Journal
COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 103, Issue -, Pages 538-543Publisher
ELSEVIER
DOI: 10.1016/j.colsurfb.2012.10.042
Keywords
Spherical carbon adsorbent; Kremezin; Generic drug; Adsorption equilibrium; Adsorption kinetics; Adsorption mechanism
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The kinetic and mechanistic profiles of three pharmaceutical spherical carbon adsorbents, Kremezin as the brand product and two generics (Merckmezin and spherical carbon adsorbent Mylan), were compared. Five non-ionic active pharmaceutical ingredients with molecular weights of 136.1-424.1 Da were used as adsorbates. The results of Boehm titration, the standard method to qualify acidic or basic functional groups on a carbon surface, suggested distinctly different quantitative characteristics of each functional group among the three adsorbents. But those differences do not affect the adsorption to non-ionic adsorbates. The amount of theophylline adsorbed at equilibrium and surface area well correlated, suggesting that adsorptive ability was defined by surface area. In the tested molecular weight range, the order in terms of adsorption kinetics was spherical carbon adsorbent Mylan>Kremezin > Merkmezin. The adsorption profile in the equilibrium and kinetic experiments, and the lack of an effect of pH on adsorption quantity suggested that the mechanism of adsorption for non-ionic substances to be Langmuir type monolayer adsorption. Kremezin and spherical carbon adsorbent Mylan are more likely to adsorb co-administered drugs than Merckmezin. (C) 2012 Elsevier B.V. All rights reserved.
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