The alleged interaction of silica gel and ascorbic acid has been investigated in model experiments and in practical tablet trials, using wet granulation procedures. In simple mixtures stored for 3 weeks at 45° in closed tubes, losses of ascorbic acid increase progressively with increasing moisture content, whether or not silica gel is present, although losses are higher in the presence of silica gel. At an equivalent percentage of water in such mixtures, the amount of silica gel or the prior adsorption of 1 ½ times its weight of vitamin E on the silica gel, did not influence the loss of ascorbic acid. The data show that silica gel binds a certain fraction of the water present and that the loss of ascorbic acid is directly proportional to the amount of unbound water in the system. Sodium ascorbate is more sensitive than ascorbic acid to aerobic oxidation in the presence of moisture. Other commonly used tablet excipients, as well as silica gel, enhance losses of ascorbate. However, proper technology applied to wet granulation procedures yields excellent recoveries and stability of ascorbic acid or sodium ascorbate in dried granulations and in finished multivitamin tablets. The human bioassay technique, in which extra urinary excretion of ascorbic acid after tablet dosage is compared to that after dosage of ascorbic acid in water, has been used to demonstrate the full physiological availability of ascorbic acid in the presence of silica gel. Storage of such tablets for 3 months at 45° did not alter the complete bioavailability of the ascorbic acid.
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