| Literature DB >> 27485953 |
Guanzhe Xu1, Liang Cheng2, Qintong Zhang1, Yunlong Sun1, Changlin Chen1, Heng Xu3, Yimin Chai2, Meidong Lang4.
Abstract
An in situ formed hydrogel was synthesized by sodium alginate and cysteine methyl ester, which turned the sodium alginate into thiolated alginate (SA-SH). SA-SH can in situ formed into hydrogel (SA-SS-SA) with a large amount of water through covalent bond in less than 20 s. The structure characterization showed that the mechanism of SA-SH gelation was thiol-disulfide transformation. The rheology and cytotoxicity experiments of SA-SS-SA hydrogel were also investigated, which indicated that SA-SS-SA hydrogel had an appropriate mechanical strength as well as an excellent biocompatibility. The SA-SS-SA hydrogel would degrade under certain conditions after a few days and its mechanism was disulfide alkaline reduction. Finally, the hemostatic property of SA-SH was tested by rat tail amputation experiment. The time to hemostasis of rat reduced from 8.26 min to 3.24 min, which proved that SA-SH had an excellent hemostatic property.Entities:
Keywords: Sodium alginate; cysteine methyl ester hydrochloride; hemostasis; in situ hydrogel; wound healing
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Year: 2016 PMID: 27485953 DOI: 10.1177/0885328216661557
Source DB: PubMed Journal: J Biomater Appl ISSN: 0885-3282 Impact factor: 2.646