分散性
纳米颗粒
粒径
连接器
化学
色谱法
药物输送
纳米技术
体积热力学
牛血清白蛋白
材料科学
化学工程
有机化学
计算机科学
工程类
物理化学
物理
操作系统
量子力学
作者
Ali Jahanban‐Esfahlan,Siavoush Dastmalchi,Soodabeh Davaran
标识
DOI:10.1016/j.ijbiomac.2016.05.032
摘要
The current study tried to establish a simple and fast method for the preparation of BSA and HSA nanoparticles, based on an improved desolvation procedure under the aspect of a controllable particle size around 100nm for drug delivery applications. The Procedure used for the nanoparticles preparation was simplified by using a designed apparatus for controlling the addition of ethanol and it was used instead of conventional tubing pump which enabled the preparation of nanoparticles under defined conditions. By using EDC as cross-linker instead of glutharaldehyde, the time of nanoparticles preparation procedure was reduced to 3h. Several factors of the preparation process, such as the volume of the albumin solution, desolvating agent volume, the amount of cross-linker, the presence of salts and protein concentration were evaluated. Nanoparticles with smaller size were obtained under experimental conditions without the presence of salts or the use of buffers, 250mg of protein/4ml water, 5mg cross-linker, the addition of 4 and 8ml ethanol by using the designed apparatus to the HSA and BSA solution, respectively. By using this improved method, BSA and HSA nanoparticles of the size around 100nm and polydispersity below 0.2 were obtained.
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