosphere 286 (Pt 3):131898. doi: 10.1016/j.chemosphere.2021.131898.
  • Talbot, R, and H. Chang. 2022. Microplastics in freshwater: A global review of factors affecting spatial and temporal variations. Environmental Pollution (Barking, Essex : 1987) 292 (Pt B):118393. doi: 10.1016/j.envpol.2021.118393.
  • Tang, J., X. Ni, Z. Zhou, L. Wang, and S. Lin. 2018. Acute microplastic exposure raises stress response and suppresses detoxification and immune capacities in the scleractinian coral Pocillopora damicornis. Environmental Pollution (Barking, Essex : 1987) 243 (Pt A):66–74. doi: 10.1016/j.envpol.2018.08.045.
  • Tarasco, M., P. J. Gavaia, A. Bensimon-Brito, F. P. Cordelières, T. Santos, G. Martins, D. T. de Castro, N. Silva, E. Cabrita, M. J. Bebianno, et al. 2022. Effects of pristine or contaminated polyethylene microplastics on zebrafish development. Chemosphere 303 (Pt 3):135198. doi: 10.1016/j.chemosphere.2022.135198.
  • Teuten, E. L., J. M. Saquing, D. R. U. Knappe, M. A. Barlaz, S. Jonsson, A. Björn, S. J. Rowland, R. C. Thompson, T. S. Galloway, R. Yamashita, et al. 2009. Transport and release of chemicals from plastics to the environment and to wildlife. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 364 (1526):2027–45. doi: 10.1098/rstb.2008.0284.
  • Tian, L., C. Jinjin, R. Ji, Y. Ma, and X. Yu. 2022. Microplastics in agricultural soils: Sources, effects, and their fate. Current Opinion in Environmental Science & Health 25:100311. doi: 10.1016/j.coesh.2021.100311.
  • Tomazic-Jezic, V. J., K. Merritt, and T. H. Umbreit. 2001. Significance of the type and the size of biomaterial particles on phagocytosis and tissue distribution. Journal of Biomedical Materials Research 55 (4):523–9. doi: 10.1002/1097-4636(20010615)55:4<523::aid-jbm1045>3.0.co;2-g.
  • Tong, H., Q. Jiang, X. Hu, and X. Zhong. 2020. Occurrence and identification of microplastics in tap water from China. Chemosphere 252:126493. doi: 10.1016/j.chemosphere.2020.126493.
  • Toussaint, B., B. Raffael, A. Angers-Loustau, D. Gilliland, V. Kestens, M. Petrillo, I. M. Rio-Echevarria, and G. van den Eede. 2019. Review of micro-and nanoplastic contamination in the food Chain. Food Additives & Contaminants. Part A, Chemistry, Analysis, Control, Exposure & Risk Assessment 36 (5):639–73. doi: 10.1080/19440049.2019.1583381.
  • Vega-Herrera, A., M. Llorca, X. Borrell-Diaz, P. E. Redondo-Hasselerharm, E. Abad, C. M. Villanueva, and M. Farré. 2022. Polymers of micro(nano) plastic in household tap water of the barcelona metropolitan area. Water Research 220:118645. doi: 10.1016/j.watres.2022.118645.
  • Volkheimer, G. 1975. Hematogenous dissemination of ingested polyvinyl chloride particles. Annals of the New York Academy of Sciences 246 (1):164–71. doi: 10.1111/j.1749-6632.1975.tb51092.x.
  • Wang, F., J. Gao, W. Zhai, D. Liu, Z. Zhou, and P. Wang. 2020. The influence of polyethylene microplastics on pesticide residue and degradation in the aquatic environment. Journal of Hazardous Materials 394:122517. doi: 10.1016/j.jhazmat.2020.122517.
  • Wang, Y.-L., Y.-H. Lee, Y.-H. Hsu, I. J. Chiu, C. C.-Y. Huang, C.-C. Huang, Z.-C. Chia, C.-P. Lee, Y.-F. Lin, and H.-W. Chiu. 2021. The kidney-related effects of polystyrene microplastics on human kidney proximal tubular epithelial cells HK-2 and male C57BL/6 mice. Environmental Health Perspectives 129 (5):57003. doi: 10.1289/EHP7612.
  • Wang, T., C. Yu, Q. Chu, F. Wang, T. Lan, and J. Wang. 2020. Adsorption behavior and mechanism of five pesticides on microplastics from agricultural polyethylene films. Chemosphere 244:125491. doi: 10.1016/j.chemosphere.2019.125491.
  • Wang, W., J. Zhang, Z. Qiu, Z. Cui, N. Li, X. Li, Y. Wang, H. Zhang, and C. Zhao. 2022. Effects of polyethylene microplastics on cell membranes: A combined study of experiments and molecular dynamics simulations. Journal of Hazardous Materials 429:128323. doi: 10.1016/j.jhazmat.2022.128323.
  • Wang, C., J. Zhao, and B. Xing. 2021. Environmental source, fate, and toxicity of microplastics. Journal of Hazardous Materials 407:124357. doi: 10.1016/j.jhazmat.2020.124357.
  • Wiesheu, A. C., P. M. Anger, T. Baumann, R. Niessner, and N. P. Ivleva. 2016. Raman microspectroscopic analysis of fibers in beverages. Analytical Methods 8 (28):5722–5. doi: 10.1039/C6AY01184E.
  • Wu, C., K. Tanaka, Y. Tani, X. Bi, J. Liu, and Q. Yu. 2022. Effect of particle size on the colonization of biofilms and the potential of biofilm-covered microplastics as metal carriers. The Science of the Total Environment 821:153265. doi: 10.1016/j.scitotenv.2022.153265.
  • Wu, B., X. Wu, S. Liu, Z. Wang, and L. Chen. 2019. Size-dependent effects of polystyrene microplastics on cytotoxicity and efflux pump inhibition in human Caco-2 cells. Chemosphere 221:333–41. doi: 10.1016/j.chemosphere.2019.01.056.
  • Xi, B., B. Wang, M. Chen, X. Lee, X. Zhang, S. Wang, Z. Yu, and P. Wu. 2022. Environmental behaviors and degradation methods of microplastics in different environmental media. Chemosphere 299:134354. doi: 10.1016/j.chemosphere.2022.134354.
  • Xu, L., J. Liu, X. Yun Daphne Ma, Z. Li, C. He, and X. Lu. 2022. Facile anchoring mussel adhesive mimic tentacles on biodegradable polymer cargo carriers via self-assembly for microplastic-free cosmetics. Journal of Colloid and Interface Science 612:13–22. doi: 10.1016/j.jcis.2021.12.141.
  • Xu, K., Y. Zhang, Y. Huang, and J. Wang. 2021. Toxicological effects of microplastics and phenanthrene to zebrafish (Danio rerio). The Science of the Total Environment 757:143730. doi: 10.1016/j.scitotenv.2020.143730.
  • Yang, X., Y. B. Man, M. H. Wong, R. B. Owen, and K. L. Chow. 2022. Environmental health impacts of microplastics exposure on structural organization levels in the human body. The Science of the Total Environment 825:154025. doi: 10.1016/j.scitotenv.2022.154025.
  • Yang, D., H. Shi, L. Li, J. Li, K. Jabeen, and P. Kolandhasamy. 2015. Microplastic pollution in table salts from China. Environmental Science & Technology 49 (22):13622–7. doi: 10.1021/acs.est.5b03163.
  • Yang, D., J. Zhu, X. Zhou, D. Pan, S. Nan, R. Yin, Q. Lei, N. Ma, H. Zhu, J. Chen, et al. 2022. Polystyrene micro- and nano-particle coexposure injures fetal thalamus by inducing ros-mediated cell apoptosis. Environment International 166:107362. doi: 10.1016/j.envint.2022.107362.
  • Yin, K., Y. Wang, H. Zhao, D. Wang, M. Guo, M. Mu, Y. Liu, X. Nie, B. Li, J. Li, et al. 2021. A comparative review of microplastics and nanoplastics: Toxicity hazards on digestive, reproductive and nervous system. Science of The Total Environment 774:145758. doi: 10.1016/j.scitotenv.2021.145758.
  • Yuan, Z., R. Nag, and E. Cummins. 2022. Human health concerns regarding microplastics in the aquatic environment - from marine to food systems. Science of The Total Environment 823:153730. doi: 10.1016/j.scitotenv.2022.153730.
  • Zaheer, J., H. Kim, I. O. Ko, E.-K. Jo, E.-J. Choi, H.-J. Lee, I. Shim, H.-J. Woo, J. Choi, G.-H. Kim, et al. 2022. Pre/post-natal exposure to microplastic as a potential risk factor for autism spectrum disorder. Environment International 161:107121. doi: 10.1016/J.ENVINT.2022.107121.
  • Zhang, E., M. Kim, L. Rueda, C. Rochman, E. van Wormer, J. Moore, and K. Shapiro. 2022. Association of zoonotic protozoan parasites with microplastics in seawater and implications for human and wildlife health. Scientific Reports 12 (1):6532. doi: 10.1038/s41598-022-10485-5.
  • Zhang, W., Y. Tang, Y. Han, W. Zhou, W. Shi, S. Teng, P. Ren, G. Xiao, S. Li, and G. Liu. 2022. Microplastics boost the accumulation of tetrabromobisphenol a in a commercial clam and elevate corresponding food safety risks. Chemosphere 292:133499. doi: 10.1016/j.chemosphere.2021.133499.
  • Zhang, Y., S. Wang, V. Olga, Y. Xue, S. Lv, X. Diao, Y. Zhang, Q. Han, and H. Zhou. 2022. The potential effects of microplastic pollution on human digestive tract cells. Chemosphere 291 (Pt 1):132714. doi: 10.1016/j.chemosphere.2021.132714.
  • Zhang, J., L. Wang, L. Trasande, and K. Kannan. 2021. Occurrence of polyethylene terephthalate and polycarbonate microplastics in infant and adult feces. Environmental Science & Technology Letters 8 (11):989–94. doi: 10.1021/acs.estlett.1c00559.
  • Zhang, Z., S. Zhao, L. Chen, C. Duan, X. Zhang, and L. Fang. 2022. A review of microplastics in soil: Occurrence, analytical methods, combined contamination and risks. Environmental Pollution (Barking, Essex : 1987) 306:119374. doi: 10.1016/j.envpol.2022.119374.
  • Zhao, Y., R. Qiao, S. Zhang, and G. Wang. 2021. Metabolomic profiling reveals the intestinal toxicity of different length of microplastic fibers on zebrafish (Danio rerio). Journal of Hazardous Materials 403:123663. doi: 10.1016/j.jhazmat.2020.123663.
  • Zhou, X., G. Wang, X. An, J. Wu, K. Fan, L. Xu, C. Li, and Y. Xue. 2022. Polystyrene microplastic particles: In vivo and in vitro ocular surface toxicity assessment. Environmental Pollution (Barking, Essex: 1987) 303:119126. doi: 10.1016/j.envpol.2022.119126.
  • Zurier, H. S, and J. M. Goddard. 2021. Biodegradation of microplastics in food and agriculture. Current Opinion in Food Science 37:37–44. doi: 10.1016/j.cofs.2020.09.001.