ABSTRACT
This study assessed saturated mineral oil hydrocarbons (MOSH) and aromatic mineral oil hydrocarbons (MOAH) levels in grower-finisher feeds for pigs supplemented with 5% crude palm oil (CP), crude olive pomace oil (COP), olive pomace acid oil (OPA), or a blend of CP and OPA (50:50, w/w); the contribution of the lipid source to that contamination; and the ability of pigs to accumulate MOH in back fat and loin tissues after 60 days of trial. MOSH and MOAH were analyzed with liquid chromatography (LC)-gas chromatography (GC)-flame ionization detection (FID) after sample preparation. Among the lipid sources, CP had the lowest MOH levels, but CP feeds showed the highest contamination. This, along with the different MOSH profiles, indicated the presence of more significant contamination sources in the feeds than the lipid source. The higher MOH contamination in CP feeds was reflected in the highest MOSH levels in pig back fat, whereas MOAH were not detected in animal tissues. Also, MOSH bioaccumulation in pig tissues was influenced by the carbon chain length. In conclusion, feed manufacturing processes can determine the MOSH contamination present in animal adipose tissues that can be included in human diets.
ABSTRACT
Fatty acids are present in many foods, either free or esterified. Their presence helps to characterize and classify the food. The nature of these fatty acids is also associated with the treatments applied. To assess the fatty acid profile of these matrices, extractions are carried out using different solvents that influence the nature and lipid profile. The subsequent derivatization of fatty acids to more volatile fatty acyl methyl esters (FAMEs) prior to determination of the fatty acid profile takes into account the nature of the extraction solvent. Thus, the present work proposes to determine the fatty acid profile by Gas Chromatography Flame Ionisation Detector (GC-FID) of two lipid extracts derivatized by the MeOH/KOH and Hexane/MeOH/MeOH-BF3 procedures. Freshly harvested Tetracarpidium conophorum nuts from fields in the Fombap locality were brought to the laboratory where they were boiled (95 °C; 30 min), shelled, cut into small cubes and dried for 48 h at 45 °C. The dried seeds were ground and the resulting paste macerated in hexane for 48 h. The liquid fraction obtained was concentrated using a rotavapor, and the lipid extracts were stored at -15 °C. The egusi pudding was obtained by mixing 100 g of egusi seed paste with 0.50 g of white Piper nigrum powders, then packed in bulrush leaves and steamed for 120 min. After cooking, the product was stored for 4 days at room temperature and reheated twice a day. At the end of the last day, the lipid fraction oil was extracted following the methodology of Bligh and Dyer [1], then concentrated and preserved as before. The lipid extracts were then methylated using MeOH/KOH and Hexane/MeOH/MeOH-BF3 methods before injection into a GC-FID equipped with a Stabil Wax®-DA column. Supelco's standard mix of 37 FAMEs was used to identify and quantify the fatty acids present in the various samples. The results obtained enable us to identify the different fatty acids according to the retention time of their corresponding FAMEs and to quantify them. The fatty acids obtained were classified as saturated and unsaturated (mono and polyunsaturated). These analyses showed that the rapid derivatization method (MeOH/KOH) identified the same number of fatty acids as the Hexane/MeOH/MeOH-BF3 method in the lipid extract from the egusi pudding, whereas the Hexane/MeOH/MeOH-BF3 method identified four more fatty acids in the lipid extract coming from Tetracarpidium conophorum. Although the number of fatty acids was similar, the derivatization method influenced the nature of the fatty acids in the egusi pudding lipid extract. Overall, polyunsaturated fatty acids were the most abundant in the different oils. Omega-3 were the majority subclass in Tetracarpidium conophorum nuts, while omega-6 were in egusi pudding. The derivatization method did not influence the majority fatty acid (alpha linolenic) in Tetracarpidium conophorum nuts, whereas derivatization with BF3 gave trans linoleic and KOH cis linoleic in egusi pudding. These results show that the choice of derivatization method for fatty acid profiling and quantification is very important and depends on the technique and extraction solvents used.
ABSTRACT
This study evaluated the effect of using olive pomace acid oil (OPAO) instead of crude palm oil (PO) or refined olive pomace oil (ROPO) on lipid composition, lipid oxidation, and quality of chicken meat. Broiler chickens were fed diets with 6% of PO, ROPO, or OPAO, and deboned legs with skin were sampled. Fresh and refrigerated (commercial conditions; 7 days) chicken meat samples were assessed for fatty acid (FA) composition, tocopherol (T) and tocotrienol (T3) content, lipid oxidative stability, 2-thiobarbituric acid (TBA) values, volatile compounds, color, and sensory acceptance. Using ROPO and OPAO led to meat richer in monounsaturated FAs and OPAO to lower α-T levels compared to PO. Oxidative stability, TBA values, volatile compounds, and overall acceptance of meat were not affected by diet. Refrigeration increased TBA values and some volatile compounds' concentrations, but it did not decrease redness or consumers' overall acceptance. Therefore, the OPAO used was an adequate fat source for chicken diets at 6%, as it produced dark meat lower in saturated FAs than PO without affecting lipid oxidation or overall acceptance. According to this, upcycling OPAO as an energy source in chicken diets would be possible, which can contribute to the sustainability of the food chain.
ABSTRACT
Acid oils (AO) are fat by-products of edible oil refining with a high energetic value, being an interesting option for a more sustainable aquaculture nutrition. This study was conducted to evaluate the effects of the partial replacement of fish oil (FO) in diets by two AO instead of crude vegetable oils on the lipid composition, lipid oxidation and quality of fresh European seabass fillets, and after their commercial refrigerated storage for 6 days. Fish were fed with five different diets, the added fat being FO (100%) or a blend of FO (25%) and another fat (75%): crude soybean oil (SO), soybean-sunflower acid oil (SAO), crude olive pomace oil (OPO), or olive pomace acid oil (OPAO). Fresh and refrigerated fillets were assessed for fatty acid profile, tocopherol (T) and tocotrienol (T3) composition, lipid oxidative stability, 2-thiobarbituric acid (TBA) value, volatile compound content, color, and sensory acceptance. Refrigerated storage did not affect T + T3 total content but increased secondary oxidation products (TBA values and volatile compound contents) in fillets from all diets. The FO substitution decreased EPA and DHA and increased T and T3 in fish fillets, but the recommended human daily intake of EPA plus DHA could still be covered with 100 g of fish fillets. Both a higher oxidative stability and a lower TBA value were found in SO, SAO, OPO, or OPAO fillets, obtaining the greatest oxidative stability in OPO and OPAO fillets. Sensory acceptance was not affected by the diet or the refrigerated storage, while the differences found in color parameters would not be perceived by the human eye. According to the oxidative stability and acceptability of flesh, SAO and OPAO are adequate replacements of FO as energy source in European seabass diets, which implies that these by-products can be upcycled, improving the environmental and economical sustainability of aquaculture production.
ABSTRACT
Workers at risk of exposure to uranium compounds should be monitored and their internal exposure quantified in terms of committed effective dose E(50) in mSv. In vitro bioassay methods can quantify uranium in urine and faeces at low activity levels. Alpha spectrometry (AS) is the most common method used for monitoring alpha-emitting radionuclides in internal dosimetry services. It provides isotopic information and low minimum detectable activity (MDA) values (≤0.50 mBq per sample). This study reports the results of a five-year monitoring of workers exposed to uranium at a Spanish Juzbado facility, which produces nuclear fuel elements enriched with up to 5 % of 235U. Monitoring included about 100 workers per year, most of whom had worked at the facility for more than 10 years before the individual monitoring programme was established. We analysed nearly 550 samples of more than 200 workers over five years. The obtained results indicate that workers were adequately protected from uranium exposure through inhalation and had an acceptably low chronic intake at the facility.
