Goonoo N, Bhaw-Luximon A, Rodriguez I A, Wesner D, Schönherr H, Bowlin G L, Jhurry D
ANDI Centre of Excellence for Biomedical and Biomaterials Research, University of Mauritius, MSIRI Building, Réduit, Mauritius.
J Mater Chem B. 2015 Jan 28;3(4):673-687. doi: 10.1039/c4tb01350f. Epub 2014 Dec 1.
The aim of this paper is to investigate the physico-chemical properties, degradation behaviour and cellular response of electrospun fibre-scaffolds of semi-crystalline PCL, PLLA and PDX blended with amorphous poly(methyl dioxanone) (PMeDX). Electrospun PCL/PMeDX and PLLA/PMeDX blend mats in varying weight ratios of the two components were fabricated and their overall performance was compared with similar composition PDX/PMeDX scaffolds. DSC analysis showed almost no change in crystallization temperature of PCL with increasing PMeDX content and TGA showed a different degradation profile as PMeDX content increased. The appearance of two crystallization peaks for PLLA/PMeDX blends suggested stereocomplex formation. As noted from AFM images, addition of PMeDX caused a change in the width of the lamellae from 14.8 ± 2.9 nm in 100/0 mat to 32.0 ± 11.5 nm in 85/15 mat. Moreover, PCL/PMeDX blend mats show a significant drop in Young's modulus for 93/7, 90/10 and 85/15 compositions compared to 100/0 and 98/2. On the other hand, no clear trend in mechanical properties was observed for espun PLLA/PMeDX mats with increasing PMeDX content. Based on these analyses, it was concluded that PCL and PMeDX were immiscible while miscible blends were obtained with PLLA and PMeDX. Initial degradation of electrospun mats over a period of 5 weeks appears to occur via a surface erosion mechanism. In vitro cell culture studies using HDFs showed that the scaffolds were bioactive and a greater density of viable cells was noted on electrospun PCL/PMeDX and PLLA/PMeDX scaffolds compared to PCL and PLLA mats respectively. HDFs infiltrated through the entire thickness of espun 85/15 PLLA/PMeDX scaffold due to a combination of factors including morphology, porosity, surface characteristics and mechanical properties.
本文旨在研究半结晶聚己内酯(PCL)、聚乳酸(PLLA)和聚二氧杂环己酮(PDX)与无定形聚(甲基二氧杂环己酮)(PMeDX)共混的电纺纤维支架的物理化学性质、降解行为和细胞反应。制备了两种组分不同重量比的电纺PCL/PMeDX和PLLA/PMeDX共混垫,并将它们的整体性能与类似组成的PDX/PMeDX支架进行了比较。差示扫描量热法(DSC)分析表明,随着PMeDX含量的增加,PCL的结晶温度几乎没有变化,热重分析(TGA)表明随着PMeDX含量的增加,降解曲线不同。PLLA/PMeDX共混物出现两个结晶峰表明形成了立体复合物。从原子力显微镜(AFM)图像可以看出,添加PMeDX导致片层宽度从100/0垫中的14.8±2.9纳米变为85/15垫中的32.0±11.5纳米。此外,与100/0和98/2相比,PCL/PMeDX共混垫在93/7、90/10和85/15组成时杨氏模量显著下降。另一方面,随着PMeDX含量的增加,电纺PLLA/PMeDX垫的力学性能没有明显趋势。基于这些分析,得出结论:PCL和PMeDX不相容,而PLLA和PMeDX形成了互溶共混物。电纺垫在5周内的初始降解似乎是通过表面侵蚀机制发生的。使用人皮肤成纤维细胞(HDFs)进行的体外细胞培养研究表明,支架具有生物活性,与PCL和PLLA垫相比,在电纺PCL/PMeDX和PLLA/PMeDX支架上分别观察到更高密度的活细胞。由于包括形态、孔隙率、表面特性和力学性能在内的多种因素的综合作用,HDFs渗透到了电纺85/15 PLLA/PMeDX支架的整个厚度。