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首页> 外文期刊>European journal of pharmaceutical sciences >A facile approach for crosslinker free nano self assembly of protein for anti-tumor drug delivery: Factors' optimization, characterization and in vitro evaluation
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A facile approach for crosslinker free nano self assembly of protein for anti-tumor drug delivery: Factors' optimization, characterization and in vitro evaluation

机译:一种用于蛋白质的无交联剂纳米自组装抗肿瘤药物的简便方法:因子的优化,表征和体外评估

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摘要

We report crosslinker free self assembly of bovine serum albumin (BSA) and a hydrophobic payload pac-litaxel (PTX), into nanoparticles by harnessing the temperature driven unfolding of protein. To systematically study the effects of various factors responsible for the key attributes of the nanoparticles, a Resolution IV design was used. 20 formulations were made with pH, temperature, time of heating before and after addition of drug, stirring rate, protein concentration, and protein to drug ratio selected as independent variables. Particle size, encapsulation efficiency, yield and zeta potential were the response variables. Perturbation and Pareto charts were used to single out the important factors, while, mathematical equations and 3D surface charts have been used to describe the relationship between dependent and independent variables. Nanoparticles with size of 188-482 nm were observed with a highly negative zeta potential of -39.5 to -21.9.
机译:我们报告利用温度驱动的蛋白质解折叠,将牛血清白蛋白(BSA)和疏水性有效载荷pac-紫杉醇(PTX)交联剂自由自组装成纳米颗粒。为了系统地研究负责纳米颗粒关键属性的各种因素的影响,使用了决议IV设计。选择pH,温度,添加药物前后的加热时间,搅拌速率,蛋白质浓度和蛋白质与药物的比例作为独立变量,制成20种配方。粒度,包封效率,产率和ζ电势是响应变量。使用扰动图和帕累托图来选出重要因素,而使用数学方程式和3D表面图来描述因变量和自变量之间的关系。观察到大小为188-482 nm的纳米粒子,其zeta负电势极高,为-39.5至-21.9。

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