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Several methods have been reported for measuring glutathione based on ultra-violet (UV) absorbance, fluorescence, spectrophotometry, electrochemical and tandem mass spectroscopy, usually after protein precipitation in biological samples [31,32,33,34,35,36], all of which have limitations

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vulgare exhibited in vitro inhibitory activity in the nucleation and aggregation of calcium oxalate crystals, and also decreased the number of crystals produced in calcium oxalate metastable solutions