Fabrication and In vitro Evaluation of Carbopol/Polyvinyl Alcohol-based pH-sensitive Hydrogels for Controlled Drug Delivery
Authors:
- 1 September 2023
- journal article
- research article
- Published by Bentham Science Publishers Ltd. in Current Pharmaceutical Design
- Vol. 29 (31) , 2489-2500
Abstract
Background:: Diclofenac sodium has a short half-life (about 1.5 hours), requiring repeated administration, and as a result, serious complications, such as GI bleeding, peptic ulcer, and kidney and liver dysfunction, are generated. Hence, a sustained/controlled drug delivery system is needed to overcome the complications caused by the administration of diclofenac sodium. Aims:: This study aimed to fabricate and evaluate carbopol/polyvinyl alcohol-based pH-sensitive hydrogels for controlled drug delivery. Objective:: pH-sensitive carbopol/polyvinyl alcohol graft-poly(acrylic acid) hydrogels (Cp/PVA-g-PAa hydrogels) were developed for the controlled delivery of diclofenac sodium. Methods:: The combination of carbopol/polyvinyl alcohol, acrylic acid, and ethylene glycol dimethacrylate was used as polymer, monomer, and cross-linker, respectively. The effects of the formulation’s composition on porosity, swelling index, and release pattern of diclofenac sodium from the developed hydrogels were investigated. Results:: An increase in porosity and swelling was observed with the increasing amounts of carbopol and acrylic acid, whereas polyvinyl alcohol showed the opposite effect. Due to the formation of a highly viscous system, the drug release decreased with the increasing concentrations of carbopol and polyvinyl alcohol while increased with increasing acrylic acid concentration. The pH-responsive properties of the fabricated hydrogels were demonstrated by dynamic swelling and drug release studies at three different pH values. Higher dynamic swelling and diclofenac sodium (model drug) release were found at high pH values compared to low pH values, i.e., pH 7.4 > 4.6 > 1.2, respectively. Cytotoxicity studies reported no toxic effect of the prepared hydrogels, thus indicating that the prepared hydrogels are safe to be used on clinical basis. Conclusion:: The prepared carbopol/polyvinyl alcohol crosslinked hydrogel can be used as a promising carrier for the controlled release of drugs.Keywords
Funding Information
- National Science Council of Taiwan (MOST 110-2320-B-037-014-MY2, NSTC 112-2320-B-037-014-MY3)
- An-Nan Hospital (ANHRF110-19)
This publication has 55 references indexed in Scilit:
- Synthesis of chemically cross-linked polyvinyl alcohol-co-poly (methacrylic acid) hydrogels by copolymerization; a potential graft-polymeric carrier for oral delivery of 5-fluorouracilDARU Journal of Pharmaceutical Sciences, 2013
- Electrospun diclofenac sodium loaded Eudragit® L 100-55 nanofibers for colon-targeted drug deliveryInternational Journal of Pharmaceutics, 2011
- Qualitative analysis of controlled release ciprofloxacin/carbopol 934 mucoadhesive suspensionJournal of Advanced Pharmaceutical Technology & Research, 2011
- Formulation, evaluation and optimization of stomach specific in situ gel of clarithromycin and metronidazole benzoate.International Journal of Drug Delivery, 2010
- HYDROGELS FROM ACRYLIC ACID WITH N,N-DIMETHYLACRYLAMIDE: SYNTHESIS, CHARACTERIZATION, AND WATER ABSORPTION PROPERTIESJournal of the Chilean Chemical Society, 2010
- Application of FTIR spectroscopy for structural characterization of ternary poly(acrylic acid)–metal–poly(vinyl pyrrolidone) complexesJournal of Applied Polymer Science, 2007
- Preparation, characterization, and water‐sorption study of polyvinyl alcohol based hydrogels with grafted hydrophilic and hydrophobic segmentsJournal of Applied Polymer Science, 2005
- Characterization of poly(vinyl alcohol)/poly(ethylene glycol) hydrogels and PVA-derived hybrids by small-angle X-ray scattering and FTIR spectroscopyPolymer, 2004
- Studies on drug release kinetics from ibuprofen–carbomer hydrophilic matrix tablets: influence of co-excipients on release rate of the drugJournal of Controlled Release, 1999
- A simple equation for the description of solute release. III. Coupling of diffusion and relaxationInternational Journal of Pharmaceutics, 1989