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Encapsulation of BSA in polylactic acid–hyperbranched polyglycerol conjugate nanoparticles: preparation, characterization, and release kinetics

机译:BSA在聚乳酸-超支化聚甘油共轭纳米颗粒中的包封:制备,表征和释放动力学

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摘要

Nanoparticles based on an amphiphilic copolymer with polylactic acid (PLA) grafted onto hyperbranched polyglycerol (HPG) were prepared by the use of BSA as a model protein. The characteristics of the nanoparticles were evaluated using particle size analyzer, transmission electron microscopy, and X-ray photoelectron spectroscopy. The secondary structure of BSA released from nanoparticles were analysed by circular dichroism experiments. Cell viability of nanoparticles was also evaluated by using NIH 3T3 cells. The mechanism of BSA release was studied by fitting experimental data to three model equations. Results indicated that BSA diffusion and the polymeric relaxation jointly governed the overall release process. The detailed analysis of BSA release was performed using the first-order kinetic model equation, which gave a good fit to the experimental release data. The influence of different copolymer structures and BSA loading capacities on release profiles were also evaluated for the potential of using nanoparticles as controlled release protein delivery systems.
机译:通过使用BSA作为模型蛋白,制备了基于两亲共聚物的接枝到超支化聚甘油(HPG)上的聚乳酸(PLA)的纳米粒子。使用粒度分析仪,透射电子显微镜和X射线光电子能谱评估了纳米颗粒的特性。通过圆二色性实验分析了从纳米颗粒释放的BSA的二级结构。纳米颗粒的细胞生存力也通过使用NIH 3T3细胞进行了评估。通过将实验数据拟合到三个模型方程来研究BSA释放的机理。结果表明,BSA的扩散和聚合物的松弛共同控制着整个释放过程。使用一阶动力学模型方程对BSA释放进行了详细的分析,这与实验释放数据非常吻合。还评估了不同共聚物结构和BSA负载量对释放曲线的影响,以探讨使用纳米颗粒作为控释蛋白递送系统的潜力。

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