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Development of a cationic bacterial cellulose film loaded with anionic liposomes for prolonged release of oxacillin in wound dressing applications.

Authors :
Sedans KA
Stiegler Jurkevicz C
Silva BCC
Blener Lopes V
Lopes GFM
Schmitt EFP
Portes DB
Fronza M
Endringer DC
Tischer CA
Cabeça LF
Ferreira JMS
Ribeiro-Viana RM
Source :
International journal of pharmaceutics [Int J Pharm] 2024 Nov 15; Vol. 665, pp. 124649. Date of Electronic Publication: 2024 Sep 03.
Publication Year :
2024

Abstract

Dressings should protect wounds, promote healing, absorb fluids, and maintain moisture. Bacterial cellulose is a biopolymer that stands out in biomaterials due to its high biocompatibility in several applications. In the area of dressings, it is already marketed as an alternative to traditional dressings. However, it lacks any intrinsic activity; among these, the need for antimicrobial activity in infected wounds stands out. We developed a cationic cellulose film by modifying cellulose with 1-(5-carboxypentyl)pyridin-1-ium bromide, enhancing its wettability (contact angle: 26.6°) and water retention capacity (2714.37 %). This modified film effectively retained oxacillin compared to the unmodified control. Liposomal encapsulation further prolonged oxacillin release up to 11 days. Both oxacillin-loaded films and liposomal formulations demonstrated antimicrobial activity against Staphylococcus aureus. Our findings demonstrate the potential of chemically modified cellulose as a platform for controlled anionic antibiotics and/or their formulations delivery in wound care.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: [Renato Ribeiro Viana, Karina Andressa Sedans, Bruna Conceição Costa Silva, Cesar Augusto Tischer and Luis Fernando Cabeça have patent pending to BR10202202711. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper].<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-3476
Volume :
665
Database :
MEDLINE
Journal :
International journal of pharmaceutics
Publication Type :
Academic Journal
Accession number :
39236774
Full Text :
https://doi.org/10.1016/j.ijpharm.2024.124649