Monday, May 27, 2019

Lipids: Fatty Acid and Amp

The measurement of parameters much(prenominal) as anoint and fat content help define product quality for many another(prenominal) agricultural and food products. These values are widely used to determine energy content and to calculate the proportions of other food components. In addition oil and fat content significantly affect the texture, perceived quality and the flavour of products. (Whitney, Rolfes, Crowe, Cameron- Smith, & Walsh, 2011).An accurate and precise quantitative and qualitative analysis of lipids in food is significant for accurate nutritional labelling, determination of wether food meets standard identity, and to ensure that the product meets manufacturing specifications (Nielsen, 2010). AOAC International (2007) state the sample preparation for the lipid analysis depends on the character of food and the nature of the lipids in the food. Several preparatory steps are common in lipid analysis. They act to aid extraction by remotion of water, reduction of partic le size, or separation of the lipid from bound proteins or carbohydrates (Min &Ellefson, 2010).To analyse lipids it is necessary to first isolate them quantitatively from nonlipid components. Extraction of lipids from source materials, such as food, animal and plant tissues or microorganisms essay writer uk, should be carried out in a manner that avoids changes in the lipids or leads to formations of artefacts (Christie, 1993). It mightiness be necessary to deactivate enzymes that might hydrolyse lipids via heat treatment. (Vain, & Nairn, & Reid, 1991). Precaution must be taken to minimise oxidation of lipids, especially those with polyunsaturated fatty acids.Use of antioxidants might prove beneficial when dealing with extractions of lipids with highly unsaturated fatty acids (Carapace &Garcia, 2000). Carapace et al, (2000) state the accuracy of direct firmness extraction methods greatly depends on the solubility of the lipids in the solvent used and the ability to separate the l ipids from complexes with other macromolecules. The lipid content in food determined by extraction with one solvent may be quite different from the content determined with another solvent of different polarity.Fisheries and Aquaculture department (1986) concluded that solvent extraction techniques are usually used for the determination of fat content. However they tend to be slow, cumbersome, and require highly skilled personnel. In addition, many of the often-hazardous chemicals used are becoming more and more unacceptable according to international environmental standards. Despite these issues, solvent extraction continues to be used as a reference measurement for quality control. Nielsen (1994) admit the validity of the fat analysis of a food depends on sampling and the preservation of the sample before analysis.An ideal sample should be as weedy as possible to its intrinsic properties to the material from which it was taken. Pomeranz and Meloan (1994) states a sample is cons idered satisfactory if the properties under investigation correspond to those of the bulk material within the limits of the test. Min and Ellefson (2010) strike out organic solvent methods, which include Goldfish a continuous method, Soxhlet as a semicontinuous method and Folch as a discontinuous method are normally used to determine the total lipid content of food.They also note the major uses of these methods include extracting the fat prior to GC analysis, quality control of hypothecate products, determination of fat content in product development, verifying when fat content is

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