Glutathione is a naturally occurring compound that plays a crucial role in the cellular response to oxidative stress through its ability to quench free radicals, thus mitigating the risk of potential damage, including cell death. While glutathione is endogenously present in different plants and animal cells, their concentration varies considerably. The alteration in glutathione homeostasis can be used as a potential marker for human diseases. In the case of the depletion of endogenous glutathione, exogenous sources can be used to replenish the pool. To this end, both natural and synthetic glutathione can be used. However, the health benefit of glutathione from natural sources derived from fruits and vegetables is still debated. There is increasingly growing evidence of the potential health benefits of glutathione in different diseases; however, the determination and in situ quantification of endogenously produced glutathione remains a major challenge. For this reason, it has been difficult to understand the bioprocessing of exogenously delivered glutathione in vivo. The development of an in situ technique will also aid in the routine monitoring of glutathione as a biomarker for different oxidative stress-mediated diseases. Furthermore, an understanding of the in vivo bioprocessing of exogenously delivered glutathione will also aid the food industry both towards improving the longevity and profile of food products and the development of glutathione delivery products for long-term societal health benefits. In this review, we surveyed the natural plant-derived sources of glutathione, the identification and quantification of extracted glutathione from these sources, and the role of glutathione in the food industry and its effect on human health.

The study contains the description of the ostrich fat by estimating the chemical content, which included moisture, protein, fat, ash, cholesterol, minerals and lipid-soluble vitamins, including vitamin (E andA) and the estimation of lipoproteins. Chemical properties were also studied which include peroxide value (PV), free fatty acids (FFA), saponification number (SN), iodine number and Physical properties include viscosity, density and specific gravity, refractive index, melting point and ester value (EV). Fatty acids were identified by using gas chromatography (GC). The results showed the percentage of moisture, protein, fat and ash were 5.56%, 5.16%, 87.88% and 1.03%, respectively. The mineral includes sodium, potassium, calcium, magnesium, phosphorus, iron and selenium reach to 8.5, 2.5, 40.11, 12.96, 78.6, 0.532 and 7.86 ppm respectively, cholesterol content was 50.63 mg / 100 g, vitamins content A and E was recorded 72.13 and 91.30 mg / ml respectively. The fat has good chemical and physical properties, such as viscosity, density and specific gravity, refractive index, melting point, saponification number, iodine number and ester value. While the results of lipoproteins in the ostrich fat HDL was 65 mg / dl, LDL 52 mg / dl and VLDL 35 mg / dl and triglycerides reach to 75 mg / dl. The peroxide number was 0.86 equivalent Meq O2 / Kg, and the percentage of the free fat acids reach to 0.38%. The fatty acid compassion was analyzed by gas chromatography (GC) and also showed nine saturated and unsaturated fatty acids including oleic acid, palmitic acid, arachidonic acid, erucic acid, heneicosanoic acid, undecanoic acid, lauric acid, caproic acid and myristic acid.

Carnosines were extracted from alkhshni fish Liza abu L. by using alcohol and water separation,Carnosines were identificated in several ways including spectroscopy identification using UV-visible and Fourier Transform infrared spectrophotometer technology and High Performance Liquid Chromatography (HPLC), spectral diagnostics using Ultraviolet-visible (UV) carnosines single peak showed at 215 nm wavelength and at diagnosis High Performance Liquid Chromatography (HPLC) retention time stood for standard carnosines 2.532 and author carnosines separated from 2.614 minutes alcoholic carnosines and 2.625 minutes aqueous carnosines, after undetecting the detection of toxicity assay of carnosines prepared on human blood serum and there have been no changes in its shape and appearance.

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