Furan in commercial baby foods from the Spanish market: estimation of daily intake and risk assessment

ABSTRACT

The occurrence of furan in commercial baby food samples from the Spanish market was evaluated using an automated headspace solid-phase microextraction method coupled to gas chromatography-mass spectrometry (HS-SPME-GC-MS). A total of 76 baby food samples including infant formula, baby cereals, fruit in cans and/or jars, vegetables, meat, and fish, were surveyed for furan content. The lowest concentration of this compound was found in infant formula (<0.02–0.33 ng ml^?1), and cereal-based food (0.15–2.1 ng g^?1) while baby food containing fish showed the highest concentrations (19–84 ng g^?1). Following recommendation of the European Food Safety Authority (EFSA), the effect on furan content was evaluated of consumer home preparation of foods, heating and handling. Furan concentrations were reduced by up to 35% when samples were heated in a dish using microwave oven and by up to 53% when a hot water bath was used. Finally, we estimated the furan intake from baby food consumption (0.002–1.18 µg kg^?1 body weight day^?1) and we calculated the margin of exposure (MOE) from samples as purchased and also after home preparation of the food. For infant formula and cereal baby foods, the MOEs (26,278–412,776) indicated no infant health concern or priority, while for meat and fish-based baby foods the values pointed to a potential public health risk, even considering the furan losses during preparation at home.     

Compositional variation in β‐carotene content,carbohydrate and antioxidant enzymes in selected banana cultivars

Banana is one of the most important tropical fruits, and India ranks first in its world production. Banana cultivars rich in provitamin A carotenoids may offer a potential food source for alleviating vitamin A deficiency, particularly in developing countries. With a view to exploit banana peels as a source of valuable components, in the present study, proximate composition, carotenoids, beta‐carotene and some anti‐oxidative enzymes as well as carbohydrate content of selected Indian banana varieties were determined. Karpooravalli cultivar of banana showed the maximum accumulation of carotenoid content in the non‐edible (68 μg g^?1 d.w.) portion of banana, while being the second highest in beta‐carotene content (143.12 μg per 100 g). However, Red Banana ranked highest in total carotenoid contents for pulp (4 μg g^?1 d.w.) and beta‐carotene was estimated to be the highest in the case of peels (241.91 μg per 100 g) and in pulp (117.2 μg per 100 g). Karpooravalli cultivar of banana is also rich in carbohydrate content in terms of total starch (1786.0 μg g^?1 d.w. in peels and 544.85 μg g^?1 d.w. in pulp) and sugars (53.53 μg g^?1 d.w. in peels and 39.05 μg g^?1 d.w. in pulp). The catalase enzyme activity in these peels ranged from 5.66 to 35.57 nmol min^?1 mg^?1 proteins and was found at a higher level in cultivar Poovan, while the ascorbate peroxidase showed the range of 2.25 to 6.22 μmol min^?1 mg^?1 proteins. The peels of cultivars Red Banana and Karpooravalli are rich source of bioactive compounds, such as carotenoids (beta‐carotene), anti‐oxidative enzymes and carbohydrate contents.     

Analysis of perchlorate in baby food on Canadian (Ottawa) markets in 2009 and estimated dietary exposure

ABSTRACT

In order to determine the baseline levels of perchlorate in major brands of baby food, 200 baby food products were collected from retail stores in Ottawa, Canada and analysed for perchlorate in 2010. The seven food groups tested were fruit, juices, vegetables, meat, yogurt, mixed (vegetable mixed with meat) and other (e.g. vegetable mixed with meat and cereal, cheese, egg,). Samples were extracted with a mixture of methanol and 1% acetic acid (4:1, v/v). Determination was conducted by stable isotope dilution ion chromatography tandem mass spectrometry (ID-IC-MS/MS). The complexity of different food matrices required additional method validation. The perchlorate levels in 46 samples were found to be lower than the quantification limit (0.2 ng g^?1). The perchlorate levels in the other 154 baby food samples were also low; about 96.7% of the baby foods had perchlorate levels less than 10 ng g^?1 (ranged from 0.2 to 22.4 ng g^?1, median1.35 ng g^?1); only 5 samples had perchlorate levels higher than 10 ng g^?1. Dietary exposure to perchlorate from analysed baby food was conservatively estimated to range from 0.007 to 0.121 µg/kg bw/d based on the mean intake for children (1–5 years old).     

Headspace Liquid-Phase Microextraction Followed by Gas Chromatography–Mass Spectrometry for Determination of Furanic Compounds in Baby Foods and Method Optimization Using Response Surface Methodology

In the present study, a sensitive, rapid, and simple method for determination of furanic compounds in baby foods has been developed. Headspace liquid-phase microextraction (HS-LPME) coupled with gas chromatography–mass spectrometry was used to extract and measure furan, 2-methylfuran, and 2,5-dimethylfuran in baby foods. Effective parameters such as salt amount (NaCl), stirring rate, temperature, and time of extraction were optimized using response surface methodology based on a central composite design to obtain the best conditions for extracting furanic compounds. The optimum parameter values were 1 g NaCl, 700 rpm stirring rate, 40 °C extraction temperature, and 15 min extraction time. The calibration curves were linear over the range of 0.2–200 ng?mL^?1 (R ² ?>?0.99) for all compounds, and the repeatability of the method, described as relative standard deviation, ranged between 3.84 and 7.06 % (n?=?6). The recovery of spiked baby food sample after extraction ranged between 89.33 and 103.64 %, and the best enrichment factor was achieved about 972-fold for furan. The limits of detection and quantitation ranged between 0.021 and 0.038 ng?g^?1 and 0.069 and 0.126 ng?g^?1, respectively. The merit figures of the HS-LPME/GC-MS method showed that it can be considered as a new, fast, and effective alternative method for investigating furanic compounds in baby foods.     

Exposure assessment to ochratoxin A in Catalonia (Spain) based on the consumption of cereals,nuts, coffee,wine, and beer

Ochratoxin A (OTA) was analysed in composite samples of cereal-based baby foods, beer, breakfast cereals (corn- and rice and wheat-based), loaf bread, peanuts and pistachios. Foodstuffs were collected in hypermarkets and supermarkets from 12 cities in the Spanish region of Catalonia, and composite samples were prepared for analysis involving liquid–liquid extraction, followed by immunoaffinity column clean-up and HPLC with fluorescence detection. Consumption data for the selected foodstuffs were collected by means of a food-frequency questionnaire. The studied population was grouped by age in infants, children, adolescents and adults; and exposure to OTA through the specified foodstuffs, and through wine and coffee, was assessed. Exposure assessment was done through deterministic and probabilistic modelling of the contamination and consumption data. OTA occurrence and mean of positive samples (ng?g^?1 or ng?ml^?1, for beer) were the following: 8.7% and 0.233 in baby foods; 88.7% and 0.022 in beer; 2.8% and 0.728 in corn-based breakfast cereals; 25% and 0.293 in wheat-based breakfast cereals; 12.9% and 0.283 in loaf bread; 41.7% and 0.241 in peanuts; and 2.9% and 0.228 in pistachios. The median estimated daily intake of OTA through the foodstuffs by each age group were below the latest provisional tolerable daily intakes (PTDIs) of 17 and 14?ng?kg^?1?bw?day^?1 recommended by the European Food Safety Authority (EFSA) in 2006 and the Joint FAO/WHO Expert Committee on Food Additives (JECFA) in 2007, respectively, ranging from 1% and 2% of those values in adolescents and children, to 3% and 11% in adults and infants.     

The proximate composition and some minor constituents of poppy seeds

The proximate chemical composition of poppy seeds, along with minerals and water-soluble vitamins content was investigated. The compositions of the fatty acids and tocopherols of the extracted oil were also determined. The proximate analysis of poppy seeds showed the following composition: (440 g kg^?1), protein (211 g kg^?1), moisture (50 g kg^?1), ash (63 g kg^?1), crude fine (62 g kg^?1) and total carbohydrates (236 g kg^?1). Potassium and calcium were the predominant elements in the poppy seeds. Linoleic acid was the major unsaturated fatty acid (750 g kg^?1 total fatty acids) while palmitic acid was the main saturated one (86-4 g kg^?1). The amounts of α-, β- and δ-tocopherols found in poppy seed oil were 220 μg g^?1, 40 μg g^?1 and 20 μg g^?1 respectively. Among the water-soluble vitamins determined, pantothenic acid was found at the highest level followed by niacin and thiamin.     

The effects of sex and seasonality on the metal levels of different muscle tissues of mature Atlantic blue crabs (Callinectes sapidus) in Mersin Bay,north‐eastern mediterranean

The objective of this study was to determine the seasonal and sexual effects on metal levels of lump crabmeat (LCM) and chela crabmeat (CCM) of mature Atlantic blue crabs, Callinectes sapidus, caught in the Mersin Bay, the north‐eastern Mediterranean. The findings indicated that the annual ranges of metal levels in the LCM of Atlantic blue crab were as follows: 0.44–0.61 μg Cd g^?1, 0.30–0.60 μg Cr g^?1, 0.24–0.52 μg Pb g^?1, 9.72–43.70 μg Cu g^?1, 39.52–97.26 μg Zn g^?1, 11.97–32.48 μg Fe g^?1. The annual range of metal levels in the CCM of Atlantic blue crab were as follows: 0.52–1.07 μg Cd g^?1, 0.24–0.61 μg Cr g^?1, 0.28–0.56 μg Pb g^?1, 22.17–68.09 μg Cu g^?1, 93.92–175.21 μg Zn g^?1, 8.81–19.47 μg Fe g^?1. Cd, Cu, Zn levels in CCM of Atlantic blue crabs were higher than in LCM, whereas Fe levels were found lower (P < 0.05). Fe metal specifically accumulated in LCM, and Cd, Cu and Zn metals accumulated in CCM. Metals such as Cu, Zn and Fe showed seasonal variations. It was found out that Cu, Zn and Fe levels of muscle tissues of the Atlantic blue crab in spring and summer seasons were higher than in autumn and winter seasons.     

Assessment of PCDD/F,PCB, OCP and BPA dietary exposure of non-breast-fed European infants

The aim of this study is to obtain data on the exposure of non-breast-fed infants to polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F), polychlorinated biphenyls (PCB), organochlorine pesticides (OCP), and bisphenol A (BPA) and its chlorinated derivatives through consumption of commercial infant foods with largest shares of the market in 22 European Union countries. The E-Screen bioassay was employed to assess the oestrogenicity of the baby foods and the ethoxyresorufin-O-deethylase (EROD) induction was measured to determine the levels of PCDD/F and PCB. Consequently, the highest total effective xenoestrogen burden (TEXB) of 73.60?pM?Eeq?g^?1 was found in the soy-based formula and the EROD bioassay was always below the limit of quantification (LOQ) (3.5?pg?g^?1). Overall, the estimated dietary exposure to BPA via commercial baby foods was lower than the tolerable daily intake (TDI) of 50?µg?kg^?1 body weight (bw). Furthermore, the findings indicated that the dietary exposure of 0–9-month-old infants through the products investigated here does not exceed the maximum TDI of 4?pg WHO-TEQ (toxic equivalents)?kg^?1 bw. However, exposure to more than 2?pg WHO-TEQ?kg^?1?bw?day^?1 might occur for 0–4-month-old infants consuming ‘starting’ hypoallergenic formula. Moreover, analysis of OCP indicated that the dietary exposure of non-breast-fed infants was not harmful. Considering the importance of early development and the vulnerability of infants and children, it is essential to determine their dietary exposure to contaminants in order to decide which efforts of risk reduction should receive highest priority.     

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.     

Simultaneous determination of vitamins A and E in feeds and foods by reversed phase high-pressure liquid chromatography

A simple high-pressure liquid chromatographic method for the simultaneous determination of vitamins A and E in animal feeds and foods has been developed and evaluated. After saponification and extraction the sample was run on a reversed-phase column with water-methanol as the mobile phase. The detector was an u.v.-lamp at 280 nm. The method has been tested on different types of feeds and foods containing between 2-30 μg vitamin A g^?1 of sample and 5-300 μg vitamin E g^?1 of sample. The recovery of added vitamins was 86 % for retinylacetate and 91 % for α-tocopheryl-acetate with a standard deviation of 3 % for both. Results of the proposed procedure agreed well with those obtained by other methods.     

Cadmium and lead content in fresh and canned peas

Cadium and lead in raw, blanched and canned peas were determined using atomic absorption spectrophotometry. The daily intake of cadmium and lead from peas in Spain was evaluated. The cadmium content of the peas ranged from less than 0.004 to 0.015 μg^?1, whereas the lead content varied from 0.49 to 0.223 μg^?1. The concentraiton of both elements was compared at different stages of the process. Statistically significant differences were found in the lead levels as a function of size and the different stages of the canning process. The mena level of cadmium and lead (0.041 μgg^?1 and 0.092 μgg^?1 respectively) could account for a daily intake of 0.1 μg day^?1 for cadmium and 1.1 μg day^?1 for lead.     

Development of an analytical method and survey of foods for furan, 2-methylfuran and 3-methylfuran with estimated exposure

Furan has been found to form in foods during thermal processing. These findings, a classification of furan as a possibly carcinogenic to humans, and a limited amount of data on the concentration of furan in products on the Canadian market prompted the authors to conduct a survey of canned and jarred food products. Methyl analogues of furan, 2-methylfuran and 3-methylfuran, were analysed concurrently with furan via a newly developed isotope dilution method, as these analogues were detected in foods in the authors’ earlier work and are likely to undergo a similar metabolic fate as furan itself. The paper reports data on 176 samples, including 17 samples of baby food. The vast majority of samples were packaged in cans or jars. Furan was detected above 1 ng g^?1 in all non-baby food samples with a median of 28 ng g^?1 and concentrations ranging from 1.1 to 1230 ng g^?1. Also, 96% of these samples were found to contain 2-methylfuran above 1 ng g^?1 with a median of 12.8 ng g^?1 and a maximum concentration of 152 ng g^?1, while 81% of samples were found to contain 3-methylfuran above 1 ng g^?1 with a median of 6 ng g^?1 and a maximum concentration of 151 ng g^?1. Similarly, furan was detected above 1 ng g^?1 in all baby food samples with a median of 66.2 ng g^?1 and concentrations ranging from 8.5 to 331 ng g^?1. Also, 100% of these samples were found to contain 2-methylfuran above 1 ng g^?1 with a median of 8.7 ng g^?1 and a maximum concentration of 50.2 ng g^?1, while 65% of samples were found to contain 3-methylfuran above 1 ng g^?1 with a median of 1.6 ng g^?1 and a maximum concentration of 22.9 ng g^?1. Additionally, three coffee samples were analysed ‘as is’, without brewing, and were found to have high levels of furans, especially 2-methylfuran, at a maximum of 8680 ng g^?1. Using this data set, dietary exposures to furan and total furans were calculated. Average furan and total furan intakes by adults (≥20 years) were estimated at approximately 0.37 and 0.71 µg kg^?1 of body weight day^?1 respectively.     

A survey of styrene monomer levels in foods and plastic packaging by coupled mass spectrometry—automatic headspace gas chromatography

An extensive UK survey of styrene monomer levels in styrene based plastic packaging materials and their contained foods (133 samples) has been carried out, examining a wide range of retail foods of different brand names and including yogurts, creams, salads, coleslaws, soft cheeses, margarines, hot and cold beverages from dispensing machines, spreads, fresh and cooked meats, candied fruits, fresh strawberries, and take-away ‘fast’ foods. Analysis by headspace gas chromatography of styrene levels in the plastic containers showed levels of monomer ranging from 16 to 1300 mg kg^?1 although the majority of containers (73%) had styrene levels in the range 100–500 mg kg^?1 and only five plastic tubs had levels exceeding 1000 mg kg^?1. Analysis of the food contents of the plastic containers by automated headspace gas chromatography with single ion monitoring mass spectrometric detection showed levels of the monomer ranging from < 1 μg kg^?1 to 200 μg kg^?1, although the majority of foods (77%) had styrene levels below 10 μg kg^?1, and 26% of the total number analysed had levels below 1 μg kg^?1.     

Are Chileans exposed to dietary furan?

Chilean consumer preferences include foods that may contain considerable amounts of furan, a potential human carcinogen. However, there is no information regarding dietary exposure to furan in Chile. Thus, the objective of this work was to determine the Chilean exposure to dietary furan. To accomplish this objective, the furan concentration of 14 types of commercial foods processed at high temperature were analysed based on a modified headspace-GC/MS (HS-GC/MS) method in which the limits of detection for different food matrices ranged from 0.01 to 0.6 ng g^?1. In addition, a risk assessment was made with exposure estimates based on dietary data from national studies on different age groups (9-month-old babies, school children, adults and elderly people). Of the food items surveyed “American”-type coffee (espresso coffee plus hot water) obtained from automatic coffee machine (936 ng g^?1) and low moisture starchy products like crisps and “soda”-type crackers showed the highest furan concentrations (259 and 91 ng g^?1, respectively). Furthermore, furan was also found in samples of breakfast cereals (approximately 20 ng g^?1), jarred fruit baby foods (8.5 ng g^?1) and orange juice (7.0 ng g^?1). School children (aged 9–13 years) represented the highest intake of furan (about 500 ng kg^?1_bw day^?1), with margins of exposure of 2479 and 2411, respectively, which points to a possible public health risk.     

Sorption of sulphate and distribution of total,sulphate and mineralisable sulphur in some tropical soil profiles in tanzania

The forest soils from Arusha generally contained more total S (129–439, average 277 μg S g^?1) throughout the profile than the cultivated ones from Mbeya (32–408, average 143 μg S g^?1). Total S in the surface horizons was in the range of 120–439, average 292 μg S g^?1. The contents of total and organic S in the profiles were significantly (P <0.001) correlated with the contents of organic C and total N. Although both extractants—0.5M-NH₄OAC and 0.01M-CaCl₂—yielded nearly similar results, the latter tended to extract a little more sulphate than the former from organic matter rich soils. Sulphate distribution in a profile was related to sorption capacities of the soils from various horizons. Its content in the profiles was in the range of 1–34, average 15 μg S g^?1, and was significantly (P <0.05) but negatively correlated with the ratios of C:N and C:S. Maximum S mineralisation occurred in the surface soil of most of the profiles. Less mineralisation or marked immobilisation took place in the subsurface soil. Mineralisation-immobilisation relationship was mainly affected by C: S ratio of the soil. A soil C: S ratio of 200:1 was found to be critical below which net mineralisation and above which immobilisation took place.     

Utility of 4-chloro-7-nitrobenzofurazan for the spectrofluorimetric determination of butylated hydroxyanisole and propyl gallate in foodstuffs

Abstract: A spectrofluorimetric method is presented for the determination of 2 synthetic phenolic antioxidants (SPAs), butylated hydroxyanisole (BHA), and propyl gallate (PG) in foodstuffs. The proposed method is based on the derivatization of SPAs with 4‐chloro‐7‐nitrobenzofurazan (NBD‐Cl) in phosphate buffer of pH 9.0 to yield a highly fluorescent brown product. The optimum experimental conditions have been studied carefully. Linear calibration curves were obtained over the concentration range of 0.20 to 40 μg mL^?1 for BHA, and 0.80 to 50 μg mL^?1 for PG, using NBD‐Cl reagent. The detection limits were 18 ng mL^?1 for BHA, 55 ng mL^?1 for PG. Intra‐day and inter‐day relative standard deviations at 3 different concentrations were determined. The high recovery values indicate the accuracy of the proposed methods, and low relative standard deviation values indicate good precision. The results presented in this report show that the applied spectrofluorimetric method is acceptable for the determination of the 2 SPAs in the foodstuffs. Other SPAs, tertiary butyl hydroquinone and butylated hydroxytoluene in foodstuffs do not interfere with the proposed method. Practical Applications: In this spectrofluorimetric method, NBD‐Cl as a derivation agent is used to detect synthetic phenolic antioxidants. The method specificity has been greatly improved; there was no interference from other commonly used phenolic substances.     

Comparison of four analytical techniques based on atomic spectrometry for the determination of total tin in canned foodstuffs

Different techniques for the determination of total tin in beverages and canned foods by atomic spectrometry were compared. The performance characteristics of inductively coupled plasma-mass spectrometry (ICP-MS), hydride generation-inductively coupled plasma-atomic emission spectrometry (HG-ICP-AES), electrothermal atomisation-atomic absorption spectrometry (ETA-AAS) and inductively coupled plasma-atomic emission spectrometry (ICP-AES) were determined in terms of linearity, precision, recovery, limit of detection, decision limit (CCα) and detection capability (CCβ) (Decision 2002/657/EC). Calibration ranges were covered from ng?l^?1 to mg?l^?1 level. Limits of detection that ranged from 0.01, 0.05, 2.0 to 200?µg?l^?1 were reached for ICP-MS; HG-ICP-AES; ETA-AAS and ICP-AES, respectively. Precision, calculated according to ISO 5725-2 for repeatability and within-laboratory reproducibility and expressed as relative standard deviation (RSD), ranged from 1.6% to 4.9%; and recovery, based on Decision 2002/657/EC, was found to be between 95% and 110%. Procedures for the mineralisation or extraction of total tin were compared. Wet digestion, sequentially, with nitric acid and hydrogen peroxide provided the best results. The influence of possible interferences present in canned food and beverage was studied, but no interference in the determination of tin was observed. Since maximum levels for tin established by European Union legislation vary from 50?mg?kg^?1 in canned baby foods and infant foods up to 200?mg?kg^?1 in canned food, ICP-AES was chosen as the preferred technique for routine analysis thanks to its good precision, reliability and ease of use. The accuracy of this routine method was confirmed by participation in six proficiency test schemes with z-scores ranging from ?1.9 to 0.6. Several canned foodstuffs and beverage samples from a local market were analysed with this technique.     

Inexpensive,rapid screening method for aflatoxins in peanuts and peanut products

Surveys of major Brazilian foodstuffs demonstrated that peanuts and peanut products continue to be very susceptible to aflatoxin contamination. To prevent, or at least minimise, the problem the aflatoxins need to be monitored by a rapid and inexpensive screening method. The AOAC Romer method has been used and found highly reliable. However, the clean-up step utilises anhydrous FeCl₃ and basic CuCO₃ which are expensive and not readily available in Brazil. Thus, the extraction (with a mixture of 270 ml methanol plus 30ml 40 g litre^?1 aqueous KCl) and clean-up (150 ml 100 g litre^?1 aqueous CuSO₄) steps of the method of Soares and Rodriguez-Amaya (1985) were combined with the AOAC minicolumn to provide a rapid, inexpensive screening technique. Fifty-two sample lots of peanuts and peanut products were screened by this and Romer's method, and the results were in complete agreement: 28 samples were negative, four < 20 μg kg^?1, 12 in the range 20–50 μg kg^?1, three in the range 50–100 μg kg^?1 and 5 >100 μg kg^?1. The results also agreed well when the extracts obtained by the two methods were submitted to quantitative TLC.     

Migration of bisphenol A from plastic baby bottles,baby bottle liners and reusable polycarbonate drinking bottles

Human exposure to bisphenol A (BPA) has recently received special attention. It has been shown that exposure to BPA may occur through the consumption of beverages or foods that have been in contact with polycarbonate (PC) plastic containers or epoxy resins in food packaging. A BPA migration study was conducted using a variety of plastic containers, including polycarbonate baby bottles, non-PC baby bottles, baby bottle liners, and reusable PC drinking bottles. Water was used to simulate migration into aqueous and acidic foods; 10% ethanol solution to simulate migration to low- and high-alcoholic foods; and 50% ethanol solution to simulate migration to fatty foods. By combining solid-phase extraction, BPA derivatization and analysis by GC-EI/MS/MS, a very low detection limit at the ng l^?1 level was obtained. Migration of BPA at 40°C ranged from 0.11 µg l^?1 in water incubated for 8 h to 2.39 µg l^?1 in 50% ethanol incubated for 240 h. Residual BPA leaching from PC bottles increased with temperature and incubation time. In comparison with the migration observed from PC bottles, non-PC baby bottles and baby bottle liners showed only trace levels of BPA. Tests for leachable lead and cadmium were also conducted on glass baby bottles since these represent a potential alternative to plastic bottles. No detectable lead or cadmium was found to leach from the glass. This study indicated that non-PC plastic baby bottles, baby bottle liners and glass baby bottles might be good alternatives for polycarbonate bottles.