Abstract

Clays and clay minerals have been widely used as carriers for drug delivery due to their properties such as cation exchange capacity, adsorption, and biocompatibility. In this study, a new drug release system was obtained by adsorption of amiloride hydrochloride on calcium bentonite (Ca2+-Bent). The ‘in vitro’ release tests were evaluated in the gastric (SGF, pH 1.2), and intestinal (SIF, pH 7.4) simulated fluids. The drug intercalation in clay mineral was confirmed by X-ray diffraction and transmission electronic microscopy, obtaining basal space of 1.59 nm in the hybrid. Zeta potential measurements, infrared spectroscopy, X-ray photoelectron spectroscopy, XRF and calcium release supported the mechanism of drug/clay mineral interaction. The amount of loaded amiloride on Ca2+-Bent was 192.3 mg per gram of solid and characterizations suggested the contribution of both ion exchange and Ca2+ drug complexation in the process. The Ca2+-Bent/amiloride hybrid exhibited a drug-controlled release and reached a release of 53.4% and 38.9% in 11 h in SGF and SIF fluids, respectively. MTT evaluation indicated that system was biocompatible. Ca2+-Bent behaved as a promisor for the drug delivery system.

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