首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Controlled formation of polylysinized inner pores in injectable microspheres of low molecular weight poly(lactide-co-glycolide) designed for efficient loading of therapeutic cells
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Controlled formation of polylysinized inner pores in injectable microspheres of low molecular weight poly(lactide-co-glycolide) designed for efficient loading of therapeutic cells

机译:为有效装载治疗性细胞而设计的低分子量聚丙交酯-乙交酯共聚物可注射微球中多聚酶化内孔的受控形成

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This study aimed to develop porous microspheres with a suitable porous structure and mechanical property for cell delivery using a comparatively low molecular weight (MW) poly(lactide-co-glycolide) (PLGA) having a weak mechanical strength and fast degradation rate, which could be potentially used for treatment of corneal endothelial diseases. Porous microspheres of 30?kDa PLGA with different pore sizes were prepared by varying preparation conditions, and the microspheres with mean pore diameters approximately 0.5, 1, 2 and 3 times that of a single green fluorescent protein-expressing human embryonic kidney 293 cell, used as a model cell, were chosen for cell loading study. The microspheres with an average pore diameter two times greater than that of the single cell were found to be the most appropriate for efficient cell loading in the inner pore spaces, along with demonstrating a good mechanical property, injectability and biodegradability. To maximize the cell loading amount in the microspheres, the cell adhesive property of the microspheres and cell loading conditions were optimized, leading to approximately 4.2 times increase in the cell loading amount. The porous microspheres designed using the low MW PLGA hold promise as a delivery system of corneal endothelial cells for regeneration of the corneal endothelium.
机译:这项研究旨在使用机械强度较弱且降解速度较快的相对较低分子量(MW)的聚丙交酯乙交酯共聚物(PLGA),开发出具有合适的多孔结构和机械特性的多孔微球,以用于细胞递送被潜在地用于治疗角膜内皮疾病。通过改变制备条件,制备了具有不同孔径的30?kDa PLGA多孔微球,使用的微球的平均孔径约为表达单个绿色荧光蛋白的人类胚胎肾293细胞的平均孔径的0.5、1、2和3倍。作为模型细胞,选择用于细胞负载研究。发现平均孔径比单个细胞大两倍的微球最适合内部孔空间中的有效细胞加载,并显示出良好的机械性能,可注射性和生物降解性。为了使微球中的细胞负载量最大化,微球的细胞粘附性质和细胞负载条件被优化,导致细胞负载量增加约4.2倍。使用低MW PLGA设计的多孔微球有望作为角膜内皮细胞的输送系统,用于角膜内皮的再生。

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