{"title":"Chrysin loaded novasomes for enhanced wound healing management: In-vitro/ in-vivo evaluation","authors":"Abeer Salama , Asmaa Badawy Darwish , Rania Elgohary , Marwa Anwar Wagdi","doi":"10.1016/j.jddst.2025.106886","DOIUrl":null,"url":null,"abstract":"<div><div>The purpose of the study was to develop and evaluate novasomes (NOVs) loaded with Chrysin (CR) for the effective management of wound healing. Thin-film hydration technique was adopted for the preparation of Chrysin Novasomes (CR-NOVs). Vesicles were prepared employing cholesterol along with oleic acid and 3 types of non-ionic surfactants (Span 60, Span 40 and Tween 80) at different concentrations. CR-NOVs exhibited high CR EE%, ranging from 94.31 ± 1.35 to 99.76 ± 0.12 %. The vesicle size was between 214.5 ± 1.4 to 493.4 ± 9.8 nm. The prepared NOVs showed negative zeta potential values ranged from −16.4 ± 4.96 to −33.2 ± 3.45, confirming their good stability. Transmission electron microscopy (TEM) demonstrated that the optimized vesicles had a spherical shape. CR release from NOVs was biphasic, and the release behavior followed Higuchi's model through diffusion mechanism<strong>.</strong> Topical application of CR-NOVs for 10 days reduced wound size and promoted wound healing activity via elevating collagen and α-smooth muscle actin (α-SMA) synthesis as well as increasing tissue inhibitor of metalloproteinases-1 (TIMP-1). Additionally, CR-NOVs treatments alleviated extracellular matrix (ECM) degradation by targeting matrix metalloproteinases (MMP2). These findings suggest that the created CR-NOVs may be a unique treatment that affects re-epithelization by increasing collagen and α-SMA, hence reducing the time of the wound-healing process.</div></div>","PeriodicalId":15600,"journal":{"name":"Journal of Drug Delivery Science and Technology","volume":"108 ","pages":"Article 106886"},"PeriodicalIF":4.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Drug Delivery Science and Technology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1773224725002898","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
The purpose of the study was to develop and evaluate novasomes (NOVs) loaded with Chrysin (CR) for the effective management of wound healing. Thin-film hydration technique was adopted for the preparation of Chrysin Novasomes (CR-NOVs). Vesicles were prepared employing cholesterol along with oleic acid and 3 types of non-ionic surfactants (Span 60, Span 40 and Tween 80) at different concentrations. CR-NOVs exhibited high CR EE%, ranging from 94.31 ± 1.35 to 99.76 ± 0.12 %. The vesicle size was between 214.5 ± 1.4 to 493.4 ± 9.8 nm. The prepared NOVs showed negative zeta potential values ranged from −16.4 ± 4.96 to −33.2 ± 3.45, confirming their good stability. Transmission electron microscopy (TEM) demonstrated that the optimized vesicles had a spherical shape. CR release from NOVs was biphasic, and the release behavior followed Higuchi's model through diffusion mechanism. Topical application of CR-NOVs for 10 days reduced wound size and promoted wound healing activity via elevating collagen and α-smooth muscle actin (α-SMA) synthesis as well as increasing tissue inhibitor of metalloproteinases-1 (TIMP-1). Additionally, CR-NOVs treatments alleviated extracellular matrix (ECM) degradation by targeting matrix metalloproteinases (MMP2). These findings suggest that the created CR-NOVs may be a unique treatment that affects re-epithelization by increasing collagen and α-SMA, hence reducing the time of the wound-healing process.
期刊介绍:
The Journal of Drug Delivery Science and Technology is an international journal devoted to drug delivery and pharmaceutical technology. The journal covers all innovative aspects of all pharmaceutical dosage forms and the most advanced research on controlled release, bioavailability and drug absorption, nanomedicines, gene delivery, tissue engineering, etc. Hot topics, related to manufacturing processes and quality control, are also welcomed.