Sustained Release of Drug Facilitated Through Chemically Crosslinked Polyvinyl Alcohol-Gelatin (PVA-GE) Hydrogels. A sustainable biomedical approach
Author:
Ali Shaukat1, Ranjha Nazar Muhammad1, Ahmad Bashir2, Khan Ayaz Ali3, Hassan Fakhr Ul4, Aziz Tariq5, Alharbi Metab6, Alshammari Abdulrahman6, Alasmari Abdullah F.6, Alharbi Mousa Esa7
Affiliation:
1. 1 Department of Pharmacy , Bahauddin Zakariya University Multan, Punjab , Pakistan 2. 2 Department of Zoology , University of Malakand , Chakdara, 18800, Khyber Pakhtunkhwa , Pakistan 3. 3 Department of Biotechnology , University of Malakand , Chakdara, 18800, Khyber Pakhtunkhwa , Pakistan 4. 4 Faculty of Rehabilitation and Allied Health Sciences , Riphah International University , Islamabad Pakistan 5. 5 Department of Agriculture , University of Ioannina , Arta , Greece 6. 6 Department of Pharmacology and Toxicology, College of Pharmacy , King Saud University , P.O. Box 2455, Riyadh 11451 , Saudi Arabia 7. 7 Ministry of Health , Kingdom of Saudi Arabia , Riyadh , Saudi Arabia
Abstract
Abstract
The present study aimed to prepare hydrogel based on polyvinyl alcohol (PVA) and gelatin (Ge) and characterization of PVA/Ge hydrogel for their potential use as a sustained drug delivery system. Polyvinyl Alcohol (PVA) and-Gelatin (Ge) were cross-linked using glutaraldehyde (GA) as a crosslinking agent and hydrochloric acid (HCl) as a catalyst. Different feed polymer ratio and crosslinking agent concentration were used to prepare a series of PVA/Ge hydrogels. The obtained PVA/Ge hydrogels were investigated for dynamic and equilibrium swelling studies. The effect of polymers ratio, degree of crosslinking and pH of the medium on swelling of PVA/Ge hydrogels was investigated. Furthermore, the values of diffusion coefficient (D), volume fraction, polymer-solvent interaction parameter, molecular weight between crosslink and crosslink density were calculated. For swelling studies, 0.05M USP phosphate buffer solutions of different pH (1.2, 5.5, 6.5 and 7.5) were used. For the drug release study, ciprofloxacin HCl was loaded into selected samples as a model drug. The release of drug from these samples was performed for 12 hours in USP phosphate buffers of pH 1.2, 5.5 and 7.5. The release data from these samples were fitted into various kinetic models like zero order, first order, Higuchi and Peppas models to investigate the release mechanism. It was found that by varying the composition of PVA/Ge hydrogel and GA concentration, a significant difference was observed in drug release kinetics. FTIR spectroscopy and X-ray diffraction were used for the characterization of hydrogels. PVA/Ge hydrogel showed sustained release of the model drug at various pH values suggesting its potential use as a sustained drug delivery system.
Publisher
Walter de Gruyter GmbH
Subject
General Chemical Engineering,General Chemistry,Biotechnology
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