In vitro degradation of silk fibroin

被引：605

作者：

Horan, RL ^{[1
]}

Antle, K ^{[1
]}

Collette, AL ^{[1
]}

Huang, YZ ^{[1
]}

Huang, J ^{[1
]}

Moreau, JE ^{[1
]}

Volloch, V ^{[1
]}

Kaplan, DL ^{[1
]}

Altman, GH ^{[1
]}

机构：

[1] Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA

来源：

BIOMATERIALS | 2005年 / 26卷 / 17期

关键词：

degradation; silk; scaffold; ligament; mechanical properties;

D O I：

10.1016/j.biomaterials.2004.09.020

中图分类号：

R318 [生物医学工程];

学科分类号：

0831 ;

摘要：

A significant need exists for long-term degradable biomaterials which can slowly and predictably transfer a load-bearing burden to developing biological tissue. In this study Bombyx mori silk fibroin yarns were incubated in 1 mg/ml Protease XIV at 37 degreesC to create an in vitro model system of proteolytic degradation. Samples were harvested at designated time points up to 12 weeks and (1) prepared for scanning electron microscopy (SEM), (2) lyophilized and weighed, (3) mechanical properties determined using a servohydraulic Instron 8511, (4) dissolved and run on a SDS-PAGE gel, and (5) characterized with Fourier transform infrared spectroscopy. Control samples were incubated in phosphate-buffered saline. Fibroin was shown to proteolytically degrade with predictable rates of change in fibroin diameter, failure strength, cycles to failure, and mass. SEM indicated increasing fragmentation of individual fibroin filaments from protease-digested samples with time of exposure to the enzyme; particulate debris was present within 7 days of incubation. Gel electrophoresis indicated a decreasing amount of the silk 25 kDa light chain and a shift in the molecular weight of the heavy chain with increasing incubation time in protease. Results support that silk is a mechanically robust biomaterial with predictable long-term degradation characteristics. (C) 2004 Elsevier Ltd. All rights reserved.

引用

页码：3385 / 3393

页数：9

共 22 条

[11] SOLVENT-INDUCED AND MECHANICAL-TREATMENT-INDUCED CONFORMATIONAL TRANSITION OF SILK FIBROINS STUDIED BY HIGH-RESOLUTION SOLID-STATE C-13 NMR-SPECTROSCOPY [J].