多孔性
材料科学
PLGA公司
脚手架
生物医学工程
乙醇酸
抗压强度
化学工程
组织工程
复合材料
微球
乳酸
纳米技术
纳米颗粒
生物
医学
工程类
遗传学
细菌
作者
Omar Qutachi,Jolanda Rita Vetsch,Daniel Gill,Helen C. Cox,David J. Scurr,Sandra Hofmann,Ralph Müller,Robin A. Quirk,Kevin M. Shakesheff,Cheryl V. Rahman
标识
DOI:10.1016/j.actbio.2014.08.015
摘要
Injectable scaffolds are of interest in the field of regenerative medicine because of their minimally invasive mode of delivery. For tissue repair applications, it is essential that such scaffolds have the mechanical properties, porosity and pore diameter to support the formation of new tissue. In the current study, porous poly(dl-lactic acid-co-glycolic acid) (PLGA) microspheres were fabricated with an average size of 84±24μm for use as injectable cell carriers. Treatment with ethanolic sodium hydroxide for 2min was observed to increase surface porosity without causing the microsphere structure to disintegrate. This surface treatment also enabled the microspheres to fuse together at 37°C to form scaffold structures. The average compressive strength of the scaffolds after 24h at 37°C was 0.9±0.1MPa, and the average Young's modulus was 9.4±1.2MPa. Scaffold porosity levels were 81.6% on average, with a mean pore diameter of 54±38μm. This study demonstrates a method for fabricating porous PLGA microspheres that form solid porous scaffolds at body temperature, creating an injectable system capable of supporting NIH-3T3 cell attachment and proliferation in vitro.
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