Consumer exposure to phthalates from paper packaging: an integrated approach

This paper presents an integrated approach to estimate the exposure of the Portuguese population to phthalates as a contaminant originating from paperboard packaging. The approach combined data of migrant concentration in the foods resulting from a stochastic simulation with consumption data of food packaged in paperboard. The results from the exposure model were validated with experimental values actually found in the food. A short surveillance exercise was conducted with samples collection from market shelves to identify and quantify the phthalates present in both the packages and the food. The distribution of values for the di-butyl phthalate concentration in the packages was used as the input of the initial concentration in the Weibull model to estimate the concentration of this phthalate in the foods. This distribution of occurrence data was then combined with the packaging usage data in a probabilistic simulation with a Monte Carlo sampling method. Exposure values ranged between zero and 8.95 µg day^?1 kg_bw, a value close to the tolerable daily intake established by the European Food Safety Authority (EFSA)–10 µg day^?1 kg_bw. However, the 97.5th percentile and the average were 1.82 and 0.44 day^?1 kg_bw, respectively, indicating that further refinement of the estimates is not necessary. Other phthalates were also detected in the packaging samples: di-isobutyl phthalate and di-ethylhexyl phthalate. The latter was present in all packaging samples collected and was detected in a few food samples at values requiring further investigation.     

Determination of phthalates in raw bovine milk by gas chromatography/time-of-flight mass spectrometry (GC/TOF-MS) and dietary intakes

Low levels of phthalates, including di(2-ethylhexyl) phthalate (DEHP), in raw bovine milk were determined using gas chromatography/time-of-flight mass spectrometry (GC/TOF-MS). A fast and convenient process of sample treatment combined with TOF-MS analysis (medium resolution >5000), yielded good recoveries (85–125%) and low limits of detection (<0.002 mg kg^?1). The most commonly used phthalate, DEHP, was found in 15 out of 30 samples monitored in this study. DEHP concentrations in raw milk ranged from not detected to 0.154 mg kg^?1, and the mean concentration was 0.057 mg kg^?1. The dietary intake of DEHP was about 0.004 mg kg^?1 body weight day^?1 if a child (24 months, 13 kg body weight) drinks 1 L day^?1 of milk that contains the mean concentration of DEHP found in raw milk. The estimated dietary intake corresponded to 8% of the European Union tolerable daily intake (TDI) of 0.05 mg kg^?1 body weight day^?1. Dimethyl phthalate (DMP) and di-n-butyl phthalate (DBP) were found from two and 20 samples, respectively, at low levels. Diethyl phthalate (DEP), butylbenzyl phthalate (BBP), and di-n-octyl phthalate (DnOP) were not found in any of the samples.     

Mycotoxins,trace elements,and phthalates in marketed rice of different origin and exposure assessment

ABSTRACT

The aim of this study was to determine levels of 11 mycotoxins, 10 trace elements, and 6 phthalates in rice samples from Serbian and Chinese market. Mycotoxins were not detected in any of the analysed rice samples. Results revealed similar median levels for following elements: Mn, 17.5 and 15.7 mg kg^?1; Fe, 2.47 and 2.12 mg kg^?1; Cu, 1.95 and 1.59 mg kg^?1 in marketed samples from Serbia and China, respectively. Median concentration of Ni in Serbian marketed samples was 1.9 times higher than in Chinese ones. The median levels (µg kg^?1) of phthalates ranged from 1.2 (benzylbutyl phthalate [BBP]) – 566 (di(2-ethyl-hexyl) phthalate [DEHP]) and 1.7 (BBP) – 348 (DEHP) in Serbian and Chinese marketed samples, respectively. The results were used to assess daily exposure of Serbian and Chinese adult consumers. The calculated target hazard quotients indicated that the potential risk attributable to the analysed contaminants in rice samples should not be of concern neither for the Serbian nor the Chinese consumers.     

Migration of epoxidized soybean oil (ESBO) and phthalates from twist closures into food and enforcement of the overall migration limit

Nineteen samples of food in glass jars with twist closures were collected by the national food inspectors at Danish food producers and a few importers, focusing on fatty food, such as vegetables in oil, herring in dressing or pickle, soft spreadable cheese, cream, dressings, peanut butter, sauces and infant food. The composition of the plasticizers in the gaskets was analysed by gas chromatography with flame ionization detection (GC-FID) and gas chromatography-mass spectrometry (GC-MS). Epoxidized soybean oil (ESBO) and phthalates were determined in the homogenized food samples. ESBO was the principal plasticizer in five of the gaskets; in 14 it was phthalates. ESBO was found in seven of the food samples at concentrations from 6 to 100 mg kg^?1. The highest levels (91–100 mg kg^?1) were in oily foods such as garlic, chilli or olives in oil. Phthalates, i.e. di-iso-decylphthalate (DIDP) and di-iso-nonylphthalates (DINP), were found in seven samples at 6–173 mg kg^?1. The highest concentrations (99–173 mg kg^?1) were in products of garlic and tomatoes in oil and in fatty food products such as sauce béarnaise and peanut butter. For five of the samples the overall migration from unused lids to the official fatty food simulant olive oil was determined and compared with the legal limit of 60 mg kg^?1. The results ranged from 76 to 519 mg kg^?1 and as a consequence the products were withdrawn from the market.     

Quantitative analysis of styrene monomer in foods. A limited East Australian Survey

The levels of styrene monomer in foods packaged in polystyrene containers were determined by a headspace gas chromatography (g.c.) method and two reversed phase high-performance liquid chromatography (h.p.l.c.) methods. A total of 146 samples were analysed from Victoria and New South Wales which included yoghurt, cream, cheese, dessert, ice cream, egg white, onion dip and margarine. The highest level of styrene found was 0.1 mg kg^?1 in yoghurt. About 85% of all yoghurt samples were found to have values less than 0.05 mg kg^?1. The lowest values of styrene obtained were for margarine samples, of which more than 90% contained less than 0.010 mg kg^?1. The estimated limits of detection of the h.p.l.c. methods for all products except margarine were 0.005 mg kg^?1. The h.p.l.c. detection limit for margarine and the g.c. method for yoghurt were estimated to be 0.01 mg kg^?1.     

Occurrence and infant exposure assessment of nitrates in baby foods marketed in the region of Lisbon,Portugal

Commercial baby food labelled as from organic or conventional origin, including vegetable-based baby foods, fruit purees and fruit juices (n?=?80), were analysed for nitrate content by an in-house validated HPLC method. Nitrate contents ranged from 5 to 230?mg?kg^?1 with a mean concentration of 102?mg?kg^?1 for vegetable-based baby foods, and a median of 5?mg?kg^?1 for both fruit purees and juices. One sample of vegetable-based baby food was higher than the legislated value (200?mg?kg^?1). There were no significant differences between average nitrate levels in analysed samples regarding both farming systems. The estimated nitrate intake through baby foods for a mean nitrate concentration of 47?mg?kg^?1 ranged between 0.5 (15% of ADI) and 1.3?mg?kg^?1?bw?day^?1 (35% of ADI). The ADI level was exceeded (107–146% of ADI) only for the 95th and 99th percentiles of nitrate concentration.     

Boron concentrations in selected foods from borate‐producing regions in Turkey

As part of a large‐scale programme to investigate the health effects of exposure to borate minerals in Turkey, boron concentrations in vegetables, fruits and some other foods were determined. From all borate‐producing regions of the country, 22 species of fruit, 17 species of vegetable, 12 species of cereal, legume and oilseed, three species of herbs and six types of other food were collected in 1999 and analysed for boron concentrations using the Azomethine H method. The results were compared with 37 types of food collected from areas well distant from the borate‐producing areas. The total number of samples evaluated was 420. Pistachio (67.0 mg kg^?1) had the highest concentration of boron, followed by grape leaf (60.48 mg kg^?1), sour cherry (57.03 mg kg^?1), quince (38.78 mg kg^?1), peach (34.49 mg kg^?1), grape (20.70 mg kg^?1), green beans (19.49 mg kg^?1), unripe peach (18.92 mg kg^?1) and parsley (10.24 mg kg^?1) from the borate‐producing regions. A large number of foods contained boron at higher concentrations than those reported in the literature, most probably due to the high boron content of these Turkish soils. According to the results of t‐tests, the area itself does not have a significant effect (p > 0.05) on boron concentration in all foods evaluated so far. Copyright © 2003 Society of Chemical Industry     

Survey of sulfites in wine and various Turkish food and food products intended for export, 2007–2010

Surveys were carried out between 2007 and 2010 to determine the total levels of sulfites in 1245 samples of wines, dried apricots, dried vegetables, nuts, juices and purees, frozen foods and cereals containing dried fruit supplied by food inspectors and by food producers for testing or for export certification. Sulfite analysis of wine was carried out using the Ripper method with an LOQ of 5?mg?l^?1 and for dried and other foods the Monier-Williams distillation procedure was employed with an LOQ of 10?mg?kg^?1. In the survey all wines contained measurable sulfites, but with the exception of one sample of white wine they were otherwise below Turkish Food Codex limits of 160?mg?kg^?1 for red wine, 210?mg?kg^?1 to white wine and 235?mg?kg^?1 for sparkling wine. None of the cereal products, frozen foods, juices or purees contained sulfites above 10?mg?kg^?1. However, all dried apricot samples contained significant levels of sulfite with around 40% having levels exceeding the Turkish limit of 2000?mg?kg^?1. Significant levels of sulfite were found in other samples of dried fruit with even a fruit and nut bar containing 1395?mg?kg^?1 of sulfite, suggesting the dried fruit ingredients contained levels above regulatory limits.     

Inorganic and organic arsenic in some commercial east australian crustacea

The levels of inorganic and organic arsenic have been determined in a total of 86 samples of crustacea which included School prawns (Metapenaeus macleayi), King prawns (Penaeus plebejus), Royal Red prawns (Hymenopenaeus sibogae), Eastern Common crayfish (Jasus verreauxii), Blue Swimmer crab (Portunus pelagicus) and Mud crab (Scylla serrata). Most samples were obtained from New South Wales coastal waters and the remainder were purchased at the Sydney fish markets. Inorganic arsenic was isolated by distillation as the chloride and determined by an atomic absorption-hydride generation method. Organic arsenic was determined on the remaining solution by flame atomic absorption spectrophotometry after digestion of the organic matter with a mixture of nitric, perchloric and sulphuric acids (25 + 5 +1). The Eastern Common crayfish contained the highest levels of inorganic and organic arsenic with ranges of 0.12–0.41 mg kg^?1 and 11.9–54.1 mg kg^?1 (wet basis), respectively. Of the remaining samples, 85% contained inorganic arsenic at <0.1 mg kg^?1 and 97% contained organic arsenic at <7 mg kg^?1. The absolute sensitivity and detection limit of the inorganic arsenic method was estimated to be 3 ng (0.03 mg kg^?1). For the organic arsenic method the sensitivity and detection limits were estimated as 0.5 and 0.8 mg kg^?1, respectively.     

Occurrence of 2,2,4-trimethyl–1,3-pentanediol monoisobutyrate (Texanol®) in foods packed in polystyrene and polypropylene cups

After simultaneous distillation–extraction (SDE) of foods packed in polystyrene (n = 77) and polypropylene cups (n = 42) from 61 different suppliers, coupled capillary gas chromatography–mass spectrometric (HRGC–MS) analyses indicated the presence of diastereomers of 2,2,4-trimethyl–1,3-pentanediol monoisobutyrate (TMPD-MIB; Texanol®), a known coalescent of paints and printing inks. The contaminant was found in 55 and 50% of the polystyrene and polypropylene packed samples, respectively. Amounts ranged 1.2–64.5 µg kg^?1 in polystyrene cups (average 25.1 µg kg^?1) and 0.9–45.7 µg kg^?1 in polypropylene cups (average 10.8 µg kg^?1). The origin of Texanol® in the printed plastic cups was demonstrated by separate HRGC–MS analysis, showing amounts in the higher µg kg^?1 range. In addition, the presence of two pairs of enantiomers, both found to be racemic by enantioselective multi-dimensional gas chromatography–mass spectrometry (enantio-MDGC–MS), excluded it being of natural origin. The detection limit of overall procedure (DLOP) and the reliable quantification limit (RQL) were 0.2 and 0.9 µg kg^?1, respectively. As the diester, 2,2,4-trimethyl–1,3-pentanediol diisobutyrate (TXIB), is on the EU list of regulated substances (restricted to single-use gloves only) with a migration limit of 5 mg kg^?1 in food and is metabolised rapidly by hydrolysis, the observed migration of the monoester Texanol® at the µg kg^?1 level poses no risk of adverse effects.     

A sensitive method for the determination of chlorine-36 in foods using accelerator mass spectrometry

A method using accelerator mass spectrometry (AMS) has been developed to offer a more sensitive alternative to scintillation techniques for the determination of chlorine-36 (³⁶Cl) in foods. The main problem in method development was the potential interference of the sulfur-36 (³⁶S) isobar. This was overcome by reducing the sulfur level of acid digests of food by precipitation of chloride as silver chloride, then purification by washing, dissolution and reprecipitation to present silver chloride as the AMS target. The limit of detection was around 0.1 Bq kg^?1 and the limit of quantitation was around 0.2 Bq kg^?1. The AMS method was only semi-quantitative at the lowest levels of interest. To test the method a few samples of milk (five) and blackberries (three) collected from near two nuclear power stations as potential sources of contamination were analysed. Blackberries spiked at 0.2 Bq kg^?1 and milk spiked at 0.1 Bq kg^?1 could be distinguished from method blanks. There was no ³⁶Cl detectable in the unspiked samples.     

Analysis of environmental chemical residues in products of emerging aquaculture industry in Uganda as case study for Sub-Saharan Africa

A study was conducted to analyse market-regulated heavy metals (lead, mercury and cadmium), organochlorine pesticides and total polychlorinated biphenyls (PCBs) in samples of 38 farmed fish comprising Nile tilapia (Oreochromis niloticus) (20 samples) and African catfish (Clarias gariepinus) (18 samples) from ten selected fish farms in Uganda. The goal of this case study was to understand the safety of aquaculture products from Sub-Saharan Africa. Lead was detected in all the 38 samples (maximum = 1.08 mg kg^?1 (dry weight)), mercury in 31 out of 38 samples (maximum = 0.35 mg kg^?1 (dry weight)), and cadmium in two samples (maximum = 0.03 mg kg^?1 (dry weight)). Total levels of PCBs were below the limit of detection of 0.02 mg kg^?1 (wet weight) in all the samples. Traces of 4,4′-dichloro-diphenyldichloroethylene (DDE) were detected in ten out of 38 samples (maximum = 0.01 mg kg^?1 (wet weight)) making it the most prevalent organochlorine pesticide. Other pesticides detected were: 4,4′-dichloro-diphenyl-trichloroethane (DDT) and endosulfan sulphate, which were found in one fish sample (both 0.002 mg kg^?1 (wet weight)). There was no statistically significant difference between the levels of lead and mercury in catfish and tilapia (t-test at p = 0.05). More catfish samples (eight) contained DDE as compared with tilapia (two). Cadmium, DDT and endosufan sulphate were only detected in catfish implying that catfish is more prone to contamination than tilapia. The levels of contaminants were below the US Food and Drug Administration (USFDA) action levels and European Union maximum residue limits (MRLs), indicating that such fish have the potential for export to these markets.     

Quality of cassava foods in Sierra Leone

Gari and foofoo (fermented cassava foods) were purchased in the Freetown markets of Sierra Leone and analysed for factors associated with quality. Sellers were generally knowledgable about the source of the products which all originated from the country areas outside Freetown. The mean cyanide contents were higher (8.6 mg kg^?1 DM for gari and 28.2 mg kg^?1 DM for foofoo) than the amounts suggested by the Codex specification and, because of the distribution of the values around the mean, some samples necessarily contained unacceptable amounts of cyanide. Cyanogens were present as the cyanohydrin or as free cyanide; no glucoside was detected. Microbiological analysis of the samples showed high counts for total organisms, fungi and Enterobacteriaceae (10⁶–10⁷ g^?1). The mean water content of gari was 119 g kg^?1 which falls within the recommended limit of 120 g kg^?1 but again, due to the distribution of values around the mean, some samples had considerably higher water contents than that limit. Titratable acidity and pH were measured and the mean pH values were 4.18 for foofoo and 4.55 for gari. The particle size and swelling power of gari samples were also measured as these relate to consumer acceptance. The data show the quality of current cassava foods marketed in a major urban centre in Sierra Leone. As centralised processing develops, improvements can be made to those quality parameters which have been identified as important.     

Dietary Intake of Fluoride in the United Kingdom and Fluoride Content of Some Foodstuffs

Using samples from the Total Diet Study, the average dietary intake per person of fluoride in the United Kingdom is estimated to be 1.82 mg day^?1. Beverages account for 71% of the total dietary intake and tea contributes most to the intake from the beverages group. Above-average consumption of tea, as recorded in Great Britain, could result in fluoride intakes as high as 8.9 mg day^?1. It is estimated that tap water containing 1 mg litre^?1 of fluoride could increase normal dietary intakes by 54%. Individual foods have been analysed and the results show that tea infusions and foods containing skin or bone have higher fluoride concentrations than other foods. Concentrations as high as 44 mg kg^?1 were found in the tail meat of krill, and a sample of mechanically deboned meat contained 2.8 mg kg^?1 fluoride. Samples of flour, bread, vegetables, meat and fish products and infant foods generally contained less than 1 mg kg^?1 of fluoride. Soft drinks from an area with a fluoridated water supply had a higher fluoride concentration than samples taken from an area with unfluoridated water.     

Exposure to phthalic acid,phthalate diesters and phthalate monoesters from foodstuffs: UK total diet study results

Phthalates are ubiquitous in the environment and thus exposure to these compounds can occur in various forms. Foods are one source of such exposure. There are only a limited number of studies that describe the levels of phthalates (diesters, monoesters and phthalic acid) in foods and assess the exposure from this source. In this study the levels of selected phthalate diesters, phthalate monoesters and phthalic acid in total diet study (TDS) samples are determined and the resulting exposure estimated. The methodology for the determination of phthalic acid and nine phthalate monoesters (mono-isopropyl phthalate, mono-n-butyl phthalate, mono-isobutyl phthalate, mono-benzyl phthalate, mono-cyclohexyl phthalate, mono-n-pentyl phthalate, mono-(2-ethylhexyl) phthalate, mono-n-octyl phthalate and mono-isononyl phthalate) in foods is described. In this method phthalate monoesters and phthalic acid are extracted from the foodstuffs with a mixture of acidified acetonitrile and dichloromethane. The method uses isotope-labelled phthalic acid and phthalate monoester internal standards and is appropriate for quantitative determination in the concentration range of 5–100 µg kg^–1. The method was validated in-house and its broad applicability demonstrated by the analysis of high-fat, high-carbohydrate and high-protein foodstuffs as well as combinations of all three major food constituents. The methodology used for 15 major phthalate diesters has been reported elsewhere. Phthalic acid was the most prevalent phthalate, being detected in 17 food groups. The highest concentration measured was di-(2-ethylhexyl) phthalate in fish (789 µg kg^–1). Low levels of mono-n-butyl phthalate and mono-(2-ethylhexyl) phthalate were detected in several of the TDS animal-based food groups and the highest concentrations measured corresponded with the most abundant diesters (di-n-butyl phthalate and di-(2-ethylhexyl) phthalate). The UK Committee on Toxicity of Chemicals in Food, Consumer Products and the Environment (COT) considered the levels found and concluded that they did not indicate a risk to human health from dietary exposure alone.     

LC-TOF/MS determination of phthalates in edible salts from food markets in Korea

Residual quantities of 12 phthalates have been monitored in edible salts (raw salts, refined salts, refined salts with additives and baked salts) available in Korean food markets. Liquid–liquid extraction followed by liquid chromatography time-of-flight mass spectrometry (LC-TOF/MS) was used to analyse the samples. The method was validated and showed linear correlation (R ² > 0.996) in the range 0.5–100 ng g^?1 for all target analytes. Recoveries were 85.9–108.4%, except for diethyl phthalate (DEP). Relative standard deviations (RSDs) were 2.7–6.0% and the limits of detection (LODs) were 1.2–2.8 ng g^?1. Although the contamination of phthalates in salt would be trivial in comparison to those of other main foods and below the reference dose of the Chronic Oral Exposure recommended by US-EPA, the availability of reference data could be valuable for food chemists and salt manufacturers.     

Simple determination of formaldehyde in fermented foods by HS‐SPME‐GC/MS

We describe an automatic method to detect formaldehyde (FA) in some fermented foods. This method is based on derivatisation with 2,2,2‐trifluoroethylhydrazine (TFEH) and consecutive headspace solid‐phase micro‐extraction and gas chromatography‐mass spectrometry. FA in food reacted for 30 min at 40 °C with 2,2,2‐TFEH in a headspace vial, and the formed FA‐TFEH derivative was simultaneously vaporised and adsorbed on 85‐μm carboxen–polydimethylsiloxane. Under the established condition, the limit of detection was 0.1 μg kg^?1 by using 1.0‐g solid food and 1.0‐mL liquid food, and the relative standard deviation was less than 10% at FA concentrations between 0.050 and 0.500 mg kg^?1. The concentrations of FA in several traditional Korean foods including gimchi, watery radish gimchi, soybean paste, red pepper paste, soy sauce and bean‐paste soup were measured. All food samples had detectable levels of FA (0.104–13.05 mg kg^?1).     

Ethyl carbamate in fermented foods and beverages: dietary exposure of the Hong Kong population in 2007–2008

To evaluate the potential public health risk of ethyl carbamate (EC), EC exposure from fermented foods and beverages for Hong Kong population was estimated. In 276 samples analysed, EC was detected (limit of detection (LOD) at 0.4?µg?kg^?1) in 202 samples (73%), with higher levels in fermented red bean curd (150–650?µg?kg^?1) and yellow wine (140–390?µg?kg^?1), while low or non-detected (ND) in preserved vegetables (ND–10?µg?kg^?1) and fermented tea (ND–15?µg?kg^?1). The estimated dietary exposure from all fermented foods and beverages was 8.27?ng?kg^?1?bw?day^?1, while exposure excluding alcoholic beverages was 5.42?ng?kg^?1?bw?day^?1, with calculated margins of exposure (MOEs) at 3.6?×?10⁴ and 5.5?×?10⁴ respectively. The risk of adverse health effects was low for the average population but higher (MOE?of?10³) for high consumers of alcoholic beverages especially habitual drinkers of alcoholic types with high EC contents.     

Determination of plasticisers and BPA in Sicilian and Calabrian nectar honeys by selected ion monitoring GC/MS

Twenty-six plasticisers and bisphenol A (BPA) in 39 Sicilian and Calabrian nectar honeys of different botanical south Italian origin were determined by GC-MS. Di-(2-ethylhexyl)phthalate was the most abundant plasticiser in all samples, reaching up 202.7 ± 153.1 µg kg^–1, followed by di-butylphthalate with a concentration of 40.3 ± 9.3 µg kg^–1, whereas the concentration of the other phthalates varied from not detectable to 68.2 µg kg^–1. Trace levels of adipate, sebacate and BPA were not detected in any samples. Among the different floral origin honeys, di-ethylphthalate levels were above the limit of quantification (LOQ) in orange blossom, wildflower and chestnut honey samples. Among the honeys of different geographical origin, di-methylphthalate, di-butylphthalate and di-(2-ethylhexyl)phthalate concentrations were similar. Calabrian honeys showed levels of di-ethylphthalate always lower than the LOQ, moreover di-(2-methylpropyl)phthalate levels were lower than the Sicilian ones. On the contrary, in Sicilian honeys di-(2-methylpropyl)phthalate levels were higher and di-ethylphthalate was present in 37% of samples.     

Survey and risk assessment of trace elements in foods from Taiwan containing red mould rice (Monascus) by ICP-MS

The concentrations of seven trace elements (As, Cd, Cr, Pb, Se, Cu and Zn) in 93 red mould rice (Monascus) food samples in Taipei, Taiwan, were determined by inductively coupled plasma-mass spectrometry (ICP-MS) after wet digestion. The results, calculated in mg?kg^?1 (wet weight) for each sample, revealed the general scenario of food safety in Taiwan: As (0.005–12.04), Cd (<0.0005–2.22), Cr (0.014–6.95), Cu (0.012–8.70), Pb (0.001–0.64), Se (<0.001–1.29) and Zn (0.020–67.02). Three food samples were identified with As concentrations higher than regulatory limits: a dietary supplement sample and a seaweed sample with As concentrations that exceeded the limit of Taiwan's health food standard of 2?mg?kg^?1, and a canned eel sample with an As concentration that exceeded the limit of Canada's fish standard of 3.5?mg?kg^?1. This study suggests that the estimated intakes of these seven trace elements from the consumption of foods containing Monascus pose little risk, as the trace element contents in the majority of samples were lower than the permissible/tolerable intakes per week according to the guidelines recommended by the Food and Agricultural Organization/World Health Organization (FAO/WHO). Moreover, their concentrations in foods containing Monascus differ widely for different food varieties, suggesting that external contaminants and raw materials are the main sources of trace elements. This study shows that ICP-MS is a simple method proposed for the determination of As, Cd, Cr, Pb, Se, Cu, and Zn in foods containing Monascus.