聚合物
PLGA公司
纳米颗粒
聚合物降解
动力学
材料科学
化学工程
降级(电信)
分子质量
单体
粘度
摩尔质量分布
阿霉素
色谱法
化学
纳米技术
有机化学
复合材料
医学
外科
计算机科学
工程类
酶
物理
电信
化疗
量子力学
作者
Natalya Kumskova,Yu. V. Ermolenko,Nadezhda Osipova,Aleksey Semyonkin,Н. Р. Кильдеева,M. Yu. Gorshkova,Andrey M. Kovalskii,Tatyana Kovshova,Vadim V. Tarasov,J. Kreuter,Olga Maksimenko,Svetlana Gelperina
标识
DOI:10.1080/02652048.2020.1729885
摘要
Aims: To evaluate the influence of minor differences in molecular weights of commercially available low molecular weight PLGA grades on the kinetics of doxorubicin release from the nanoparticles.Methods: Three low-molecular weight 50/50 PLGA polymers were thoroughly characterised concerning intrinsic viscosity, molecular weight (Mw), acid value, and residual monomer content. The doxorubicin-loaded nanoparticles prepared using these polymers were evaluated concerning the kinetics of drug release and hydrolytic degradation.Results: The Mw of the polymers were slightly different: 10.2, 10.3, and 4.7 kDa. The nanoparticles obtained from the polymer with Mw of 4.7 kDa exhibited considerably higher rates of drug release and polymer degradation.Conclusion: In the case of low molecular weight PLGA grades even a few kilodaltons could be important for the batch-to-batch reproducibility of the nanoformulation parameters. These results bring forward the importance of in-house characterisation of the polymers to be used for the nanoparticle preparation.
科研通智能强力驱动
Strongly Powered by AbleSci AI