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https://dspace.iiti.ac.in/handle/123456789/14256
Title: | N-Hydroxyalkanamide Based Organo/hydrogels as Novel Scaffolds for pH-Dependent Metronidazole and Theophylline Release |
Authors: | Sermadurai, Selvakumar |
Keywords: | Drug delivery;Gelation;Metronidazole;N-Hydroxyalkanamides;Theophylline |
Issue Date: | 2024 |
Publisher: | John Wiley and Sons Inc |
Citation: | Monika, Meenakshi, Brahma, M., Maruthi, M., Selvakumar, S., Ansari, A., & Gupta, M. K. (2024). N-Hydroxyalkanamide Based Organo/hydrogels as Novel Scaffolds for pH-Dependent Metronidazole and Theophylline Release. Chemistry and Biodiversity. https://doi.org/10.1002/cbdv.202400105 |
Abstract: | The traditional delivery of metronidazole and theophylline presents challenges like bitter taste, variable absorption, and side effects. However, gel-based systems offer advantages including enhanced targeted drug delivery, minimized side effects, and improved patient compliance, effectively addressing these challenges. Consequently, a cost-effective synthesis of N-hydroxyalkanamide gelators with varying alkyl chain lengths was achieved in a single-step reaction procedure. These gelators formed self-assembled aggregates in DMSO/water solvent system, resulting in organo/hydrogels at a minimum gelation concentration of 1.5 % w/v. Subsequently, metronidazole and theophylline were encapsulated within the gel core and released through gel-to-sol transition triggered by pH variation at 37 °C, while maintaining the structural-activity relationship. UV-vis spectroscopy was employed to observe the drug release behavior. Furthermore, in vitro cytotoxicity assays revealed cytotoxic effects against A549 lung adenocarcinoma cells, indicating anti-proliferative activity against human lung cancer cells. Specifically, the gel containing theophylline (16HAD+Th) exhibited cytotoxicity on cancerous A549 cells with IC50 values of 19.23±0.6 μg/mL, followed by the gel containing metronidazole (16HAD+Mz) with IC50 values of 23.75±0.7 μg/mL. Moreover, the system demonstrated comparable antibacterial activity against both gram-negative (E. coli) and gram-positive bacteria (S. aureus). © 2024 Wiley-VHCA AG, Zurich, Switzerland. |
URI: | https://doi.org/10.1002/cbdv.202400105 https://dspace.iiti.ac.in/handle/123456789/14256 |
ISSN: | 1612-1872 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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