Li Ting-Ting, Ebert Katrin, Vogel Jürgen, Groth Thomas
Department Pharmaceutics and Biopharmaceutics, Biomedical Materials Group, Martin Luther University Halle-Wittenberg, Institute of Pharmacy, Heinrich-Damerow-Strasse 4, Halle (Saale), 06120, Germany.
GKSS Research Centre Geesthacht GmbH, Institute of Polymer Research, Max-Planck-Str.1, Geesthacht, 21502, Germany.
Prog Biomater. 2013 Nov 14;2(1):13. doi: 10.1186/2194-0517-2-13.
The biocompatibility and osteogenic potential of four fibrous scaffolds prepared by electrospinning of poly(ε-caprolactone) (PCL) was studied with MG-63 osteoblast cells. Two different kinds of scaffolds were obtained by adjustment of spinning conditions, which were characterized as nano- or microfibrous. In addition of one nanofibrous, scaffold was made more hydrophilic by blending PCL with Pluronics F 68. Scaffolds were characterized by scanning electron microscopy and water contact angle measurements. Morphology and growth of MG63 cells seeded on the different scaffolds were investigated by confocal laser scanning microscopy after vital staining with fluorescein diacetate and by colorimetric assays. It was found that scaffolds composed of microfibres stipulated better growth conditions for osteoblasts probably by providing a real three-dimensional culture substratum, while nanofibre scaffolds restricted cell growth predominantly to surface regions. Osteogenic activity of cells was determined by alkaline phosphatase (ALP) and o-cresolphthalein complexone assay. It was observed that osteogenic activity of cells cultured in microfibre scaffolds was significantly higher than in nanofibre scaffolds regarding ALP activity. Overall, one can conclude that nanofibre scaffold provides better conditions for initial attachment of cells but does not provide advantages in terms of scaffold colonization and support of osteogenic activity compared to scaffolds prepared from microfibres.
利用MG - 63成骨细胞研究了通过静电纺丝聚(ε-己内酯)(PCL)制备的四种纤维支架的生物相容性和成骨潜力。通过调整纺丝条件获得了两种不同类型的支架,其特征为纳米纤维或微纤维。除了一种纳米纤维支架外,通过将PCL与普朗尼克F68混合使支架具有更高的亲水性。通过扫描电子显微镜和水接触角测量对支架进行表征。在用荧光素二乙酸酯进行活细胞染色后,通过共聚焦激光扫描显微镜和比色法研究接种在不同支架上的MG63细胞的形态和生长情况。发现由微纤维组成的支架可能通过提供真实的三维培养基质为成骨细胞规定了更好的生长条件,而纳米纤维支架主要将细胞生长限制在表面区域。通过碱性磷酸酶(ALP)和邻甲酚酞络合酮测定法测定细胞的成骨活性。观察到就ALP活性而言,在微纤维支架中培养的细胞的成骨活性明显高于纳米纤维支架中的细胞。总体而言,可以得出结论,与由微纤维制备的支架相比,纳米纤维支架为细胞的初始附着提供了更好的条件,但在支架定植和成骨活性支持方面没有优势。