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用于潜在药物载体系统的胶原微纤维和纳米纤维的生产。

Production of collagen micro- and nanofibers for potential drug-carrier systems.

作者信息

Aras Onur, Kazanci Murat

机构信息

a Department of Biophysics , School of Medicine, Bahcesehir University , Istanbul , Turkey.

出版信息

J Enzyme Inhib Med Chem. 2015 Dec;30(6):1013-6. doi: 10.3109/14756366.2014.976567. Epub 2015 Mar 6.

Abstract

Two different nano- and micro-collagen fiber production methods are introduced and discussed. First one is the electrospinning method, that is very common technique to produce nanofibers from different polymeric solutions and recently collagen solutions are employed to produce nanofibers for different biomedical applications. This technique is extremely versatile method to produce nanofibers in a relatively short time, easy to control the fiber diameter and orientation with small pore sizes and a high surface area. The second method is self-assembly of collagen micro-fibers by co-extrusion method. The collagen fibers are obtained without any cross-linker, by using mainly ionic interactions. We demonstrated that self-assembled collagen fibers have well preserved their native structure (0.90 PP-II fraction), when compared with electrospun collagen fibers (0.38 PP-II fraction). However, it was only possible to produce collagen fibers with nanodimensions by using electrospinning method.

摘要

介绍并讨论了两种不同的纳米和微胶原纤维生产方法。第一种是静电纺丝法,这是一种从不同聚合物溶液中生产纳米纤维的非常常见的技术,最近胶原溶液被用于生产用于不同生物医学应用的纳米纤维。该技术是一种极其通用的方法,能够在相对较短的时间内生产纳米纤维,易于控制纤维直径和取向,具有小孔径和高表面积。第二种方法是通过共挤出法自组装胶原微纤维。通过主要利用离子相互作用,无需任何交联剂即可获得胶原纤维。我们证明,与静电纺丝胶原纤维(0.38 PP-II 分数)相比,自组装胶原纤维很好地保留了其天然结构(0.90 PP-II 分数)。然而,只有通过静电纺丝法才能生产出纳米尺寸的胶原纤维。

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