4.7 Article

Formulation of pH-responsive highly swellable hydrogel scaffolds for controlled release of tramadol HCl: characterization and biocompatibility evaluation

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2023.1190322

Keywords

controlled delivery; polymeric; pH responsive; tramadol HCL; controlled drug delivery; toxicity studies

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The aim of this study was to develop a controlled delivery system for Tramadol HCl (TRD), an opioid analgesic used for moderate to severe pain. A pH-responsive hydrogel network was formulated using natural polymers, aloe vera gel and tamarind gum, monomer and crosslinker. The hydrogels showed pH sensitivity and exhibited a maximum release of 92.22% of TRD over 24 hours at pH 7.4.
Introduction: The objective of current project was to formulate a system for controlled delivery of Tramadol HCl (TRD), an opioid analgesic used in the treatment of moderate to severe pain.Methods: For this purpose, a pH responsive AvT-co-poly hydrogel network was formulated through free radical polymerization by incorporating natural polymers i.e., aloe vera gel and tamarind gum, monomer and crosslinker. Formulated hydrogels were loaded with Tramadol HCl (TRD) and evaluated for percent drug loading, sol-gel fraction, dynamic and equilibrium swelling, morphological characteristics, structural features and in-vitro release of Tramadol HCl.Results and Discussions: Hydrogels were proved to be pH sensitive as remarkable dynamic swelling response ranging within 2.94g/g-10.81g/g was noticed at pH 7.4 as compared to pH 1.2. Percent drug loading was in the range of 70.28%-90.64% for all formulations. Thermal stability and compatibility of hydrogel components were validated by DSC analysis and FTIR spectroscopy. Controlled release pattern of Tramadol HCl from the polymeric network was confirmed as maximum release of 92.22% was observed for over a period of 24 hours at pH 7.4. Moreover, oral toxicity studies were also conducted in rabbits to investigate the safety of hydrogels. No evidence of any toxicity, lesions and degeneration was reported, confirming the biocompatibility and safety of grafted system.

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