Heybet Kerem Polat, Sefa Gözcü, Sedat Ünal, Timur Paçacı, Eren Aytekin, Nasıf Fatih Karakuyu, Esra Köngül Şafak, Yakup Gültekin, Yonca Yazıksız, Nihat Kurt
{"title":"Gingerol containing polymeric nanofibers: a healing touch for accelerated wound recovery.","authors":"Heybet Kerem Polat, Sefa Gözcü, Sedat Ünal, Timur Paçacı, Eren Aytekin, Nasıf Fatih Karakuyu, Esra Köngül Şafak, Yakup Gültekin, Yonca Yazıksız, Nihat Kurt","doi":"10.1080/03639045.2024.2390033","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>In the current research, 6-gingerol (GA)-loaded <i>nanofiber drug delivery system</i> were developed, and their potential usage in wound healing was evaluated.</p><p><strong>Significance: </strong>This study investigates the effectiveness of nanofibrous membranes composed of sodium alginate (SA), poly(vinyl alcohol) (PVA), and 6-gingerol (GA) as delivery systems for anti-inflammatory agents in the context of wound dressings.</p><p><strong>Methods: </strong>GA-loaded SA/PVA nanofiber was prepared using electrospinning. <i>In vitro</i> characterization of this nanofiber included the examination of comprehensive <i>in vitro</i> characterization, anti-inflammatory and antioxidant activities, cytotoxicity, a scratch tes and <i>in vivo</i> skin test.</p><p><strong>Results: </strong>GA was extracted from <i>Zingiber officinale</i>, and its successful isolation was confirmed through analyses such as H-NMR, C-NMR. Then GA was electrospuned into the SA/PVA nanofibers, and scanning electron microscopy (SEM) imaging revealed that the fiber diameters of the formulations ranged between 148 nm and 176 nm. Anti-inflammatory and antioxidant studies demonstrated that the effectiveness of GA increased with higher doses; however, this increase was accompanied by decreased cell viability. In vitro release studies revealed that GA exhibited a burst release within the first 8 h, followed by a controlled release, reaching completion within 24 h. Within the scope of <i>in vitro</i> release kinetics, release data are mathematically compatible with the Weibull model with high correlation. The scratch test results indicated that TB2 (%1 GA) promoted epithelialization. Furthermore, it was determined that TB2 (%1 GA) did not cause any irritation.</p><p><strong>Conclusions: </strong>As a result, TB2 shows promise as a formulation for wound dressings, offering potential benefits in the field of wound care.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/03639045.2024.2390033","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: In the current research, 6-gingerol (GA)-loaded nanofiber drug delivery system were developed, and their potential usage in wound healing was evaluated.
Significance: This study investigates the effectiveness of nanofibrous membranes composed of sodium alginate (SA), poly(vinyl alcohol) (PVA), and 6-gingerol (GA) as delivery systems for anti-inflammatory agents in the context of wound dressings.
Methods: GA-loaded SA/PVA nanofiber was prepared using electrospinning. In vitro characterization of this nanofiber included the examination of comprehensive in vitro characterization, anti-inflammatory and antioxidant activities, cytotoxicity, a scratch tes and in vivo skin test.
Results: GA was extracted from Zingiber officinale, and its successful isolation was confirmed through analyses such as H-NMR, C-NMR. Then GA was electrospuned into the SA/PVA nanofibers, and scanning electron microscopy (SEM) imaging revealed that the fiber diameters of the formulations ranged between 148 nm and 176 nm. Anti-inflammatory and antioxidant studies demonstrated that the effectiveness of GA increased with higher doses; however, this increase was accompanied by decreased cell viability. In vitro release studies revealed that GA exhibited a burst release within the first 8 h, followed by a controlled release, reaching completion within 24 h. Within the scope of in vitro release kinetics, release data are mathematically compatible with the Weibull model with high correlation. The scratch test results indicated that TB2 (%1 GA) promoted epithelialization. Furthermore, it was determined that TB2 (%1 GA) did not cause any irritation.
Conclusions: As a result, TB2 shows promise as a formulation for wound dressings, offering potential benefits in the field of wound care.