A Biomimetic Tubular Scaffold With Spatially Designed Nanofibers of Protein/PDS® Bio-Blends

被引:62
作者
Thomas, Vinoy [1 ]
Zhang, Xing [2 ]
Vohra, Yogesh K. [1 ]
机构
[1] Univ Alabama, Dept Phys, CNMB, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Biomed Engn, Birmingham, AL 35294 USA
基金
美国国家科学基金会;
关键词
nanofibers; polydioxanone; electrospinning; vascular grafts; biodegradation; IN-VITRO DEGRADATION; HYDROLYTIC DEGRADATION; ELASTIN BLENDS; BIOMEDICAL APPLICATIONS; VASCULAR GRAFT; FABRICATION; POLY(P-DIOXANONE); POLYDIOXANONE; COLLAGEN; MORPHOLOGY;
D O I
10.1002/bit.22467
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Electospuin tubular conduit (4mm inner diameter) based on blends of polydioxanone (PDS II (R)) and proteins such as gelatin and elastin having a spatially designed trilayer structure was prepared for arterial scaffolds. SEM analysis of scaffolds showed random nanofibrous morphology and wll-interconnected pore network. Due to protein blending, the fiber diameter was reduced from 800-950 nm range to 300-500 nm range. Fourier transofrm infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) results confirmed the blended composition and crystallinity of fibers. Pure PDS scaffold under hydrated, state exhibited a tensile strength of 5.61 +/- 0.42 MPa and a modulus of 17.11 +/- 1.13 MPa with a failure strain of 216.7 +/- 1.3%. The blending of PDS with elastin and gelatin has decreased the tensile properties. A trilayer tubular scaffold was fabricated by sequential electrospinning of blends of elastin/gelatin, PDS/elastin/gelatin, and PDS/gelatin (EG/PEG/PG) to mimic the complex matrix structure of native arteries. Under hydrated state the trilayer conduit exhibited tensile properties (tensile strength of 1.77 +/- 0.2 MPa and elastic modulus of 5.74 +/- 0.2 MPa with a failure strain of 75.08 +/- 10%) comparable to those of native arteries. In vitro degradation studies for up to 30 days showed about 40% mass loss and increase in crystallinity due to the removal of proteins and "cleavage-induced crystallization" of PDS. Biotechnol. Bioeng. 2009;104: 1025-1033. (C) 2009 Wiley Periodicals, Inc.
引用
收藏
页码:1025 / 1033
页数:9
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