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Preparation and characterization of poly(DL-lactide-co-glycolide) microspheres for controlled release of human growth hormone

机译:聚(DL-丙交酯-共-乙交酯)微球的制备与表征

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摘要

The purpose of this research was to assess the physicochemical properties of a controlled release formulation of recombinant human growth hormone (rHGH) encapsulated in poly(D,L-lactide-co-glycolide) (PLGA) composite microspheres. rHGH was loaded in poly(acryloyl hydroxyethyl) starch (acHES) microparticles, and then the protein-containing microparticles were encapsulated in the PLGA matrix by a solvent extraction/evaporation method. rHGH-loaded PLGA microspheres were also prepared using mannitol without the starch hydrogel microparticle microspheres for comparison. The detection of secondary structure changes in protein was investigated by using a Fourier Transfer Infrared (FTIR) technique. The composite microspheres were spherical in shape (44.6±2.47 μm), and the PLGA-mannitol microspheres were 39.7±2.50 μm. Drug-loading efficiency varied from 93.2% to 104%. The composite microspheres showed higher overall drug release than the PLGA/mannitol microspheres. FTIR analyses indicated good stability and structural integrity of HGH localized in the microspheres. The PLGA-acHES composite microsphere system could be useful for the controlled delivery of protein drugs.
机译:这项研究的目的是评估封装在聚(D,L-丙交酯-乙交酯-乙交酯)(PLGA)复合微球中的重组人生长激素(rHGH)的控释制剂的理化性质。将rHGH加载到聚(丙烯酰基羟乙基)淀粉(acHES)微粒中,然后通过溶剂萃取/蒸发法将含蛋白质的微粒封装在PLGA基质中。还使用不含淀粉水凝胶微粒微球的甘露醇制备了载有rHGH的PLGA微球进行比较。通过使用傅立叶转移红外(FTIR)技术研究了蛋白质二级结构变化的检测。复合微球为球形(44.6±2.47μm),PLGA-甘露醇微球为39.7±2.50μm。载药效率在93.2%至104%之间。复合微球比PLGA /甘露醇微球显示出更高的总体药物释放。 FTIR分析表明,HGH位于微球中,具有良好的稳定性和结构完整性。 PLGA-acHES复合微球系统可用于控制蛋白质药物的递送。

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