Determination of aflatoxin M1 level in milk in the production of baby and children's food using immunoassay]

Using commercial immunokits the concentration of aflatoxin M1 was measured in 376 samples of raw milk from farms in the area of a new dairy plant producing milk baby foods. 87.8% of the samples contained no aflatoxin M1 (detection limit 0.025 micrograms/l) and only 2 samples (0.5%) possessed higher concentration than 0.1 microgram/l, which represents the tolerance limit for aflatoxin M1 in baby milk foods admitted in Czechoslovakia.     

Occurrence of aflatoxins in peanuts, milk, and animal feed in Trinidad

The prevalence of aflatoxin B1 (AFB1) in 186 peanut products (140 peanuts, 32 peanut butter, and 14 nut cakes) from supermarkets, road vendors, and sale outlets, and 40 feed samples from dairy farmers was determined using the radioimmunoassay method (Charm II) test for aflatoxins. The frequency of aflatoxin M1 (AFM1) was also determined in 175 raw milk samples from milk collection centers and 37 pasteurized milk samples obtained from supermarkets and sale outlets. Overall, from a total of 438 samples tested, 18 (4.1%) were positive for aflatoxin comprising 5 (2.2%) of 226 peanut products and feeds positive for AFB1, and 13 (6.1%) of 212 milk samples positive for AFM1. All 186 peanuts and peanut products were negative (0.0%) for AFB1 while 5 (7.4%) of 40 dairy feed samples were positive. Of the 175 raw milk samples tested, 13 (7.4%) were contaminated with AFM1 while all pasteurized milk samples were negative. The detection of AFB1 in feed and AFM1 in milk is of public health importance considering the practice of raw milk consumption by the farmers and their families in the country.     

Microbiological quality of raw goat's and ewe's bulk-tank milk in Switzerland

A total of 407 samples of bulk-tank milk (344 of goat's milk and 63 of ewe's milk) collected from 403 different farms throughout Switzerland, was examined. The number of farms investigated in this study represents 8% of the country's dairy-goat and 15% of its dairy-sheep farms. Standard plate counts and Enterobacteriaceae counts were performed on each sample. Furthermore, the prevalence of Staphylococcus aureus, Campylobacter spp., Shiga toxin-producing Escherichia coli, Salmonella spp., and Mycobacterium avium ssp. paratuberculosis was studied. The median standard plate count for bulk-tank milk from small ruminants was 4.70 log cfu/ml (4.69 log cfu/ml for goat's milk and 4.78 log cfu/ml for ewe's milk), with a minimum of 2.00 log cfu/ml and a maximum of 8.64 log cfu/ml. Enterobacteriaceae were detected in 212 (61.6%) goat's milk and 45 (71.4%) ewe's milk samples, whereas S. aureus was detected in 109 (31.7%) samples of goat's milk and 21 (33.3%) samples of ewe's milk. Campylobacter spp. and Salmonella spp. were not isolated from any of the samples. However, 16.3% of the goat's milk and 12.7% of the ewe's milk samples were polymerase chain reaction (PCR)-positive for Shiga toxin-producing E. coli. Seventy-nine (23.0%) goat's tank-milk and 15 (23.8%) ewe's tank-milk samples were PCR-positive for insertion sequence 900, providing presumptive evidence for the presence of M. avium ssp. paratuberculosis. These results form the basis for determining the microbiological quality standards for goat's and ewe's milk. Moreover, the data presented form part of the risk assessment program for raw milk from small ruminants in Switzerland.     

Monitoring of warmed-over flavour in pork using the electronic nose - correlation to sensory attributes and secondary lipid oxidation products

Sensory analysis of meatballs was carried out to monitor the warmed-over flavour (WOF) development in cooked, cold-stored (at 4 °C for 0, 2 and 4 days) and reheated meatballs derived from M. longissimus dorsi (LD) and M. semimembranosus (SM) of pigs fed a standard diet supplemented with either 3% of rapeseed oil or 3% of palm oil. This was performed in combination with measurement of volatile compounds using a solid-state-based gas sensor array system (electronic nose) and gas chromatography/mass spectrometry together with measurement of thiobarbitoric acid reactive substances (TBARS). Subsequently, to elucidate the relations and predictability between the obtained data, the gas sensor responses were correlated with chemical (volatile and non-volatile secondary lipid oxidation products) and sensory data (flavour and odour attributes), using partial least squares regression modelling (PLSR). The TBARS, hexanal, pentanal, pentanol and nonanal all correlated to the sensory attributes associated to WOF formation. Moreover, the responses from eight of the MOS (metal oxide semiconductor) sensors within the electronic nose proved to be significantly related to WOF characteristics detected by both sensory and chemical analysis, while six of the MOSFET (metal oxide semiconductor field effect transistor) sensors were related to freshly cooked meat attributes determined by sensory analysis. The obtained results show the potential of the present gas sensor technology to monitor WOF formation in pork.     

Aflatoxin M<Subscript>1</Subscript> in pasteurized and raw milk from organic and conventional systems

Aflatoxin M₁ is one of the most common toxic natural substances found worldwide. It metabolizes from aflatoxin B₁ that is present in the diet of mammals. In this study, 84 milk samples were investigated in total, and 63 (75 %) were contaminated with aflatoxin M₁ above the limit of detection. No difference was observed between the samples from organic and conventional systems (0.021 vs. 0.018 µg/kg; p > 0.05). There was no difference between pasteurized and raw milk samples (0.018 vs. 0.020 µg/kg; p > 0.05). None of the samples contained aflatoxin M1 above the maximum level permitted by Brazilian Legislation (0.5 µg/kg for fluid milk). The estimated daily intake (EDI) of aflatoxin M₁ through organic and conventional milk consumption was also evaluated. In this study, the EDI-values for aflatoxin M₁ did not pose a toxicological risk for the population. To our best knowledge, this is the first report on aflatoxin M₁ levels in organic milk from Brazil.     

Use of ultraviolet energy to degrade aflatoxin M1 in raw or heated milk with and without added peroxide

Raw whole milk was artificially contaminated to contain 1 ppb aflatoxin M1. A thin layer of milk (.1 cm) was irradiated with ultraviolet energy. In the first experiment, milk was held at 90 degrees C for 10 min, cooled to 20 degrees C, and irradiated for 30 min. Amount of aflatoxin M1 decreased equally (56.2 vs. 53.9%) in raw or preheated milk, suggesting no involvement of milk enzymes in degrading aflatoxin M1 by ultraviolet energy. Data obtained when raw milk containing aflatoxin M1 was exposed to ultraviolet energy for 15 to 60 min suggest first order kinetics for the degradation reaction. In another experiment, milk was held at 5, 25, or 65 degrees C while it was being irradiated. Aflatoxin M1 was degraded at all temperatures. Amount of toxin decreased nonlinearly when temperature at which milk was held was increased. Presence in milk of benzoyl peroxide at .002% did not change the extent to which aflatoxin M1 was degraded by irradiation. Amount of toxin, however, decreased by 89.1% in milk containing .05% H2O2 as compared with 60.7% for H2O2-free milk when both were exposed to ultraviolet irradiation for 20 min at 25 degrees C.     

Measurement of odour after in vitro or in vivo ingestion of raw or heated garlic, using electronic nose, gas chromatography and sensory analysis

The possibility of characterising the garlic odour in in vitro and in vivo was demonstrated using the newly developed electronic nose, based on an array of metal oxide semiconductor sensors. Two grams of raw and heat‐treated garlic, and breath odour after eating 2 g of raw garlic and heat‐treated garlic were analysed with an electronic nose. Furthermore, calculation of F‐value (odour quality) and S‐value (odour strength) demonstrated distinct odour differences between the samples, and that the electronic nose could differentiate between the various garlic associated odours corresponding to the different origins (in vivo or in vitro), or to the different processing (raw or heat‐treated). The correlation between gas chromatography and sensory analysis was also discussed in order to identify the volatile compounds in the sample, and to investigate the association with the response of human perception to the samples. Results showed that odour sensor data were easier to obtain and were well correlated with both types of instrument.     

Evaluation of spectrophotometric and fluorometric methods for alkaline phosphatase activity determination in ewe's milk

The alkaline phosphatase (ALP) activity test has been used since 1935 to assess the effectiveness of pasteurization. Different analytical methods exist for detecting ALP in milk. Unfortunately, there is little information about ALP activity in ewe's milk. The aim of this study was to assess and compare the official European method (spectrophotometric method) and the Fluorophos method (fluorometric method) regarding their use in ewe's milk. Bulk ewe's milk samples were taken from a flock and from three different dairies. A portion of the original sample was pasteurized at 63 degrees C for 30 min in a circulating bath; another portion was heated to and kept at 95 degrees C for about 2 min, and 0.1% (vol/vol) of raw milk was added. The samples obtained were analyzed in duplicate using the spectrophotometric and fluorometric methods. The relation between ALP activity determined by the two methods was characterized by the following equation: Y = 1.34 + 0.0039X (where Y = ALP in microg of phenol per ml of milk and X = ALP in mU/liter; R2 = 91.5%). Precision parameters (repeatability [r], standard deviation of repeatability [s(r)], and relative standard deviation of repeatability [RSDr]) for both methods were calculated. The values of RSDr for the Fluorophos method were 4.30 for pasteurized milk and 2.96 for 0.1% raw milk, close to the value indicated by Rocco in whole cow's milk (RSDr = 4.4). The repeatability for the official method (r = 2.16) was close to that indicated for whole cow's milk (r = 2).     

A STUDY ON THE OCCURRENCE OF AFLATOXIN IN RAW MILK DUE TO FEEDS

Milk and milk products are the most important group of food which carries aflatoxin to the people. Therefore, the existence of aflatoxin M₁ (AFM₁) in milk is a potential risk for public health. AFM₁ existence in milk and milk products was found in studies performed in Turkey. In this study, aflatoxin contamination was detected in 48 raw milk and 48 feed samples. Milk and feed samples, in which the positive sample rate was determined as 24%, included different levels of aflatoxin. Altogether, 20 raw milk samples (41.67%) and 15 feed samples (31.25%) contained over the level of legal limits established by the Turkish Food Codex (TFC) and the European Communities (EC) regulation in positive samples. According to these results, the milk and feed samples collected from this area constitute a potential risk for public health. The most effective way of controlling aflatoxin M₁ in milk is to reduce the contamination of aflatoxin in raw milk and feed samples. Both the producers and the consumers, as well as the government, have important obligations on this subject.     

Stability of aflatoxin M in milk.

This three-part study was designed to determine aflatoxin M recovery from pasteurized and/or stored cow's milk. (a) Aflatoxin M was added to samples of raw Holstein milk at a concentration of 2.0 mug/liter. Half of each sample then was pasteurized at 63 C for 30 min, and both raw and pasteurized portions were stored at 4 C up to 17 days. (b) Samples of raw milk, pasteurized (77 C, 16 s) skim milk, dry cottage cheese curd, and cottage cheese whey were taken from a commercial operation in an area in which natural contamination had been encountered. (c) Milk from a cow dosed with aflatoxin B1 was stored frozen (-18 C) in bulk and in assay-size sample containers for 120 days. Aflatoxin M was recovered completely after either storage or pasteurization in (a) and (b). In (c), a recovery deficiency was detectable after 68 days of storage, which increased to 45% of the original value by 120 days. These observations differ from those of others in that loss of aflatoxin M was significant after pasteurization or storage of raw milk, totaling 87% loss after 120 days of frozen storage. Aflatoxin M partitioning between curd and whey in the preparation of cottage cheese agrees with more recent studies, but differs from previous reports. Three possible explanations for the differences are offered.     

Occurrence of aflatoxins M(1) and M(2) in milk commercialized in Ribeir?o Preto-SP, Brazil.

Aflatoxins are toxic metabolites found in foods and feeds. When ruminants eat foodstuffs containing aflatoxins B(1) and B(2), these toxins are metabolized and excreted as aflatoxin M(1) and M(2) in milk. The aim was to determine the incidence of these aflatoxins in commercial milk collected from supermarkets in Ribeir?o Preto-SP, Brazil, and consisting of 60 ultrahigh temperature (UHT) milk samples and 79 pasteurized milk samples. The milk samples were analysed according to method 986.16 of AOAC International. None of the milk samples analysed were contaminated with aflatoxin M(2), and aflatoxin M(1) was detected in 29 (20.9%) of samples in the range 50-240 ng l(-1). The results show that despite a high occurrence of aflatoxin M(1) in commercial pasteurized and UHT milk sold in Ribeir?o Preto in 1999 and 2000, the contamination level of these toxins could not be considered a serious public health problem according to MERCOSUR Technical Regulations. However, levels in 20.9% of the milk samples exceeded the concentration of 50 ng l(-1) permitted by the European Union. Although it is not necessary to continue monitoring the incidence and levels of aflatoxins M(1) and M(2) in milk samples, surveillance could be appropriate.     

Monitoring of warmed-over flavour in pork using the electronic nose – correlation to sensory attributes and secondary lipid oxidation products

Sensory analysis of meatballs was carried out to monitor the warmed-over flavour (WOF) development in cooked, cold-stored (at 4 °C for 0, 2 and 4 days) and reheated meatballs derived from M. longissimus dorsi (LD) and M. semimembranosus (SM) of pigs fed a standard diet supplemented with either 3% of rapeseed oil or 3% of palm oil. This was performed in combination with measurement of volatile compounds using a solid-state-based gas sensor array system (electronic nose) and gas chromatography/mass spectrometry together with measurement of thiobarbitoric acid reactive substances (TBARS). Subsequently, to elucidate the relations and predictability between the obtained data, the gas sensor responses were correlated with chemical (volatile and non-volatile secondary lipid oxidation products) and sensory data (flavour and odour attributes), using partial least squares regression modelling (PLSR). The TBARS, hexanal, pentanal, pentanol and nonanal all correlated to the sensory attributes associated to WOF formation. Moreover, the responses from eight of the MOS (metal oxide semiconductor) sensors within the electronic nose proved to be significantly related to WOF characteristics detected by both sensory and chemical analysis, while six of the MOSFET (metal oxide semiconductor field effect transistor) sensors were related to freshly cooked meat attributes determined by sensory analysis. The obtained results show the potential of the present gas sensor technology to monitor WOF formation in pork.     

Application of the electronic nose to the identification of different milk flavorings

In this paper, studies were conducted to determine the odor profile feature of five commercial milk flavorings (three natural milk flavorings and two synthetic flavorings) and one self-made enzyme induced milk flavoring prepared by lipolyzed milk fat. The discrimination of different flavor analysis methods was also evaluated. The ability of an electronic nose consisting of 18 metal oxide semiconductor (MOS) sensors to correlate with the solid phase micro extraction gas chromatography mass spectrometry (SPME-GC–MS) analysis and the sensory test of different milk flavorings was determined. The principal component analysis (PCA) of electronic nose sensor data has been compared with the data provided by GC–MS and sensory analysis. The results indicate that the electronic nose sensors can clearly and rapidly distinguish the difference among the synthetic milk flavorings, the natural milk flavorings and the enzyme induced milk flavoring. And the discrimination among different natural milk flavorings, which were easily confused by sensory tests, was also well performed by the electronic nose.     

Detection of mastitic milk using a gas-sensor array system (electronic nose)

Milk from mastitic and healthy reference quarters of dairy cows with acute clinical mastitis, and milk from healthy cows, were analysed using a gas-sensor array system (electronic nose) in two experiments using different incubation temperatures. Volatile components in the milk were also analysed by dynamic headspace gas chromatography–mass spectrometry (GC–MS). The results indicated that mastitic milk from cows with acute clinical mastitis could be separated from healthy milk using gas metal oxide semiconductive field effect transistors sensor array technology in combination with a CO₂ sensor. The discrimination between samples was better when incubating the samples at 60 °C than when incubating at 40 °C. The GC–MS identified the volatile substances in mastitic milk mainly as sulphides, ketones, amines and acids, while both milk from healthy reference quarters in mastitic cows and milk from healthy cows was characterised by products of lipid oxidation.     

Application of a microbial sensor for determination of short-chain fatty acids in raw milk samples.

A microbial sensor system, based on the use of immobilized Arthrobacter nicotiana and an oxygen electrode, was applied to determine free short-chain fatty acids in raw milk samples and the result was compared with gas chromatography (GC) and a titrimetric method. The sensor response was linearly related to the concentration of short-chain fatty acids obtained by GC (n = 10, r = 0.92) and to the total concentration of free fatty acids obtained by titrimetric measurement (n = 10, r = 0.78). This result suggests that the present microbial sensor can selectively determine free short-chain fatty acids in raw milk samples and may be useful as a very fast detection method of rancidity in milk.     

Detection, occurrence, and characterization of Escherichia coli O157:H7 from raw ewe's milk in Spain

A study was carried out in the Castilla y León region of Spain to investigate the presence of Escherichia coli O157:H7 in raw ewe's milk samples collected from several cheese factories during 1 year. All specimens were examined for E. coli O157:H7 by selective enrichment at 41.5 +/- 1.0 degrees C, after both 6 and 22 h of incubation, and then immunomagnetically separated and plated on cefixime-potassium tellurite-sorbitol MacConkey agar. No growth was obtained in the enrichment broth after a 6-h incubation. Presumptive colonies obtained after 22 h of incubation were screened by a multiplex PCR assay for the presence of rfbO157 and fliCH7 genes. Of all the ewe's milk samples studied, three were positive for E. coli O157:H7. The E. coli O157:H7 strains that were positive for the rfbO157 and fliCH7 genes were then analyzed by multiplex PCR for the presence of virulence genes (stx1, stx2, ehxA, and eaeA). All E. coli O157:H7 isolates were Shiga toxigenic and harbored additional genes related to virulence (ehxA and eaeA). The predominant Stx toxin type was stx2. These results demonstrate that raw ewe's milk used in cheesemaking may be sporadically contaminated with E. coli O157:H7 strains that are potentially pathogenic for humans.     

Enumeration and confirmation of Aeromonas hydrophila, Aeromonas caviae, and Aeromonas sobria isolated from raw milk and other milk products in Northern Greece.

A total of 138 raw cow's and 57 raw ewe's milk samples; 80 pasteurized cow's milk samples; 39 Anthotyros cheese, 36 Manouri cheese, and 23 Feta cheese samples; and 15 rice pudding samples were examined for the presence and any countable population of Aeromonas species. Twenty-two (15.9%) of the 138 cow's milk samples analyzed were contaminated with A. hydrophila. In 13 of these samples, populations of 3.0x10(2) to 5.0x10(3) CFU/ml were counted in starch ampicillin agar (SAA). Eighteen cow's milk samples (13.0%) were contaminated with A. caviae, and in eight of these samples, populations of 2.0x10(2) to 3.0x10(3) CFU/ml were counted in SAA. Five cow's milk samples (3.6%) were contaminated with A. sobria, and in two of these samples, populations of 2.5x10(3) and 5.0x10(3) CFU/ml were counted in SAA. Eleven cow's milk samples (7.9%) were contaminated with other Aeromonas spp. not classified. Eight (14.0%) of the 57 ewe's milk samples analyzed were contaminated with A. hydrophila. In these samples, populations of 5.0x10(2) to 5.0x10(3) CFU/ml were counted in SAA. Six ewe's milk samples (10.5%) were contaminated with A. caviae, and populations of 1.5x10(2) to 1.0x10(3) CFU/ ml were counted in SAA. Two ewe's milk samples (3.5%) were contaminated with A. sobria, and populations counted in SAA were 5.0x10(2) and 1.0x10(3) CFU/ml. Four samples (7.0%) were contaminated with other Aeromonas spp. not classified. A. hydrophila was recovered in 4 (10.2%) and 3 (8.3%) of the Anthotyros and Manouri cheese samples analyzed, respectively, but no countable populations were noted in SAA. None of the pasteurized milk, Feta cheese, and rice pudding samples yielded Aeromonas spp. The results of this work indicate that motile Aeromonas are common in raw milk in Greece. Also, the presence of A. hydrophila in the whey cheeses Anthotyros and Manouri indicates that postprocessing contaminations of these products with motile Aeromonas may occur during production.     

Evaluation of the quality of postharvest rapeseed by means of an electronic nose

BACKGROUND: Rapeseed is a valuable source of edible oil. The presence of even a small amount of mouldy or burnt rapeseed in a particular production batch deteriorates the quality of the edible oil obtained from it. Since the traditional method of using a panel of experts is time‐consuming, there is a need for fast and easy methods for rapeseed quality evaluation by intelligent devices to replace human labour. RESULTS: For rapeseed quality evaluation, an electronic nose equipped with an array of eight quartz microbalance sensors and four metal oxide semiconductor sensors was used. Signals generated by the sensors were analysed by principal component analysis and discriminant function analysis. Identification of samples that contained small proportions of mouldy or burnt rapeseed was possible despite the differences between the particular varieties studied. CONCLUSION: Electronic nose technology has shown the possibility of detecting samples of faulty rapeseed at very low contamination levels and distinguishing them with high probability from sound rapeseed. Copyright © 2012 Society of Chemical Industry     

Classification of Pecorino cheeses using electronic nose combined with artificial neural network and comparison with GC–MS analysis of volatile compounds

An electronic nose based on an array of 6 metal oxide semiconductor sensors was used, jointly with artificial neural network (ANN) method, to classify Pecorino cheeses according to their ripening time and manufacturing techniques. For this purpose different pre-treatments of electronic nose signals have been tested. In particular, four different features extraction algorithms were compared with a principal component analysis (PCA) using to reduce the dimensionality of data set (data consisted of 900 data points per sensor). All the ANN models (with different pre-treatment data) have different capability to predict the Pecorino cheeses categories. In particular, PCA show better results (classification performance: 100%; RMSE: 0.024) in comparison with other pre-treatment systems.     

Occurrence of Aflatoxin M1 in raw and processed milk and assessment of daily intake in Lahore,Multan cities of Pakistan

In this survey aflatoxin, M₁ was quantified in raw and processed milk from various areas of two big cities of Punjab province, i.e. Lahore and Multan. The results indicated that approximately 90% of the raw milk samples collected from Lahore city was contaminated with aflatoxin M₁. Similarly, around 92% of the raw milk samples collected from Multan city was contaminated with aflatoxin M₁. All samples of processed milk and tea whiteners were contaminated and 56% of the contaminated processed milk samples and 66% of the contaminated tea whitener samples were violating the maximum limits. The dietary exposure data of AFM₁ among six different groups was calculated, which indicated that the male children population was the most vulnerable group to AFM₁, up to 6.68 ng L^?1 per day and the least affected one was the female group above 20 years of age with 1.13 ng L^?1 per day.