Catledge S A, Clem W C, Shrikishen N, Chowdhury S, Stanishevsky A V, Koopman M, Vohra Y K
Department of Physics, University of Alabama at Birmingham, Birmingham, AL 35294-1170, USA.
Biomed Mater. 2007 Jun;2(2):142-50. doi: 10.1088/1748-6041/2/2/013. Epub 2007 May 8.
A nanofibrous triphasic scaffold was electrospun from a mixture of polycaprolactone (PCL), type-I collagen and hydroxyapatite nanoparticles (nano-HA) with a mixture dry weight ratio of 50/30/20, respectively. Scaffolds were characterized by evaluating fiber morphology and chemical composition, dispersion of HA particles and nanoindentation. Scanning electron microscopy revealed fibers with an average diameter of 180 +/- 50 nm, which coincides well with the collagen fiber bundle diameter characteristic of the native extracellular matrix of bone. The triphasic fibers, stained with calcein and imaged with confocal microscopy, show a uniform dispersion of apatite particles throughout their length with minor agglomeration. Scaffold fibers of triphasic (50/30/20), collagen/nano-HA (80/20), PCL/nano-HA (80/20), pure PCL and pure collagen were each pressure consolidated into non-porous pellets for evaluation by transmission electron microscopy and nanoindentation. While the majority of apatite particles are uniformly dispersed having an average size of 30 nm, agglomerated particles as large as a few microns are sparsely distributed. Nanoindentation of the pressure-consolidated scaffolds showed a range of Young's modulus (0.50-3.9 GPa), with increasing average modulus in the order of (PCL < PCL/nano-HA < collagen < triphasic < collagen/nano-HA). The modulus data emphasize the importance of collagen and its interaction with other components in affecting mechanical properties of osteoconductive scaffolds.
一种纳米纤维三相支架由聚己内酯(PCL)、I型胶原蛋白和羟基磷灰石纳米颗粒(纳米HA)的混合物通过静电纺丝制成,其混合物干重比分别为50/30/20。通过评估纤维形态和化学成分、HA颗粒的分散情况以及纳米压痕来对支架进行表征。扫描电子显微镜显示纤维的平均直径为180±50纳米,这与骨天然细胞外基质特有的胶原纤维束直径非常吻合。用钙黄绿素染色并用共聚焦显微镜成像的三相纤维显示磷灰石颗粒在其整个长度上均匀分散,仅有少量团聚。将三相(50/30/20)、胶原蛋白/纳米HA(80/20)、PCL/纳米HA(80/20)、纯PCL和纯胶原蛋白的支架纤维分别进行压力固结制成无孔颗粒,用于透射电子显微镜和纳米压痕评估。虽然大多数磷灰石颗粒均匀分散,平均尺寸为30纳米,但也有少数几微米大小的团聚颗粒稀疏分布。压力固结支架的纳米压痕显示杨氏模量范围为(0.50 - 3.9吉帕),平均模量按(PCL < PCL/纳米HA < 胶原蛋白 < 三相 < 胶原蛋白/纳米HA)的顺序增加。模量数据强调了胶原蛋白及其与其他成分的相互作用在影响骨传导性支架力学性能方面的重要性。