Imen Trabelsi , Naourez Ktari , Wafa Gargouri , Sirine Ben Slima , Sana Bardaa , Amina Maalej , Lobna Jlaiel , Mohamed Chamkha , Riadh Ben Salah
{"title":"Characterization of a green-synthesized heteropolysaccharide with promising diabetic wound healing potential","authors":"Imen Trabelsi , Naourez Ktari , Wafa Gargouri , Sirine Ben Slima , Sana Bardaa , Amina Maalej , Lobna Jlaiel , Mohamed Chamkha , Riadh Ben Salah","doi":"10.1016/j.rechem.2025.102705","DOIUrl":null,"url":null,"abstract":"<div><div>Natural polysaccharides are increasingly explored for use in biomaterials, such as wound dressings, due to their excellent biocompatibility, low toxicity, and beneficial biomedical properties. This research investigates a natural polysaccharide hydrogel prepared using <em>Laurus nobilis</em> leaves (LNSP) and its <em>in vivo</em> potential to facilitate wound healing of a diabetic animal model. The results indicated a molecular weight of 105.37 kDa for the newly extracted polysaccharide. This heteropolysaccharide is composed of glucose (31.22 %), galactose (20.91 %), mannose (15.25 %), xylose (14.85 %), ribose (9.2 %), and rhamnose (8.57 %). Our findings showed that LNSP polysaccharide possesses antibacterial activity, acts as a potential antioxidant source, and exhibits no cytotoxic effects on human HEK-293 cells. In addition to displaying typical hydrogel characteristics, it also presents properties that promote wound re-epithelialization, replicate the structure of skin and stimulate skin regeneration in a diabetic rat model. Notably, it significantly improved the rate of wound contraction, reaching 100 % after 14 days. Histological assessment demonstrated that the LNSP hydrogel enhances re-epithelization and epidermal regeneration in diabetic rats compared to other treatment groups. This novel polysaccharide has been explored for dual applications: as a wound dressing and as a medium for direct drug delivery to the lesion site.</div></div>","PeriodicalId":420,"journal":{"name":"Results in Chemistry","volume":"18 ","pages":"Article 102705"},"PeriodicalIF":4.2000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211715625006885","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Natural polysaccharides are increasingly explored for use in biomaterials, such as wound dressings, due to their excellent biocompatibility, low toxicity, and beneficial biomedical properties. This research investigates a natural polysaccharide hydrogel prepared using Laurus nobilis leaves (LNSP) and its in vivo potential to facilitate wound healing of a diabetic animal model. The results indicated a molecular weight of 105.37 kDa for the newly extracted polysaccharide. This heteropolysaccharide is composed of glucose (31.22 %), galactose (20.91 %), mannose (15.25 %), xylose (14.85 %), ribose (9.2 %), and rhamnose (8.57 %). Our findings showed that LNSP polysaccharide possesses antibacterial activity, acts as a potential antioxidant source, and exhibits no cytotoxic effects on human HEK-293 cells. In addition to displaying typical hydrogel characteristics, it also presents properties that promote wound re-epithelialization, replicate the structure of skin and stimulate skin regeneration in a diabetic rat model. Notably, it significantly improved the rate of wound contraction, reaching 100 % after 14 days. Histological assessment demonstrated that the LNSP hydrogel enhances re-epithelization and epidermal regeneration in diabetic rats compared to other treatment groups. This novel polysaccharide has been explored for dual applications: as a wound dressing and as a medium for direct drug delivery to the lesion site.