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首页> 外文期刊>Materials science & engineering >Macroporous and nanofibrous poly(lactide-co-glycolide) (50/50) scaffolds via phase separation combined with particle-leaching
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Macroporous and nanofibrous poly(lactide-co-glycolide) (50/50) scaffolds via phase separation combined with particle-leaching

机译:大孔和纳米纤维聚(丙交酯-共-乙交酯)(50/50)支架通过相分离结合颗粒浸出

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摘要

Poly(lactide-co-glycolide) (PLGA) copolymers are the most prevalent materials for tissue engineering applications. To mimic the real microenvironment of extracellular matrix (ECM) for cell growth, nanofibrous PLGA scaffolds are preferred. PLGA5050 (in which the molar ratio of lactidyl to glycolidyl units is 50:50), which is an utterly amorphous polymer, was first reported to be made into nanofibrous networks (fiber diameter around 500 nm) using phase separation from PLGA5050/THF solutions in this study. The concentration of polymeric solution had significant effects on fiber diameter and unit length. Nonsolvent (e.g. H_2O) was unnecessary to form the PLGA5050 gel, which was critical to nanofibrosis, as if the environmental temperature for gelation occurrence was low enough (-70℃). The physical crosslinks to stabilize the PLGA5050/THF gel were believed to be GA segments along the backbone owing to their inferior solubility in THF. The addition of H_2O would cause adverse effects of liquid-liquid phase separation and nanofibrosis failure owing to the hy-drophilicity of glycolidyl units. Associating with the phase separation method, particle-leaching technique was applied to fabricate three-dimensional scaffolds with macroporous and nanofibrous structures. To ensure the occurrence of nanofibrosis on macropore walls, the temperature of salt particles should be best lowed to - 70℃ beforehand. Accordingly, scaffolds prepared under varied parameters exhibited different nanofiber and pore morphologies, which affected the pore size, porosity, specific surface area, water contact angle and protein adsorption ability etc. The preliminary cell (MC3T3-E1) culture confirmed the cell ingrowth into the macroporous and nanofibrous PLGA5050 scaffolds in comparison with the solely nanofibrous matrixes. This kind of bi-scaled three dimensional matrixes can be superior candidate scaffolds for tissue engineering applications.
机译:聚(丙交酯-共-乙交酯)(PLGA)共聚物是用于组织工程应用的最流行的材料。为了模拟细胞外基质(ECM)的真实微环境以促进细胞生长,首选纳米纤维PLGA支架。首先报道了PLGA5050(其中的丙二酰基与羟丙基的摩尔比为50:50),这是一种完全无定形的聚合物,它是利用PLGA5050 / THF溶液中的相分离法制成纳米纤维网络(纤维直径约为500 nm)。这项研究。聚合物溶液的浓度对纤维直径和单位长度具有显着影响。不需要非溶剂(例如H_2O)即可形成PLGA5050凝胶,该凝胶对于纳米纤维化至关重要,仿佛发生凝胶作用的环境温度足够低(-70℃)。稳定PLGA5050 / THF凝胶的物理交联被认为是骨架上的GA链段,因为它们在THF中的溶解性较差。由于缩水甘油基单元的亲水性,H_2O的添加将引起液相-液相分离和纳米纤维化失败的不利影响。结合相分离法,应用颗粒浸出技术制备具有大孔和纳米纤维结构的三维支架。为了确保在大孔壁上发生纳米纤维化,应事先将盐粒的温度降低至-70℃。因此,在不同参数下制备的支架表现出不同的纳米纤维和孔形态,从而影响孔的大小,孔隙率,比表面积,水接触角和蛋白质吸附能力等。初步细胞(MC3T3-E1)培养证实细胞向内生长。与仅纳米纤维基质相比,大孔和纳米纤维PLGA5050支架。这种双尺度的三维矩阵可以是组织工程应用的优秀候选支架。

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  • 来源
    《Materials science & engineering》 |2012年第6期|p.1407-1414|共8页
  • 作者单位

    Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029, PR China;

    Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029, PR China;

    Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029, PR China;

    Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029, PR China;

    School and Hospital of Stomatology, Perking University, Beijing 100081. PR China;

    Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029, PR China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    poly(lactide-co-glycolide); phase separation; particle-leaching; macroporous; nanofibrous;

    机译:聚(丙交酯-共-乙交酯);相分离;颗粒浸出大孔纳米纤维;

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