Qasim Saad B, Najeeb Shariq, Delaine-Smith Robin M, Rawlinson Andrew, Ur Rehman Ihtesham
Materials Science and Engineering Department, Kroto Research Institute, University of Sheffield, Sheffield S3 7HQ, United Kingdom.
School of Clinical Dentistry, University of Sheffield, University of Sheffield, Sheffield S10 2SZ, United Kingdom.
Dent Mater. 2017 Jan;33(1):71-83. doi: 10.1016/j.dental.2016.10.003. Epub 2016 Nov 11.
The regeneration of periodontal tissues lost as a consequence of destructive periodontal disease remains a challenge for clinicians. Guided tissue regeneration (GTR) has emerged as the most widely practiced regenerative procedure. Aim of this study was to electrospin chitosan (CH) membranes with a low or high degree of fiber orientation and examines their suitability for use as a surface layer in GTR membranes, which can ease integration with the periodontal tissue by controlling the direction of cell growth.
A solution of CH-doped with polyethylene oxide (PEO) (ratio 95:5) was prepared for electrospinning. Characterization was performed for biophysiochemical and mechanical properties by means of scanning electron microscopy (SEM), Fourier Transform Infrared (FTIR) spectroscopy, swelling ratio, tensile testing and monitoring degradation using pH analysis, weight profile, ultraviolet-visible (UV-vis) spectroscopy and FTIR analysis. Obtained fibers were also assessed for viability and matrix deposition using human osteosarcoma (MG63) and human embryonic stem cell-derived mesenchymal progenitor (hES-MP) cells.
Random and aligned CH fibers were obtained. FTIR analysis showed neat CH spectral profile before and after electrospinning. Electropsun mats were conducive to cellular attachment and viability increased with time. The fibers supported matrix deposition by hES-MPs. Histological sections showed cellular infiltration as well.
The surface layer would act as seal to prevent junctional epithelium from falling into the defect site and hence maintain space for bone regeneration.
因破坏性牙周疾病而丧失的牙周组织再生仍是临床医生面临的一项挑战。引导组织再生术(GTR)已成为应用最广泛的再生程序。本研究的目的是静电纺丝制备纤维取向度低或高的壳聚糖(CH)膜,并考察其作为GTR膜表层的适用性,通过控制细胞生长方向,该表层可促进与牙周组织的整合。
制备掺有聚环氧乙烷(PEO)(比例95:5)的CH溶液用于静电纺丝。通过扫描电子显微镜(SEM)、傅里叶变换红外(FTIR)光谱、溶胀率、拉伸试验以及使用pH分析、重量变化、紫外可见(UV-vis)光谱和FTIR分析监测降解情况,对生物物理化学和机械性能进行表征。还使用人骨肉瘤(MG63)细胞和人胚胎干细胞来源的间充质祖细胞(hES-MP)评估所获得纤维的活力和基质沉积情况。
获得了随机排列和取向排列的CH纤维。FTIR分析显示静电纺丝前后CH光谱特征良好。静电纺丝垫有利于细胞附着,且活力随时间增加。这些纤维支持hES-MP细胞的基质沉积。组织学切片也显示有细胞浸润。
表层可起到密封作用,防止结合上皮落入缺损部位,从而为骨再生保留空间。