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The role of surface charge in the desolvation process of gelatin: implications in nanoparticle synthesis and modulation of drug release

机译:表面电荷在明胶的去溶剂化过程中的作用:对纳米粒子合成和药物释放调节的影响

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摘要

The process of moving hydrophobic amino acids into the core of a protein by desolvation is important in protein folding. However, a rapid and forced desolvation can lead to precipitation of proteins. Desolvation of proteins under controlled conditions generates nanoparticles – homogeneous aggregates with a narrow size distribution. The protein nanoparticles, under physiological conditions, undergo surface erosion due to the action of proteases, releasing the entrapped drug/gene. The packing density of protein nanoparticles significantly influences the release kinetics. We have investigated the desolvation process of gelatin, exploring the role of pH and desolvating agent in nanoparticle synthesis. Our results show that the desolvation process, initiated by the addition of acetone, follows distinct pathways for gelatin incubated at different pH values and results in the generation of nanoparticles with varying matrix densities. The nanoparticles synthesized with varying matrix densities show variations in drug loading and protease-dependent extra- and intracellular drug release. These results will be useful in fine-tuning the synthesis of nanoparticles with desirable drug release profiles.
机译:通过去溶剂化将疏水性氨基酸移动到蛋白质核心的过程在蛋白质折叠中很重要。但是,快速而强制的去溶剂化作用可能导致蛋白质沉淀。在受控条件下对蛋白质进行去溶剂化处理可生成纳米颗粒,即均匀的聚集体,粒径分布狭窄。蛋白质纳米颗粒在生理条件下由于蛋白酶的作用而受到表面侵蚀,从而释放出被包裹的药物/基因。蛋白质纳米颗粒的堆积密度显着影响释放动力学。我们已经研究了明胶的去溶剂化过程,探索了pH和去溶剂剂在纳米颗粒合成中的作用。我们的结果表明,由添加丙酮引发的去溶剂化过程遵循明胶在不同pH值下孵育的独特途径,并导致生成具有不同基质密度的纳米颗粒。合成的具有不同基质密度的纳米颗粒显示出药物载量和蛋白酶依赖性细胞外和细胞内药物释放的变化。这些结果将有助于微调具有所需药物释放曲线的纳米颗粒的合成。

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