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纳米羟基磷灰石/壳聚糖/罗非鱼皮肽水凝胶的制备及其烧伤创面治疗。

Preparation of nano-hydroxyapatite/chitosan/tilapia skin peptides hydrogels and its burn wound treatment.

机构信息

Marine Biomedical Research Institute, the Key Lab of Zhanjiang for R&D Marine Microbial Resources in the Beibu Gulf Rim, Guangdong Medical University, Zhanjiang 524023, China; Southern Marine Science and Engineering Guangdong Laboratory (Zhanjiang), Zhanjiang 524023, China; The Marine Biomedical Research Institute of Guangdong Zhanjiang, Zhanjiang 524023, China.

School of Chemistry and Environmental Science, Guangdong Ocean University, Zhanjiang 524088, China.

出版信息

Int J Biol Macromol. 2021 Jun 30;181:369-377. doi: 10.1016/j.ijbiomac.2021.03.085. Epub 2021 Mar 15.

Abstract

There is an urgent need for wound dressings to treat partial-thickness burns. Hydrogels are a promising material that can maintain hydration to promote necrotic tissue removal. Tilapia peptides (TP) and hydroxyapatite (HA) were incorporated into chitosan system to prepare new types of hydrogels. The hydrogels were cross-linking by tannin (TA), which were developed to promote rapid wound healing in a New Zealand rabbit partial-thickness burn model. Nanohydroxyapatite (NHA) was synthesized by coprecipitation method, which made hydrogels have a highly porous structure comprised of interconnected pores, excellent water absorption and low hemolysis. Besides, the hydrogels showed excellent antimicrobial activities against both Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), as well as the cytocompatibility on endothelial cells. Moreover, the hydrogels promoted epithelial and dermal regeneration, reduce the expression of TNF-α and IL-6 and promote the skin regeneration by enhancing expression of collagen, STAT3, and VEGF.

摘要

目前急需用于治疗部分厚度烧伤的伤口敷料。水凝胶是一种很有前途的材料,可以保持水分以促进坏死组织的去除。将罗非鱼肽(TP)和羟基磷灰石(HA)掺入壳聚糖体系中,以制备新型水凝胶。水凝胶通过单宁(TA)交联,旨在促进新西兰兔部分厚度烧伤模型的快速伤口愈合。纳米羟基磷灰石(NHA)通过共沉淀法合成,使水凝胶具有由相互连接的孔组成的高度多孔结构,具有出色的吸水性和低溶血率。此外,水凝胶对大肠杆菌(E. coli)和金黄色葡萄球菌(S. aureus)均表现出优异的抗菌活性,并且对内皮细胞具有良好的细胞相容性。而且,水凝胶可促进上皮和真皮再生,通过增强胶原、STAT3 和 VEGF 的表达来减少 TNF-α 和 IL-6 的表达并促进皮肤再生。

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