Chrysin loaded novasomes for enhanced wound healing management: In-vitro/ in-vivo evaluation

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Delivery Science and Technology Pub Date : 2025-04-01 DOI:10.1016/j.jddst.2025.106886
Abeer Salama , Asmaa Badawy Darwish , Rania Elgohary , Marwa Anwar Wagdi
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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.

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用于增强伤口愈合管理的含Chrysin的novasome:体外/体内评估
本研究的目的是开发和评估装载有Chrysin (CR)的novasome (NOVs)对伤口愈合的有效管理。采用薄膜水化技术制备了Chrysin Novasomes (CR-NOVs)。用胆固醇、油酸和3种不同浓度的非离子表面活性剂(Span 60、Span 40和Tween 80)制备了囊泡。CR- novs具有较高的CR EE%,范围为94.31±1.35 ~ 99.76±0.12%。囊泡大小在214.5±1.4 ~ 493.4±9.8 nm之间。所制备的nov具有−16.4±4.96 ~−33.2±3.45的负zeta电位,具有良好的稳定性。透射电镜(TEM)显示,优化后的囊泡呈球形。NOVs的CR释放呈双相过程,通过扩散机制符合Higuchi模型。局部应用CR-NOVs 10天,通过提高胶原蛋白和α-平滑肌肌动蛋白(α-SMA)的合成,以及增加组织金属蛋白酶抑制剂-1 (TIMP-1),减少创面大小,促进创面愈合活性。此外,CR-NOVs通过靶向基质金属蛋白酶(MMP2)减轻了细胞外基质(ECM)的降解。这些发现表明,所创建的CR-NOVs可能是一种独特的治疗方法,通过增加胶原和α-SMA来影响再上皮,从而缩短伤口愈合过程的时间。
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来源期刊
CiteScore
8.00
自引率
8.00%
发文量
879
审稿时长
94 days
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.
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