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Biomedical subjects

A Huyghebaert

Publications and source records attributed to A Huyghebaert.

At least 19 recordsLinked to original sources

On-farm contamination of animals with chemical contaminants.

Food products should not contain unsafe levels of chemical contaminants. However, it is not possible to monitor each and every one of the many thousands of chemicals that are used in our advanced societies. Chemical contaminants in foodstuffs of animal origin may be classified into three categories: natural contaminants (e.g. mycotoxins), environmental contaminants linked to industrialisation and/or urbanisation (e.g. dioxins and dioxin-like compounds) and authorised chemical products (e.g. residues of veterinary medical products). Chemical hazards may contaminate foodstuffs of animal origin all the way from farm to fork. Contamination may occur in any of the different production systems, and it is difficult to make comparisons between production systems (e.g. extensive versus intensive farming systems) with regard to food safety. Even when we take into account the latest analytical methods, which can detect ever-smaller quantities of residues, the relative importance of chemical contaminants seems to have declined during recent decades due to improvements in information and prevention. Nonetheless, individual incidents can never be ruled out and may have serious economic, health or social repercussions. Particular attention must be paid to chemical hazards, in order to reduce as much as possible the risks to livestock and to the consumer. Continued monitoring and periodic reassessment of risks posed by these contaminants (at the national level) are needed to detect or anticipate new problems, so that appropriate actions can be taken in the interest of public health. More attention should be paid to the production of detailed information, especially with regard to background data (e.g. the objectives of the monitoring, sampling methods, chemicals to be analysed, analytical methods, detection limits, raw data and specified units), in order to obtain a better basis for risk assessment. Such risk assessment provides control authorities with an effective tool for the exchange of information and measures to be taken to ensure food safety.

Animal Husbandry↗

Protective influence of several packaging materials on light oxidation of milk.

Light-induced degradation reactions in milk create a serious problem for the dairy industry because of the development of off-flavors, the decrease in nutritional quality, and the severity and speed by which these phenomena develop. Packaging materials are essential to avoid this particular deterioration of milk. Therefore, efforts are being made to design protective polyethylene terephthalate (PET) packages. In the present study, a number of PET bottles were compared for their ability to avoid photo-oxidation in UHT semi-skimmed milk. The milk was packed in 3 types of PET bottles: one transparent bottle provided with an active oxygen-binding inner layer, one bottle with perfect light barrier, and one transparent bottle provided with a UV-absorbing additive. During 2 storage experiments, running parallel to each other for 2 mo, chemical milk quality parameters such as fat oxidation, vitamin and protein degradation, oxygen consumption, and color change were monitored. A trained taste panel compared the sensory quality of the illuminated milk stored in these bottles, with milk perfectly protected against light and oxygen. In the first study, milk was continuously illuminated at room temperature. A comparison was made for milk under storage conditions that simulated those expected during display in retail and supermarkets. The results of the 2 shelf-life studies showed that an adequate light barrier was apparently sufficient to avoid the light-induced oxidation of milk during extended storage. Oxygen barriers, on the other hand, did not provide a significant protection, nor did bottles with UV filter. If wavelengths detrimental to riboflavin were not completely excluded by the packaging material, incoming light could still give rise to photo degradation of milk. Accordingly, riboflavin and vitamin A were gradually degraded, milk fat was photo-oxidized, oxygen dissolved in the milk was consumed, and the sensorial quality decreased significantly.

Animals↗

Gas chromatographic characterization of vegetable oil deodorization distillate.

Because of its complex nature, the analysis of deodorizer distillate is a challenging problem. Deodorizer distillate obtained from the deodorization process of vegetable oils consists of many components including free fatty acids, tocopherols, sterols, squalene and neutral oil. A gas chromatographic method for the analysis of deodorizer distillate without saponification of the sample is described. After a concise sample preparation including derivatization and silylation, distillate samples were injected on column at 60 degrees C followed by a gradual increase of the oven temperature towards 340 degrees C. The temperature profile of the oven was optimized in order to obtain a baseline separation of the different distillate components including free fatty acids, tocopherols, sterols, squalene and neutral oil. Good recoveries for delta-tocopherol, alpha-tocopherol, stigmasterol and cholesteryl palmitate of 97, 94.4, 95.6 and 92%, respectively were obtained. Repeatability of the described gas chromatographic method was evaluated by analyzing five replicates of a soybean distillate. Tocopherols and sterols had low relative standard deviations ranging between 1.67 and 2.25%. Squalene, mono- and diacylglycerides had higher relative standard deviations ranging between 3.33 and 4.12%. Several industrial deodorizer distillates obtained from chemical and physical refining of corn, canola, sunflower and soybean have been analyzed for their composition.

Chromatography, Gas↗

Modeling of alpha-tocopherol loss and oxidation products formed during thermoxidation in triolein and tripalmitin mixtures.

The degradation of alpha-tocopherol and the formation of alpha-tocopherol and triacylglycerol oxidation products at high temperatures (150-250 degrees C) over a heating period (0-4 h) for a model system ranging between triolein and tripalmitin were modeled by use of an experimental design. The oxidation products of alpha-tocopherol formed under these conditions were alpha-tocopherolquinone (1 .4-7.7%) and epoxy-alpha-tocopherolquinones (4.3-34.8%). The results indicate a very high susceptibility of alpha-tocopherol to capture peroxyl radicals upon oxidation, leading to the formation of polar tocopherol oxidation products. Both alpha-tocopherolquinone and epoxy-alpha-tocopherolquinones were not stable upon prolonged heating and were further degraded to other unknown oxidation products. The kinetics of alpha-tocopherol oxidation were significantly influenced by the triolein/tripalmitin ratio. By increasing the level of triacylglycerol unsaturation the rate of alpha-tocopherol recovery after heating increased significantly from 2.2 to 44.2% whereas in the meantime triacylglycerol polymerization increased from 0 to 3.7%.

Chromatography, High Pressure Liquid↗

Identification of alpha-tocopherol oxidation products in triolein at elevated temperatures.

The effect of high-temperature treatment on the stability of alpha-tocopherol (1) in triolein was assessed under a reduced-pressure atmosphere (4-40 mbar) simulating the deodorization step of the refining of vegetable oils. A marked degradation of 1 was observed, which increased with increasing temperature (180-260 degrees C) and heating time (20-80 min). The degradation of 1 in triolein at 240 degrees C was inhibited by the addition of the synthetic antioxidant TBHQ or when heating was performed under nitrogen atmosphere, indicating oxidative degradation. The oxidation products were isolated and identified as alpha-tocopherolquinone (2), 4a,5-epoxy-alpha-tocopherolquinone (3), and 7,8-epoxy-alpha-tocopherolquinone (4).

Antioxidants↗

Combined liquid and gas chromatographic characterisation of polyglycerol fatty acid esters.

In the present study a combined liquid and gas chromatographic technique is described for the analysis of polyglycerol fatty acid esters. Liquid chromatographic fractionation of samples resulted in pure standards of monoesters of di- and triglycerols and diesters of di- and triglycerols. Confirmation of their identity was achieved by LC-MS analysis. Moreover, a chromatographic identification of the mono- and diesters of cyclic diglycerol was proposed. From the isolation of pure esters and their gas chromatographic analysis, it was revealed that co-elution of several compounds occurred. Thus it was shown that prefractionation of the sample using a simplified liquid chromatographic separation, was necessary in order to characterise the esters correctly. In combination with some other chemical analyses, a complete profile of the chemical composition of polyglycerol fatty acid esters can be obtained.

Chromatography, Gas↗

Amino acid profiles after sprouting, autoclaving, and lactic acid fermentation of finger millet (Eleusine coracan) and kidney beans (Phaseolus vulgaris L.).

Seeds of finger millet (Eleucine coracan (L.) Gaertner) and kidney beans (Phaseolus vulgaris L.) were sprouted, autoclaved, and fermented during the processing of a weaning (complementary) food for children. Relative changes in individual amino acids with processing were evaluated. Finger millet and kidney beans both showed a good percentage of essential to total amino acids, with 44. 2-44.9% in finger millet and 44.2-45.1% in kidney beans, when compared to 33.9% for the FAO/WHO reference protein for 2-5 year old children. Sprouting resulted in a significant decrease in lysine in kidney beans. Autoclaving caused significant decreases in histidine, while fermentation significantly decreased phenylalanine and increased tryptophan in finger millet. The leucine-to-lysine ratio, which is an indicator of the pellagragenic character of a protein, was significantly improved in finger millet by both sprouting and fermentation.

Amino Acids↗

Effect of irradiation, packaging, and postirradiation cooking on the thiamin content of chicken meat.

The effect of irradiation with X rays or electrons, irradiation and storage temperature, and postirradiation cooking on the thiamin content of vacuum- or air-packaged minced chicken meat was examined. Samples irradiated with 3-kGy X rays (50 Gy/min) or electrons (5 kGy/min) contained less thiamin than the control specimens, but no differences between both irradiation methods were detected. The thiamin content in samples stored and/or irradiated at 5 degrees C was between 13 and 24 microg per 100-g product lower than in samples stored and/or ionized at -18 degrees C. The same difference in thiamin content was found for specimens packaged in a vacuum or air package, respectively. Vacuum packaging lead to a greater loss of drip than air-packaged samples. The biggest loss of thiamin, 31.1 and 28.0% for X rays and electron beams, respectively, was measured for vacuum-packaged specimens stored and irradiated at 5 degrees C. Compared with the cooked minced chicken breast meat, a higher thiamin content (6 to 17 microg of thiamin per 100-g product) was obtained for the raw samples. When irradiation and vacuum packaging were compared as two separate preservation techniques, the two methods had approximately the same effect on the thiamin content of the minced chicken meat. The mean temperature of the samples after cooking was 87.2 +/- 4.9 degrees C. However, significant differences in internal temperature after cooking of the samples were measured between air- and vacuum-packaged samples.

Animals↗

Polystyrene cups and containers: styrene migration.

The level of styrene migration from polystyrene cups was monitored in different food systems including: water, milk (0.5, 1.55 and 3.6% fat), cold beverages (apple juice, orange juice, carbonated water, cola, beer and chocolate drink), hot beverages (tea, coffee, chocolate and soup (0.0, 0.5, 1, 2, and 3.6% fat), take away foods (yogurt, jelly, pudding and ice-cream), as well as aqueous food simulants (3% acetic acid, 15, 50, and 100% ethanol) and olive oil. Styrene migration was found to be strongly dependent upon the fat content and storage temperature. Drinking water gave migration values considerably lower than all of the fatty foods. Ethanol at 15% showed a migration level equivalent to milk or soup containing 3.6% fat. Maximum observed migration for cold or hot beverages and take-away foods was 0.025% of the total styrene in the cup. Food simulants were responsible for higher migration (0.37% in 100% ethanol). A total of 60 food samples (yogurt, rice with milk, fromage, biogardes, and cheese) packed in polystyrene containers were collected from retail markets in Belgium, Germany, and the Netherlands. The level of styrene detected in the foods was always fat dependent.

Beverages↗

Screening of Salmonella in naturally contaminated feeds with rapid methods.

Five commercially available screening methods, the Oxoid MSRV, Merck SALMOSYST-RAMBACH AGAR combination, Organon Teknika SALMONELLA-TEKTM, Dynal DYNABEADS ANTI-SALMONELLA and Foss Electric EIAFOSS, were compared to the conventional culture procedure for the detection of Salmonella in naturally contaminated feed samples. A total of 217 feed samples from animal as well as from vegetable origin were examined. Twenty one samples were found to be positive for Salmonella by all methods combined. The conventional culture method detected 17 (81,0%), MSRV 19 (90,5%), SALMOSYST-RAMBACH 8 (38,1%), SALMONELLA-TEK 19 (90,5%), DYNABEADS ANTI-SALMONELLA 7 (33,3%) and EIAFOSS 21 (100%) of the 21 total Salmonella contaminated samples.

Animal Feed↗

Contribution of trans fatty acids from vegetable oils and margarines to the Belgian diet.

Nineteen commercial samples of vegetable oils and margarines marketed in Belgium (nine margarines, nineteen vegetable oils), Hungary (seven margarines) and Great Britain (three margarines) were analyzed by gas-liquid chromatography for their trans fatty acid (TFA) content. For the vegetable oil samples under study, the TFA content ranged from 0.0-4.6% (mean : 1.1%, S.D. : 1.1%). Trans isomers in these samples were almost exclusively C18:2 and C18:3 isomers formed during high temperature refining. Trans isomers of the margarines were mainly C18:1 isomers formed during hydrogenation. For the Belgian and Hungarian samples mean trans values of 6.36% (S.D.=6.20%) and 14.06% (S.D.=7.59%), respectively expressed on fat basis were established. From these figures, the average daily intake of TFA from margarines and vegetable oils by the Belgian population was calculated at 1.1 and 0.1g/person/day, respectively. When so-called zero-trans margarines (+/- 0.5% TFA) are consumed, the trans intake can be reduced to about 0.1g/person/day. Further studies leading to figures about the contribution of TFA from 'invisible fat' food products will be conducted in the near future.

Belgium↗

Determination of polycyclic aromatic hydrocarbons in fat products by high pressure liquid chromatography.

The method previously described by Gertz [1] for the extraction of 3,4-benzopyrene in meat- and fishproducts has been adapted for butter, margarine, edible oils and fats and extended to other polycyclic aromatic hydrocarbons (PAH): 1,2-benzopyrene, 1,2,3,4-dibenzanthracene, 1,2,5,6-dibenzanthracene and 1,12-benzoperylene. The isolated PAH are determined by high-pressure liquid chromatography on reversed-phase columns with detection by fluorimetry. Recoveries range from 76 to 85%. The detection limit varies between 0.10 and 0.90 ppb. By application of optimized analysis conditions the sensitivity can be increased to 0.01 ppb for each compound.

Benz(a)Anthracenes↗