Niu Xufeng, Feng Qingling, Wang Mingbo, Guo Xiaodong, Zheng Qixin
State Key Laboratory of New Ceramics and Fine Processing, Department of Materials Science and Engineering, Tsinghua University, Beijing, People's Republic of China.
J Control Release. 2009 Mar 4;134(2):111-7. doi: 10.1016/j.jconrel.2008.11.020. Epub 2008 Dec 3.
It is advantageous to incorporate controlled growth factor delivery into tissue engineering strategies. The purpose of the present study was to develop a novel tissue engineering scaffold with the capability of controlled releasing BMP-2-derived synthetic peptide. Porous nano-hydroxyapatite/collagen/poly(L-lactic acid)/chitosan microspheres (nHAC/PLLA/CMs) composite scaffolds containing different quantities of chitosan microspheres (CMs) were prepared by a thermally induced phase separation method. Dioxane was used as the solvent for PLLA. Introduction of less than 30% of CMs (on PLLA weight basis) did not remarkably affect the morphology and porosity of the nHAC/PLLA/CMs scaffolds. However, as the microspheres contents increased to 50%, the porosity of the composite decreased rapidly. The compressive modulus of the composite scaffolds increased from 15.4 to 25.5 MPa, while the compressive strength increased from 1.42 to 1.63 MPa as the microspheres contents increased from 0% to 50%. The hydrolytic degradation and synthetic peptide release kinetics in vitro were investigated by incubation in phosphate buffered saline solution (pH 7.4). The results indicated that the degradation rate of the scaffolds was increased with the enhancement of CMs dosage. The synthetic peptide was released in a temporally controlled manner, depending on the degradation of both incorporated chitosan microspheres and PLLA matrix. In vitro bioactivity assay revealed that the encapsulated synthetic peptide was biologically active as evidenced by stimulation of rabbit marrow mesenchymal stem cells (MSCs) alkaline phosphatase (ALP) activity. The successful microspheres-scaffold system offers a new delivery method of growth factors and a novel scaffold design for bone regeneration.
将可控生长因子递送纳入组织工程策略具有优势。本研究的目的是开发一种具有可控释放BMP - 2衍生合成肽能力的新型组织工程支架。通过热致相分离法制备了含有不同数量壳聚糖微球(CMs)的多孔纳米羟基磷灰石/胶原蛋白/聚(L - 乳酸)/壳聚糖微球(nHAC/PLLA/CMs)复合支架。二氧六环用作聚乳酸(PLLA)的溶剂。引入少于30%(基于PLLA重量)的CMs对nHAC/PLLA/CMs支架的形态和孔隙率没有显著影响。然而,当微球含量增加到50%时,复合材料的孔隙率迅速下降。随着微球含量从0%增加到50%,复合支架的压缩模量从15.4 MPa增加到25.5 MPa,而压缩强度从1.42 MPa增加到1.63 MPa。通过在磷酸盐缓冲盐溶液(pH 7.4)中孵育来研究体外水解降解和合成肽释放动力学。结果表明,支架的降解速率随着CMs剂量的增加而增加。合成肽以时间可控的方式释放,这取决于所含壳聚糖微球和PLLA基质的降解。体外生物活性测定表明,包封的合成肽具有生物活性,兔骨髓间充质干细胞(MSCs)碱性磷酸酶(ALP)活性的刺激证明了这一点。成功的微球 - 支架系统为生长因子提供了一种新的递送方法,并为骨再生提供了一种新型支架设计。