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Physicomechanical characterizations and in vitro release studies of electrospun ethyl cellulose fibers, solvent cast carboxymethyl cellulose films, and their composites. | LitMetric

AI Article Synopsis

  • Frequent changing of wound dressings can lead to inflammation and infections, which this study aims to address by creating special drug-loaded wound dressings.
  • Researchers created two types of drug-loaded materials: PHT-loaded ethyl cellulose (EC) microfibers that release medication slowly, and TCH-loaded carboxymethyl cellulose (CMC) films that release it quickly.
  • The study found that the combination of these materials can be designed to release drugs at different rates, enhancing the effectiveness and convenience of wound care.

Article Abstract

Frequent change of wound dressings introduces wound inflammation and infections. In this study, we electrospun phenytoin (PHT) loaded ethyl cellulose (EC) microfibers and solvent cast tetracycline hydrochloride (TCH) loaded carboxymethyl cellulose (CMC) films with the aim to demonstrate tailorable in vitro drug release behaviors suitable for long-term use of wound dressings. Results from tensile testing showed a significant decrease in average elastic moduli from 8.8 ± 0.6 to 3.3 ± 0.3 MPa after incorporating PHT into EC fibers. PHT-loaded EC fibers displayed a slow and zero-ordered release up to 80 % of the total drug at 48 h, while TCH-loaded CMC films demonstrated a rapid and complete release within 30 min. Furthermore, drug-loaded EC/CMC composites were fabricated into fiber-in-film and fiber-on-film composites. Fiber-in-film composites showed stage release of TCH and PHT at 8 h, while fiber-on-film composites demonstrated simultaneous release of PHT and TCH with a prolonged release of TCH from CMC films. In general, electrospun PHT-loaded EC microfibers, solvent cast TCH-loaded CMC films, and their composites were studied to provide a fundamental scientific understanding on the novelty of the ability to modulate drug release characteristics based on the composite designs.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2024.131374DOI Listing

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