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首页> 外文期刊>The Journal of Supercritical Fluids >Controllable preparation and formation mechanism of BSA microparticles using supercritical assisted atomization with an enhanced mixer
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Controllable preparation and formation mechanism of BSA microparticles using supercritical assisted atomization with an enhanced mixer

机译:利用增强混合器超临界辅助雾化可控地制备BSA微粒和形成机理

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摘要

Supercritical fluid assisted atomization introduced by a hydrodynamic cavitation mixer (SAA-HCM) was used to prepare bovine serum albumin (BSA) microparticles. Water was used as the sole solvent. A hydrodynamic cavitation mixer was applied to improve mass transfer and achieve a continuous near-thermodynamic-equilibrium solubilization of SC-CO2 in the liquid solution. Under the different conditions, the prepared BSA microparticles had various morphologies, such as corrugated particles, smooth hollow spherical particles and cup particles, with particle diameters ranging from 0.3 to 5 μm. The microparticle formation process was elucidated with the shell formation and central bubble mechanism. Compared to native BSA, BSA microparticles did not show significant change in primary structure, according to the results of sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The secondary structure of BSA was characterized by Fourier transform infrared spectroscopy (FT-IR). No new peaks were observed after SAA-HCM processing. In addition, the crystalline structure of the BSA microparticles was demonstrated to be amorphous because of the sudden supersaturation in the precipitation process. The SAA-HCM process is expected to be a promising technique for producing microparticles suitable for pulmonary delivery of therapeutic macromolecules.
机译:通过水力空化混合器(SAA-HCM)引入的超临界流体辅助雾化来制备牛血清白蛋白(BSA)微粒。水用作唯一的溶剂。使用液力空化混合器来改善传质并在液体溶液中实现SC-CO2的连续近乎热力学的平衡溶解。在不同的条件下,制备的BSA微粒具有多种形态,例如波纹状颗粒,光滑的空心球形颗粒和杯状颗粒,粒径范围为0.3至5μm。通过壳形成和中心气泡机理阐明了微粒形成过程。根据十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)的结果,与天然BSA相比,BSA微粒的一级结构没有显着变化。 BSA的二级结构通过傅立叶变换红外光谱(FT-IR)进行了表征。 SAA-HCM处理后未观察到新的峰。此外,由于沉淀过程中突然过饱和,证明了BSA微粒的晶体结构为非晶态。 SAA-HCM工艺有望成为生产适用于肺部输送治疗性大分子的微粒的有前途的技术。

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