PLGA公司
纤维蛋白
戊二醛
复合数
材料科学
纤维蛋白原
化学工程
生物医学工程
凝血酶
组织工程
高分子化学
复合材料
化学
色谱法
纳米技术
血小板
生物化学
纳米颗粒
医学
工程类
免疫学
生物
作者
Haiguang Zhao,Lie Ma,Changyou Gao,Jiacong Shen
摘要
Abstract A composite scaffold of poly( L ‐lactic‐ co ‐glycolic acid) (PLGA) microspheres and fibrin gel was fabricated by blending fibrinogen‐immobilized PLGA microspheres with fibrinogen and thrombin solution. The PLGA microspheres with a size of 70 ∼ 100 μm were aminolyzed in a hexanediamine/ n ‐propanol solution to introduce free amino groups on their surface. The fibrinogen immobilization was achieved by glutaraldehyde coupling. When the NH 2 content on the microsphere surface was increased from ∼2 × 10 −8 mol/mg to ∼4 × 10 −8 mol/mg, the fibrinogen amount was correspondingly increased from ∼35 μg/mg to ∼70 μg/mg. Measured by UV‐VIS spectroscopy, the clotting time of the composite was less influenced by the microsphere amount, but mainly controlled by the thrombin concentration. When the thrombin concentration was higher than 15 U/mL, the gelation could be finished within 1 min and yielded a composite with evenly suspended and distributed PLGA microspheres. Blending with the microspheres could significantly improve the elastic modulus of the hydrogel as well, whereas less influence on the chondrocyte proliferation and extracellular matrix production. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2009
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