Kocaaga, Banu and Güner, Fatma Seniha (2026) Influence of plasticizer type on the structure and drug release characteristics of LM-pectin hydrogels. Turkish Journal of Chemistry, 50 (1). pp. 1-11. ISSN 1300-0527 (Print) 1303-6130 (Online)
Influence.pdf
Available under License Creative Commons Attribution.
Download (4MB)
Official URL: https://dx.doi.org/10.55730/1300-0527.3775
Abstract
This study investigated the effects of different plasticizers—castor oil (CO), polyvinylpyrrolidone (PVP), and polyethylene glycol (PEG) with varying molecular weights (MWs)—on the structure and drug-release performance of low-methoxyl pectin (LM-pectin) hydrogels. Theophylline was used as a model drug to evaluate release behavior under physiologically relevant conditions. The incorporation of plasticizers modulated polymer–polymer interactions, swelling behavior, and thermal properties, thereby affecting drug-release kinetics. CO, a hydrophobic triglyceride, created microdomain-induced diffusion pathways; PVP, containing water-affinitive lactam units, facilitated moisture-driven plasticization; and PEG (MW 400/1000/1500), with hydroxyl-terminated chains, established hydrogen bonds with pectin. Structural analyses (FTIR and DSC) revealed that CO disrupted pectin packing, leading to a flexible yet crystalline matrix and enabling the highest cumulative drug release. PVP-based hydrogels exhibited enhanced crystallinity and slower release, whereas PEG formulations showed molecular-weight-dependent behavior. Kinetic calculations confirmed similar patterns, demonstrating non-Fickian transport for PEG400 and PEG1000 (diffusion associated with polymer relaxation) and an additional diffusion-limited profile for PEG1500 attributed to network densification. Among the methods evaluated, CO improved cumulative release, while PEG1500 and PVP promoted extended, lower-rate delivery. The selection of plasticizers must correspond with the design objective: CO for high cumulative release and PEG1500 or PVP for prolonged, diffusion-controlled administration. These results highlight the critical role of the plasticizer type in tailoring hydrogel performance. The LM-pectin formulations developed herein demonstrate potential for application in controlled dermal and mucosal drug-delivery systems.
| Item Type: | Article |
|---|---|
| Additional Information: | This work is licensed under a Creative Commons Attribution 4.0 International License. This Research Article is brought to you for free and open access by TÜBİTAK Academic Journals. |
| Uncontrolled Keywords: | controlled release; drug release kinetics; hydrogel; LM-pectin; plasticizer |
| Divisions: | Sabancı University Nanotechnology Research and Application Center |
| Depositing User: | IC-Cataloging |
| Date Deposited: | 16 Apr 2026 17:03 |
| Last Modified: | 16 Apr 2026 17:03 |
| URI: | https://research.sabanciuniv.edu/id/eprint/53836 |

