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Traditionally, orally administered vitamins and drugs have low bioavailability, meaning that the product loses potency while it is being metabolized, before it is absorbed by the cells in the body Liposomal delivery takes this a step further by mimicking the structure of a cell membrane
Kesavardhana S, Malireddi R, Kanneganti TD
The amino group of the cysteine residue is then acetylated by the intracellular N-acetyltransferase enzymes and thereby forms the mercapturic acid which, depending on its characteristics, is rapidly led to circulation, bile, urine or metabolized until it is eliminated (Figure 3) [22]
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Arindrarto W, et al
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