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Presence of Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS) in Food Contact Materials (FCM) and Its Migration to Food

Ramírez Carnero , Arabela; Lestido Cardama, Antía; Vázquez Loureiro, Patricia; Barbosa Pereira, Letricia; Rodríguez Bernaldo de Quirós, Ana Isabel; Sendón García, Raquel

Abstract

Perfluoroalkyl and polyfluoroalkyl substances (PFAS) are synthetic chemical compounds widely used in different industry fields including food contact materials (FCM), providing resistance to fat and humidity, and non-stick properties. PFAS enter into the food chain directly from the intake of contaminated food or indirectly from the migration of the FCM into the food. This exposure published in different research highlights a public health concern. Therefore, it is necessary to perform analysis of the content of different FCM and evaluate the migration from the FCM under normal conditions of use and storage. This bibliographical review proves that different perfluoroalkyl and polyfluoroalkyl compounds are detected in fast food packaging, microwave popcorn bags, and frying pans, among others. Furthermore, it shows the conditions or factors that favor the migration of the PFAS from the FCM into the food

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foods Review Presence of Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS) in Food Contact Materials (FCM) and Its Migration to Food Arabela Ramírez Carnero, Antía Lestido-Cardama , Patricia Vazquez Loureiro , Letricia Barbosa-Pereira , Ana Rodríguez Bernaldo de Quirós and Raquel Sendón *   Citation: Ramírez Carnero, A.; Lestido-Cardama, A.; Vazquez Loureiro, P.; Barbosa-Pereira, L.; Rodríguez Bernaldo de Quirós, A.; Sendón, R. Presence of Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS) in Food Contact Materials (FCM) and Its Migration to Food. Foods 2021,10, 1443. https:// doi.org/10.3390/foods10071443 Academic Editor: Rafael Gavara Received: 24 May 2021 Accepted: 17 June 2021 Published: 22 June 2021 Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). Department of Analytical Chemistry, Nutrition and Food Science, Faculty of Pharmacy, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain; arabella.r[email protected] (A.R.C.); [email protected] (A.L.-C.); patriciavazquez.loureir[email protected] (P.V.L.); letricia.barbosa.per[email protected] (L.B.-P.); [email protected] (A.R.B.d.Q.) *Correspondence: [email protected]; Tel.: +34-881814964 Abstract: Perfluoroalkyl and polyfluoroalkyl substances (PFAS) are synthetic chemical compounds widely used in different industry fields including food contact materials (FCM), providing resistance to fat and humidity, and non-stick properties. PFAS enter into the food chain directly from the intake of contaminated food or indirectly from the migration of the FCM into the food. This exposure published in different research highlights a public health concern. Therefore, it is necessary to perform analysis of the content of different FCM and evaluate the migration from the FCM under normal conditions of use and storage. This bibliographical review proves that different perfluoroalkyl and polyfluoroalkyl compounds are detected in fast food packaging, microwave popcorn bags, and frying pans, among others. Furthermore, it shows the conditions or factors that favor the migration of the PFAS from the FCM into the food. Keywords: perfluoroalkyl substances; polyfluoroalkyl substances; perfluorooctanoic acid; perfluorosulfonic acid; food packaging; PTFAS migration 1. Introduction The perfluoroalkylated and polyfluoroalkylated substances (PFAS) are a series of synthetic chemical compounds formed by a hydrophobic alkyl chain of variable size (usually between 4 and 16 carbons), which can be partially or totally fluorinated, i.e., they contain one or more atoms of carbon in which the hydrogen atoms have been replaced by fluorine atoms and a final hydrophilic group [1]. In the case that the hydrophobic chain is partially fluorinated, they are called polyfluoroalkyl substances, while if the chain is totally fluorinated, except in the H atoms whose substitution would modify the nature of a functional group, they are called perfluoroalkyl substances. Polyfluoroalkyl substances can transform, under appropriate conditions, into perfluoroalkyl substances such as by degradation in the environment [2]. There are more than 4500 manufactured substances that meet the definition of PFAS, but only a few of these synthetic substances have been the object of study and legislation by the environmental and health authorities of different countries since both PFAS and their impurities are released into the environment in the production, use, and disposal processes. They are considered environmental pollutants and have been associated with different types of cancer, developmental toxicity, and immunotoxicity. For example, there are epidemiological studies linking exposure to long-chain perfluorooctanoic acid (PFOA) and/or perfluorooctane sulfonic acid (PFOS) with kidney and testicular cancer, low birth weight, thyroid disease, and immunotoxicity in children [3]. Foods 2021,10, 1443. https://doi.org/10.3390/foods10071443 https://www.mdpi.com/journal/foods Foods 2021,10, 1443 2 of 16 Most PFAS are acids that can be in their protonic or anionic form or even as a mixture of both. In the review of the terminology proposed by different authors, it was established to name all PFAS as acids instead of carboxylates, sulfonates, etc. [2]. Moreover, PFAS can be divided into two large groups: non-polymeric and polymeric PFAS, as shown in Figure 1. Foods 2021, 10, x FOR PEER REVIEW 2 of 16 Most PFAS are acids that can be in their protonic or anionic form or even as a mixture of both. In the review of the terminology proposed by different authors, it was established to name all PFAS as acids instead of carboxylates, sulfonates, etc. [2]. Moreover, PFAS can be divided into two large groups: non-polymeric and polymeric PFAS, as shown in Figure 1. Figure 1. Classification of perfluoroalkylated and polyfluoroalkylated substances [2]. 1. Non-polymeric perfluoroalkylated substances: 1.1. Perfluoroalkylated acids (PFAA) most representatives: 1.1.1. Perfluoroalkyl carboxylic acids (PFCAs), also known as perfluorocarboxylic acids or perfluoroalkanoic acids, have the general chemical formula CnF2n+1COOH. Some PFCAs are products of the abiotic or biotic degradation of certain PFAS. Perfluoroctanoic acid (PFOA) is the most frequently discussed compound (Figure 2). The ammonium salt, ammonium perfluorooctane (APFO), has been used in the production of fluoropolymers such as polytetrafluoroethylene (PTFE), commonly known as Teflon, which is used in kitchen utensils such as frying pans and pots due to its low coefficient of friction and its impermeability. Other acids are perfluorononanoic acid (PFNA), manufactured primarily for use as a fluorinated surfactant; perfluoroundecanoic acid (PFUnDA) and perfluorotridecanoic acid (PFTrDA) [2]. 1.1.2. Some perfluoroalkane sulfonic acids (PFSA) are perfluorobutane sulfonic acid (PFBS) and perfluorooctane sulfonic acid (PFOS) (Figure 2). PFOS has been Figure 1. Classification of perfluoroalkylated and polyfluoroalkylated substances [2]. 1. Non-polymeric perfluoroalkylated substances: 1.1. Perfluoroalkylated acids (PFAA) most representatives: 1.1.1. Perfluoroalkyl carboxylic acids (PFCAs), also known as perfluorocarboxylic acids or perfluoroalkanoic acids, have the general chemical formula C n F 2n+1 COOH. Some PFCAs are products of the abiotic or biotic degradation of certain PFAS. Perfluoroctanoic acid (PFOA) is the most frequently discussed compound (Figure 2). The ammonium salt, ammonium perfluorooctane (APFO), has been used in the production of fluoropolymers such as polytetrafluoroethylene (PTFE), commonly known as Teflon ® , which is used in kitchen utensils such as frying pans and pots due to its low coefficient of friction and its impermeability. Other acids are perfluorononanoic acid (PFNA), manufactured primarily for use as a fluorinated surfactant; perfluoroundecanoic acid (PFUnDA) and perfluorotridecanoic acid (PFTrDA) [2]. 1.1.2. Some perfluoroalkane sulfonic acids (PFSA) are perfluorobutane sulfonic acid (PFBS) and perfluorooctane sulfonic acid (PFOS) ( Figure 2 ). PFOS has been the most studied since it has been found in biota world- Foods 2021,10, 1443 3 of 16 wide. Besides, both PFOS and its salts have been classified as persistent, bioaccumulative, and toxic substances. Furthermore, it has been added to Annex B of the list of persistent organic contaminants of the Stockholm Convention, therefore its production and use is restricted [4]. 1.1.3. Perfluoroalkyl phosphonic and phosphinic acids (PFPAs and PFPIAs) are surfactants manufactured for a range of consumer and industrial uses. PFPAs have been widely detected in environmental waters. 1.2. Perfluoroalkane sulfonamide (PFASAs) such as perfluorooctane sulfonamide (PFOSA) is the major raw material for surfactant and surface protection products 1.3. Perfluoroalkyl iodide (PFAIs): It is a family of fluorotelomers whose degradation is a potential source of PFCA. One example is perfluorohexyl iodide (PFHxI), which chemical structure is C6F13I. Foods 2021, 10, x FOR PEER REVIEW 3 of 16 the most studied since it has been found in biota worldwide. Besides, both PFOS and its salts have been classified as persistent, bioaccumulative, and toxic substances. Furthermore, it has been added to Annex B of the list of persistent organic contaminants of the Stockholm Convention, therefore its production and use is restricted [4]. 1.1.3. Perfluoroalkyl phosphonic and phosphinic acids (PFPAs and PFPIAs) are surfactants manufactured for a range of consumer and industrial uses. PFPAs have been widely detected in environmental waters. 1.2. Perfluoroalkane sulfonamide (PFASAs) such as perfluorooctane sulfonamide (PFOSA) is the major raw material for surfactant and surface protection products 1.3. Perfluoroalkyl iodide (PFAIs): It is a family of fluorotelomers whose degradation is a potential source of PFCA. One example is perfluorohexyl iodide (PFHxI), which chemical structure is C 6 F 13 I. 2. Non-polymeric polyfluoroalkylated substances: 2.1. Perfluoroalkane sulfonamides, such as N-methylperfluorooctane sulfonamide (N-MeFOSA), N-ethyl perfluorobutane sulfonamide (EtFBSA), and N-butyl perflorooctane sulfonamide (BuFOSA). 2.2. Fluorotelomer substances: 2.2.1. Fluorotelomer alcohols of different chain lengths (FTOH) provide water and oil repellency and are used in materials in contact with food as non-stick agents. For example, 1H,1H,2H,2H-perfluorooctan-1-ol (6:2 FTOH), 1H,1H,2H,2H-perfluoro-decan-1-ol (8:2 FTOH) and 1H,1H,2H,2H-perfluoro-1- dodecanol (10:2 FTOH). In the “X:Y” designation used for naming fluorotelomer substances, X is the number of perfluorinated C atoms, while Y is the number of non-fluorinated C atoms that originate from the commercial synthesis. 2.2.2. Polyfluoroalkyl phosphoric acid esters, polyfluoroalkyl phosphates, and fluorotelomer phosphates (PAP) may be referred as polyalkyl phosphoric acid monoesters or fluorotelomer monophosphates (monoPAPs), and polyalkyl phosphoric acid diesters or fluorotelomer diphosphates (diPAPs). These compounds have been used as waterproofing agents for food contact paper [2]. Their approval as defoaming adjuvant in pesticide formulations has been rescinded [5]. Figure 2. Chemical structure of some PFAS. The carbon and fluorine bonds of these substances make them chemically stable, extremely resistant to degradation even at high temperatures, and resistant to water and oil. Therefore, perfluoroalkylated substances are widely used both in industry and in materials in contact with food, such as non-stick kitchen utensils and lipophobic and Figure 2. Chemical structure of some PFAS. 2. Non-polymeric polyfluoroalkylated substances: 2.1. Perfluoroalkane sulfonamides, such as N-methylperfluorooctane sulfonamide (N-MeFOSA), N-ethyl perfluorobutane sulfonamide (EtFBSA), and N-butyl perflorooctane sulfonamide (BuFOSA). 2.2. Fluorotelomer substances: 2.2.1. Fluorotelomer alcohols of different chain lengths (FTOH) provide water and oil repellency and are used in materials in contact with food as non-stick agents. For example, 1H,1H,2H,2H-perfluorooctan- 1-ol (6:2 FTOH), 1H,1H,2H,2H-perfluoro-decan-1-ol (8:2 FTOH) and 1H,1H,2H,2H-perfluoro-1-dodecanol (10:2 FTOH). In the “X:Y” designation used for naming fluorotelomer substances, Xis the number of perfluorinated C atoms, while Yis the number of non-fluorinated C atoms that originate from the commercial synthesis. 2.2.2. Polyfluoroalkyl phosphoric acid esters, polyfluoroalkyl phosphates, and fluorotelomer phosphates (PAP) may be referred as polyalkyl phosphoric acid monoesters or fluorotelomer monophosphates (monoPAPs), and polyalkyl phosphoric acid diesters or fluorotelomer diphosphates (diPAPs). These compounds have been used as waterproofing agents for food contact paper [ 2 ]. Their approval as defoaming adjuvant in pesticide formulations has been rescinded [5]. The carbon and fluorine bonds of these substances make them chemically stable, extremely resistant to degradation even at high temperatures, and resistant to water and oil. Therefore, perfluoroalkylated substances are widely used both in industry and in Foods 2021,10, 1443 4 of 16 materials in contact with food, such as non-stick kitchen utensils and lipophobic and hydrophobic coatings for paper and cardboard products. In addition, they are used in anti-stain coatings, waterproof fabrics, furniture paints and varnishes, fire extinguishing foams, and floor polishes due to their hydrophobic and lipophobic nature. High levels of PFAS, most commonly PFOS, PFHxA, PFOA, and PFDoA, have been found in ski waxes, leather samples, and carpets [ 6 ]. They are mainly used as raw materials for surfactants and surface protection products. PFAS bioaccumulate and pass the food chain through ingestion of contaminated food and beverages being the main route of direct exposure to PFAS. There is also an indirect exposure from consumption of foods that have been in contact with materials that had PFAS [7,8]. European Food Safety Authority (EFSA) collected monitoring data during the years 2000–2009 and in 2011 published a report on the presence of PFAS in 4881 samples collected in seven EU Member States. In this report, it was revealed that the highest mean contamination of PFOS (216 µ g kg −1 ), PFNA (10.3 µ g kg −1 ), PFOA (7.1 µ g kg −1 ), PFDA (6.0 µ g kg −1 ), and PFDoDA (3.7 µ g kg −1 ) was found in remains of game animals, mainly in the liver of wild pig. PFOS and PFOA were found sporadically in farm animals and poultry. In fish, PFOS and PFOSA were also found, with mean values of 47 and 15 µ g kg −1 , respectively. The concentrations of PFAS in farmed fish were lower than in wild fish, this could be due to contamination of rivers and seas by the industry that produces these substances. Shellfish are considered an important source of direct consumption of PFAS since there is a high frequency of positive results among them, although the number of samples analyzed is small [ 9 ]. Studies reveal that production of paper products may be a major PFAS point source, being an important vector for PFAS in the aquatic environment [10]. At the same time the European Commission published the Recommendation 2010/161/EU in which Member States must monitor the presence of perfluoroalkylated substances in food during 2010 and 2011. This surveillance had to include a wide variety of foods that reflected the eating habits of each region. Later, and due to their high persistence in the environment and the global distribution of these substances, the EFSA Technical Panel on Contaminants in the Food Chain (CONTAM) recommended collecting data on the presence of PFAS in different food products and the human body, especially evaluating the exposition [11]. After ingestion and excretion, fluorinated substances degraded end up in wastewater, so they are likely to further contaminate the environment and re-enter the food chain. Since the most frequent PFAS found in food samples are PFOS and PFOA, CONTAM established a tolerable daily intake (TDI) of 150 ng kg −1 body weight (bw) per day for PFOS and 1500 ng kg −1 bw per day for PFOA [ 11 ]. TDIs were based on a non-observed adverse effect level (NOAEL) of 0.03 mg kg −1 bw per day for PFOS and 0.06 mg kg −1 bw per day for PFOA. For the rest of PFAS found in food, there is no tolerable daily intake, and then dietary exposure studies are focused on these two substances. Chronic dietary exposure to the rest of PFAS is expected to be less than exposure to PFOA and PFOS. In the dietary exposure report published by EFSA in 2012, it was observed that in the case of PFOS, the estimates of dietary exposure were less than 3.5% of the TDI for average consumers and less than 6.7% of the TDI for high consumers, while in the case of PFOA, the exposure represented less than 0.3% for medium consumers and less than 0.5% for large consumers. Compared with the TDI established by the CONTAM, it can be observed that for both average and large consumers, the daily intake is below, with fish, shellfish, meat, and meat products being the main contributors to this exposure [11]. In eastern countries, the exposure is higher than in western countries, mainly because they have a higher contamination of the rivers used to irrigate rice crops, the basis of their diet. Exposure to PFAS in the population of Taiwan is 0.46 ng kg −1 bw per day for PFOS and 85.1 ng kg −1 bw per day for PFOA. In this country, the TDIs are exceeded in pregnant women due to the consumption of pork liver, which is not studied in Western countries because it is not a frequent food [12]. Foods 2021,10, 1443 5 of 16 It is important to note that migration of PFAS from FCM is not considered in the exposure calculations, possibly due to the lack of data. The objective of this work was to carry out a bibliographic review on perfluoroalkyl and polyfluoroalkyl substances to know both their presence in FCM and their migration data into food. 2. Legislation Materials that are intended to come into contact with food are regulated in the Regulation (EC) No. 1935/2004. This regulation establishes that materials and objects intended to extend the shelf life or maintain or improve the state of the food packaging must be manufactured following good manufacturing practices so that, under foreseeable conditions of use, they do not transfer their components in quantities that may represent a danger to human health, not causing the alteration of the organoleptic conditions of food or causing an unacceptable modification of its composition [13]. In 2010, PFOS was included in the Stockholm Convention, which is intended to control persistent organic pollutants to protect human health and the environment, so its use should be restricted as much as possible. In 2020, the EU published the Regulation (EU) 2020/784 that amends current EU legislation and restricts the use of persistent organic contaminants. The new regulation specifically limits the use of PFOA, its salts, and PFOA- related compounds. This regulation sets a maximum concentration of 0.025 mg kg −1 for PFOA and any of its salts, and a maximum concentration of 1 mg kg −1 for PFOA-related compounds or a combination of those compounds [ 14 ]. This was also taken into account when issuing the Commission Recommendation (EU) 2019/794, that recommends the investigation of the presence of PFAS in FCM, specifically its presence in paper and boardbased materials, such as those used to wrap fast food and takeaway and bakery products, and also popcorn bags [15]. 3. PFAS in Food Contact Materials Food contact materials (FCM) are materials intended to come in contact with food during its transport, storage, conservation, handling, or manufacture. Food packaging is used in the food industry to protect food from chemical, physical, and microbiological deterioration, which preserves the quality, nutritional and hygienic properties of the food, and in some cases, it even facilitates the processing of the food [16]. PFAS are widely used in FCM because its carbon-fluorine bonds provide high resistance to degradation even at high temperatures. FCM that contain PFAS, such as fast-food packaging and microwave popcorn bags or non-sticks utensils, can indirectly contribute to dietary exposure through the migration into food, which can be a food safety concern [ 3 ]. Consumption of restaurant food and popcorn was associated with higher serum levels of PFAS as a consequence of PFAS migration from the FCM [17]. FCM that contain perfluoroalkylated and polyfluoroalkylated substances can represent a health risk, since these can migrate into food and be ingested, and also being a risk to the environment, since they can be released in the process of eliminating these materials [18]. PFAS were first used in the 1940s and 1950s, and since then, they have been used in paper and cardboard packaging to provide resistance to water, oil, and fat. It is also a common practice to avoid the transfer of fats from the food to paper or cardboard packaging, improving its presentation. Since 1960, PFCAs have been used also as surfactants, such as PTFE (Polytetrafluoroethylene), which is used as a non-stick coating in pans or pots [ 19 ]. PTFE prevents food from sticking during the cooking process but also makes the utensil washing process easier. Both PFOS and PFOA are the most studied PFCAs since they have been found in higher concentrations in water, soil, and food [ 20 , 21 ]. Therefore, there are several studies of its presence in FCM, and they are summarized in Tables 1 and 2. The safety of fluorocarbon resins, including perfluoroalkyl and polyfluoroalkyl, such as PTFE, mostly known as Teflon ® , of pans and other kitchen utensils has been the aim of Foods 2021,10, 1443 6 of 16 some research studies, since these materials reach very high temperatures, which promote the migration. Analytical Determination PFAS, which are used in food contact paper and board, have been described to be highly persistent, bioaccumulative, and toxic. To determine the sources of PFAs exposure through paper and board, analytical methods are needed, not only to analyze them, but also their impurities and their degradation products. Consequently, new fluorinated products can appear, and there is currently no universal analysis methodology to identify all PFAs [ 22 ]. Polyfluorinated surfactants are complex mixtures that represents an analytical chance and require high performance analytical techniques to determine all the related substances that could be present in these FCM [23]. There are several non-specific methods to determine the total fluorine in samples. Spectroscopic methods can be used such as SSS (Sliding Spark Spectroscopy), NMR (Nuclear Magnetic Resonance), Raman spectroscopy, PIGE (particle-induced gamma-ray spectroscopy), or chromatographic methods such as CIC (Combustion Ion Chromatography with a conductivity detector), being PIGE and ion chromatography the most suitable quantitative methods to determine the amount of total organic fluorine in a sample [ 3 , 24 ]. In addition to this technique, Instrumental Neutron activation analysis (INAA) is another technique for total fluorine determination [25] As fluorine may be present in other fluorinated compounds or as inorganic fluorine, it is necessary to determine PFAS. The identification of these types of compounds is difficult since they are present in low concentrations, and the samples usually contain a mixture of different types of PFAS [26]. The results obtained are usually expressed as analyte weight/material surface or transformed in analyte weight/food or simulant weight considering that 1 kg of food is generally in contact with 6 dm2of material (or the real relationship if it is known), also as analyte weight/material weight [27]. The determination of the content in the materials is usually performed by liquid chromatography (LC or UPLC) coupled to a mass spectrometry (MS) detector. Tandem mass spectrometry is also employed [28–31]. Some laboratories in Denmark and Sweden have established liquid chromatography coupled to mass spectrometry (LC-MS) as a method to determine PFAA, some derivatives of PFOS, and total organic fluorine [22]. Liquid chromatography methods coupled to triple quadrupole mass spectrometry (LC-QqQ) and coupled to quadrupole time-of-flight mass spectrometry (LC-QTOF) have been developed, both LC/MS-MS based techniques can detect PFAS at lower levels in the packaging [32,33]. Fluorinated compounds are intentionally added to materials that are in direct contact with food. Paper samples were analyzed by Shaider et al. (2017) and total fluorine was not detected in samples that were not intended for food contact, while in those designed for food contact, fluorine was found to be higher than 16 nmol cm−2[3]. Microwave popcorn packaging has been highly studied since they are subjected to high temperatures during their preparation and are used into contact with fatty acids. In the study of Monge Brenes et al. (2019) several works that study the presence of the most monitored perfluoroalkylated substances, both PFAS and PFOS, in this type of packaging between 2005 and 2018 are included and further commented below. The results of this study suggest a reduction in the concentration of PFOS and PFOA in microwave packaging [ 34 ]. Dolman et al. (2011) detected PFOA in a popcorn bag, as well as other PFCs such as PFHxA, PFHpA, PFNA, PFDA, and PFUA, showing that popcorn bags were treated with PFC to increase their resistance to temperature and fats. In this case, after using the microwave, no PFCs were detected in the popcorn, suggesting that the PFCs remained in the bag and therefore did not migrate to the popcorn [35]. Foods 2021,10, 1443 7 of 16 Granby et al. (2018) carried out a similar study in the Technical University of Denmark, in which three samples of popcorn bags were analyzed. Among the 35 samples analyzed, including baking dishes, fast-food packaging, popcorn bags, and muffin packaging, the presence of different types of PFAS was detected in 13 samples. The sum of the different PFCAs (PFPeA, PFHxA, PFHpA, PFOA, PFNA, PFDA, PFUnDA, PFDoDA, PFTeA, PFTrA) detected in 10 samples ranged between 0.01 and 13.1 µ g kg −1 of food. Fluorotelomer alcohols (FTOH) were detected in nine samples at concentrations of 0.8–13.5 µ g kg −1 of food, 6:2 FTOH being the most frequently detected as well as the one with higher concentration quantified in each sample. The highest concentrations of PFAS (PFCA and FTOH) were detected in two muffin packaging with values of 6.1 and 14.1 µ g kg −1 , respectively, and in three baking dishes with values of 19.4, 13.3, and 25.3 µ g kg −1 , respectively. Migration tests were also carried out on these five samples [29]. The standards employed are not the same in western countries as in eastern countries. In American and European countries, shorter-chain PFCAs, PFBA, PFPeA, PFHxA are used, while in Asian countries, especially in China, longer chain PFCAs, PFOA, PFNA, PFDA are used [36]. Yuan et al. (2016) analyzed 42 samples of food packaging made of paper and aluminum, including fast-food wrappers, popcorn packaging, pizza and sandwich boxes, baking paper and aluminum wrappers. They used pressurized liquid extraction (PLE) followed by LC-MS/MS and the isotope dilution method to quantify determine 12 PFCs: PFBA, PFPeA, PFHxA, PFHpA, PFOA, PFNA, PFDA, PFUnDA, PFDoA, PFBS, PFHxS, and PFOS and 5 PFCs: PFTrDA, PFTeDA, PFHxDA, PFoDA, and PFD. PFHxA was detected in a cup of ice cream, PFBA, PFHxA, PFHpA, PFNA, PFDA, and PFDoA were detected in fast-food wrappers, while the highest values were obtained in bags of microwave popcorn. In this case, neither PFOA nor PFOS were significantly detected, unlike those that occurred in the European studies mentioned before [28]. The same researchers previously mentioned compared the presence of FTOH; both 6:2 FTOH, 8:2 FTOH and 10:2 FTOH, 12:2 FTOH, 14:2 FTOH, 16:2 FTOH, and 18:2 FTOH were found in eco-friendly paper tableware, microwave popcorn bags, and other FCM such as packaging for cupcakes, cups, and cardboard boxes. It was also observed that the mean concentration of the total FTOH was higher in ecological paper tableware (2990 µ g kg −1 ) than in other FCM (<0.55–38.7 µ g kg −1 ) but lower than those present in the microwave paper (18,200 µg kg−1) [12]. No scientific research is available on possible PFAS contamination of paper and board FCMs when contaminated process water is used in the manufacture of paper since PFAS are ubiquitous in the environment. Some studies that determine PFAS in FCM are shown in Table 1. Table 1. Determination of PFAS content in FCM. Country Compound Type of Sample Origin of Sample Method of Determination Concentration Reference Australia PFOA PFHxA PFHpA PFNA PFDA PFUA Popcorn bags, baking paper, box of chips, sandwich wrap, hamburger box Local shops and fast-food restaurants LC-MS PFOA: 9.1 ×106g kg−1[35] EEUU PFOA PTFE cookware, popcorn bags, PTFE film/sealant tape. Not specified LC-MS LC-MS/MS 4–290 µg kg−1 PTFE film/sealant tape: 1800 µg kg−1[37] Foods 2021,10, 1443 8 of 16 Table 1. Cont. Country Compound Type of Sample Origin of Sample Method of Determination Concentration Reference EEUU PFOA PFOS Bags of popcorn, sandwich bags Not specified UHPLC-QTOF PFOS < LOD PFOA: 22.1 and 12.9 ng dm−2[34] Denmark PFCA PFSA PAPs FTOH Baking paper, fast-food packaging, boxes of pizza, popcorn bags, etc. Distributors and retailers in Norway LC-MS/MS FTOH: 1.3 µg kg−1 of food [29] Greece PFBA PFPeA PFHxA PFHpA PFOA PFNA PFDA PFUnDA PFDoA PFTrDA PFTeDA PFHxDA PFODA PFBS PFHxS PFOS PFDS Fast-food packaging, sandwiches, cups, ice cream containers, baking paper, popcorn bags, etc. Athens market and fast-food restaurants in Greece. PLE, LC-MS/MS PFBA: 275.84 µg kg−1 PFHxA: 341.21 µg kg−1 PFHpA: 5.19 µg kg−1 [38] China 6:2 FTOH 8:2FTOH 10.2 FTOH 12:2 FTOH 14:2 FTOH 16:2 FTOH 18:2 FTOH Bags of popcorn, materials labelled as ecological, cupcake packaging, etc. Beijing retail market and online UPLC-MS/MS UPLC-QTOF Average concentration of total FTOH: 2990 µg kg−1 [28] 4. PFAS Migration into Food FCMs can transfer substances to food through a process known as migration. Migration is a phenomenon that cannot be avoided, and it depends on many factors that obey Fick’s laws of diffusion. This migration depends on the facility of PFAS to be released by the material, on the food contact conditions such as temperature and exposure time, on the properties of the material in contact with food such as thickness, initial concentration, and diffusion coefficient, and on the interaction between the material and the compound, expressed as the coefficient of distribution between the material and the food [22,39]. Furthermore, the extent of migration to food depends on the concentration, mass fractions, type, and length of the PFAS chain, as well as the nature of food while the migration increases with the use of high temperatures and the use of fats even if the contact time between the material and the food is short [3,40]. The ingestion of this type of substances is a food safety problem, so it is necessary to evaluate the migration of PFAS from FCM into the food in usual conditions of cooking and storage. The first step is the release of PFAS from the surface of the material, which depends on whether PFAS is absorbed into the material or on the material surface. For the release of these substances, the surface should be wet and break the bonds between the substance and the surface [ 22 , 28 ]. The second step for the migration of PFAS is the dissolution of the compounds into food. Foods 2021,10, 1443 9 of 16 The determination of PFAS in food is difficult because the food can have this type of chemical substances before its packaging or processing, since they are environmental pollutants. To carry out these migration tests, it is advisable to use food simulants since they are simpler analytical matrices than food [41]. Furthermore, it is necessary to ensure that there is no contamination from the material laboratory used. Some studies replace, for example, the PTFE filter used at the entry of the mobile phase in LC-MS with a paper filter free of Teflon [30]. Migration tests were carried out under the following conditions: for example, in the case of a dish which contains food to be heated in a microwave, the migration conditions used were 70 ◦ C for 2 h, since it is expected to reach high temperatures during food preparation [ 29 ]. In the case of samples such as baking paper that cannot contain liquids, a part of the sample is embedded in the lid of a stainless-steel cylinder, in which a simulant such as Tenax ® is used for solid foods and seal before introducing them in the oven at a suitable temperature and time [ 30 ]. For samples such as muffin wrappers, pizza boxes, and cups for hot drinks, square cuts of them are made before adding the simulant and placing them at the appropriate temperature for the time necessary for migration to occur [29], as established by the Commission Regulation (EU) No 10/2011 [16]. 4.1. PFAS Migration Levels and Food 4.1.1. Fat Content PFAS are mostly found in foods rich in proteins, such as liver, game meat, farm animals, and fish because of the easier union with this essential nutrient [ 9 ]. However, in the migration tests, the fat content affects more than the protein content since these substances are used to increase the resistance of the material to fats, being widely used in fast-food packaging and ultra-processed foods. Begley et al. (2005) used a PTFE sealant film with a high content of PFOA as surrogate to compare the migration after 2h in water at 100 ◦ C and Myglyol at 100 and 175 ◦ C. In the migration test at 100 ◦ C higher levels of PFOA were determined (150 ng dm −2 vs. 120 ng dm−2 ), but in the case of Myglyol at 175 ◦ C the quantity of PFOA was higher than in the two previous cases (710 ng dm−2) [37]. Choi et al. (2018) analyzed a total of 312 samples, including pans, bakeware, electric rice cookers, grills, and baking papers, showing that PFAS do not migrate equally to all types of food. In this case, the analytes that migrated in the highest proportion were PFODA with a concentration of 3.05 µ g L −1 in the n-heptane simulant and PFNA with a concentration of 2.12 µ g L −1 in 50% ethanol, simulant in which these compounds are most frequently detected. These results indicate that the migration of PFCs is more likely in alcoholic beverages or into fatty foods [30]. Elizalde et al. (2018) have studied the migration of perfluorinated compounds from paper bags to Tenax ® and lyophilized milk and concluded that migration of PFHxA, PFHpA, PFOA, PFNA, PFDA, PFTrDA, and PFTeDA was higher in whole milk than in low-fat milk. Both kinds of milk were freeze-dried, and low-fat milk contained 50% less fat than whole milk [31]. In the case of emulsified foods, higher migration levels are shown compared to nonemulsified fatty foods. The migration of PFAS in emulsified foods studied by Begley et al. (2008) showed that it was up to 50 times higher in emulsified foods, such as butter, compared to the migration in non-emulsified fats, such as oil. This effect was the same in the migration using food simulants, where increasing the percentage of ethanol with respect to water, from 10% to 30%, implies an increase in the migration of PFAS at 100 ◦C [42]. 4.1.2. Moisture Content The degree of moisture of food also affects the migration of PFAS to food. Fengler et al. (2011) compared the migration in two samples of muffin masses, one of them was drier than the other. It was observed that in the case of the sample with higher moisture content, the FTOH values were lower than in the case of the muffin with lower moisture Foods 2021,10, 1443 16 of 16 32. Moreta, C.; Tena, M.T. Fast Determination of Perfluorocompounds in Packaging by Focused Ultrasound Solid-Liquid Extraction and Liquid Chromatography Coupled to Quadrupole-Time of Flight Mass Spectrometry. J. Chromatogr. A 2013 ,1302, 88–94. [CrossRef] 33. Moreta, C.; Tena, M.T. Determination of Perfluorinated Alkyl Acids in Corn, Popcorn and Popcorn Bags before and after Cooking by Focused Ultrasound Solid–Liquid Extraction, Liquid Chromatography and Quadrupole-Time of Flight Mass Spectrometry. J. Chromatogr. A 2014,1355, 211–218. [CrossRef] 34. Monge Brenes, A.L.; Curtzwiler, G.; Dixon, P.; Harrata, K.; Talbert, J.; Vorst, K. PFOA and PFOS Levels in Microwave Paper Packaging between 2005 and 2018. Food Addit. Contam. Part B 2019,12, 191–198. [CrossRef] 35. Dolman, S.; Pelzing, M. An Optimized Method for the Determination of Perfluorooctanoic Acid, Perfluorooctane Sulfonate and Other Perfluorochemicals in Different Matrices Using Liquid Chromatography/Ion-Trap Mass Spectrometry. J. Chromatogr. B 2011,879, 2043–2050. [CrossRef] 36. Zabaleta, I.; Negreira, N.; Bizkarguenaga, E.; Prieto, A.; Covaci, A.; Zuloaga, O. Screening and Identification of Per- and Polyfluoroalkyl Substances in Microwave Popcorn Bags. Food Chem. 2017,230, 497–506. [CrossRef] 37. Begley, T.H.; White, K.; Honigfort, P.; Twaroski, M.L.; Neches, R.; Walker, R.A. Perfluorochemicals: Potential Sources of and Migration from Food Packaging. Food Addit. Contam. 2005,22, 1023–1031. [CrossRef] 38. Zafeiraki, E.; Costopoulou, D.; Vassiliadou, I.; Bakeas, E.; Leondiadis, L. Determination of Perfluorinated Compounds (PFCs) in Various Foodstuff Packaging Materials Used in the Greek Market. Chemosphere 2014,94, 169–176. 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Migration of Fluorinated Telomer Alcohols (FTOH) from Food Contact Materials into Food at Elevated Temperatures. Organohalogen Compd. 2011,73, 939–942. 44. AbulFadl, M.M.; Sharaf, A.M.; Mostafa, M.M.; El-Saeid, M.H. Impact of Household Cooking on Release of Fluorinated Compounds PFOA and PFOS from Tefal Coated Cookware to Foods. World J. Adv. Res. Rev. 2019,3, 024–030. [CrossRef] 45. WHO. Salt Reduction. 2020. Available online: https://www.who.int/news-room/fact-sheets/detail/salt-reduction (accessed on 29 April 2020).