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基因交联纳米纤维壳聚糖垫用于引导组织再生的缝线拔出强度和体外成纤维细胞及 RAW 264.7 单核细胞生物相容性。

Suture pullout strength and in vitro fibroblast and RAW 264.7 monocyte biocompatibility of genipin crosslinked nanofibrous chitosan mats for guided tissue regeneration.

机构信息

Department of Biomedical Engineering, University of Memphis, Memphis, Tennessee.

出版信息

J Biomed Mater Res A. 2012 Nov;100(11):2890-6. doi: 10.1002/jbm.a.34224. Epub 2012 Jun 14.

DOI:10.1002/jbm.a.34224
PMID:22696151
Abstract

Guided tissue regeneration (GTR) is a surgical technique used to direct the formation of bone in the graft space by protecting it with a barrier membrane used to exclude soft tissues during healing. Chitosan has been advocated for GTR applications because of its biocompatibility, degradability, wound healing, and osteogenic properties. In this study, electrospun chitosan membranes, crosslinked with 5 mM or 10 mM geinipin, a natural crosslinker extracted from the gardenia plant, were evaluated for suture pullout strength, crystallinity, and cytocompatibility with normal human dermal fibroblast and TIB 71™ RAW 264.7 monocyte cells. Ultimate suture pullout strength was significantly lower (51-67%) than that of commercially available collagen membranes. Crystallinity of the electrospun chitosan mats decreased upon crosslinking by 14-17% (p = 0.013). The molecular weight of the chitosan polymer was decreased by 75% during the electrospinning process. Uncrosslinked and genipin-crosslinked chitosan mats were cytocompatible and supported fibroblast cell proliferation for 9 days. Uncrosslinked and genipin-crosslinked membranes did not activate monocytes to produce nitric oxide (NO) in vitro in the absence of lipopolysaccharide (LPS). Finally, chitosan membranes inhibited LPS-induced NO production of RAW 264.7 cells by 59-67% as compared to tissue culture plastic and collagen membrane. Improvements are needed in the tear strength of electrospun chitosan membranes for clinical application.

摘要

引导组织再生(GTR)是一种通过使用屏障膜保护移植物空间中的骨形成的外科技术,该屏障膜用于在愈合过程中排除软组织。壳聚糖因其生物相容性、可降解性、伤口愈合和成骨特性而被提倡用于 GTR 应用。在这项研究中,用 5 mM 或 10 mM 京尼平交联的静电纺丝壳聚糖膜,京尼平是从栀子植物中提取的天然交联剂,用于评估缝线拔出强度、结晶度以及与正常人类真皮成纤维细胞和 TIB 71™ RAW 264.7 单核细胞的细胞相容性。最终的缝线拔出强度明显低于(51-67%)市售胶原膜。静电纺丝壳聚糖垫的结晶度通过交联降低了 14-17%(p = 0.013)。壳聚糖聚合物的分子量在静电纺丝过程中降低了 75%。未交联和京尼平交联的壳聚糖垫细胞相容性良好,并支持成纤维细胞增殖 9 天。在没有脂多糖(LPS)的情况下,未交联和京尼平交联的膜不会激活单核细胞产生一氧化氮(NO)。最后,与组织培养塑料和胶原膜相比,壳聚糖膜抑制 LPS 诱导的 RAW 264.7 细胞产生的 NO 增加了 59-67%。需要提高静电纺丝壳聚糖膜的撕裂强度,以满足临床应用的要求。

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