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γ-聚谷氨酸/壳聚糖复合组织工程基质的制备

Preparation of gamma-PGA/chitosan composite tissue engineering matrices.

作者信息

Hsieh Chien-Yang, Tsai Sung-Pei, Wang Da-Ming, Chang Yaw-Nan, Hsieh Hsyue-Jen

机构信息

Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan, ROC.

出版信息

Biomaterials. 2005 Oct;26(28):5617-23. doi: 10.1016/j.biomaterials.2005.02.012. Epub 2005 Apr 7.

Abstract

Gamma-poly(glutamic acid) (gamma-PGA), a hydrophilic and biodegradable polymer, was chosen to modify chitosan matrices to produce a gamma-PGA/chitosan composite biomaterial. Three types of both dense and porous composite matrices containing different amounts of gamma-PGA were fabricated. Chitosan and gamma-PGA matrices were also prepared as controls. Fluorescence staining indicated that chitosan and gamma-PGA were evenly distributed in the composite matrices. SEM micrographs showed that an interconnected porous structure with a pore size of 30-100 microm was present in all porous matrices except the gamma-PGA ones. By increasing the percentage of gamma-PGA from 0% to 20%, the swelling ratio of the matrices was enhanced from 1.6 to 3.2. Similarly, the contact angle of the matrices decreased from 113 degrees to 94 degrees . These data suggested that the surface hydrophilicity, water absorption rate, and swelling ratio were improved by adding gamma-PGA to the matrices. Additionally, the mechanical strength of the porous gamma-PGA/chitosan matrices was about 25-50%, higher than that of the unmodified chitosan matrices. The composite matrices were also examined and found to be an appropriate environment for cell attachment and proliferation. The cell density on the 20% gamma-PGA-modified matrices was almost triple that on the unmodified chitosan matrices on day 5. In summary, the gamma-PGA/chitosan composite matrices, due to their better hydrophilic, cytocompatible, and mechanical properties, are very promising biomaterials for tissue engineering applications.

摘要

γ-聚谷氨酸(γ-PGA)是一种亲水性可生物降解聚合物,被用于修饰壳聚糖基质以制备γ-PGA/壳聚糖复合生物材料。制备了三种含有不同量γ-PGA的致密和多孔复合基质。壳聚糖和γ-PGA基质也作为对照制备。荧光染色表明壳聚糖和γ-PGA在复合基质中均匀分布。扫描电子显微镜图像显示,除γ-PGA基质外,所有多孔基质中均存在孔径为30-100微米的相互连通的多孔结构。通过将γ-PGA的百分比从0%增加到20%,基质的溶胀率从1.6提高到3.2。同样,基质的接触角从113度降低到94度。这些数据表明,通过向基质中添加γ-PGA,表面亲水性、吸水率和溶胀率得到了改善。此外,多孔γ-PGA/壳聚糖基质的机械强度比未改性的壳聚糖基质高约25-50%。还对复合基质进行了检查,发现其是细胞附着和增殖的适宜环境。在第5天,20%γ-PGA改性基质上的细胞密度几乎是未改性壳聚糖基质上的三倍。总之,γ-PGA/壳聚糖复合基质由于其更好的亲水性、细胞相容性和机械性能,是用于组织工程应用的非常有前途的生物材料。

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