Biodegradable Gg-<i>cl</i>-poly(NIPAm-<i>co</i>-AA)/-<i>o</i>-MWCNT based hydrogel for combined drug delivery system of metformin and sodium diclofenac: <i>in vitro</i> studies
Pragnesh N. Dave, Pradip M. Macwan, Bhagvan Kamaliya
Abstract
at various pH levels and body temperatures. The structure and morphology of the produced hydrogel were characterised using FTIR spectra, SEM analysis, and drug loading tests. As a model drug, the hydrogel was loaded with metformin hydrochloride and sodium diclofenac (DS), and the medicines were released pH-dependently. To explore the drug release kinetics and mechanism, the zero order and first order kinetic models, the Korsemeyar-Peppas model, the Higuchi model, and the Hixson-Crowell model have all been employed. Drug release studies revealed notable characteristics in connection to physiologically predicted pH values, with a high release rate at pH = 9.2. At pH = 9.2, however, both metformin and sodium diclofenac exhibited a Fickian mechanism. Combination treatment may reduce the effective dose of a single drug and hinder metabolic rescue mechanisms. More study is needed to detect any negative effects on individuals.