纳米粒子跟踪分析
外体
大小排阻色谱法
化学
动态光散射
粒径
纳米颗粒
杂质
色谱法
光散射
粒子(生态学)
微泡
分析化学(期刊)
材料科学
散射
纳米技术
生物化学
酶
光学
物理
有机化学
小RNA
物理化学
基因
海洋学
地质学
作者
Hirotaka Nishimura,Noritaka Hashii,Tomofumi Yamamoto,Yuchen Sun,Takumi Miura,Yoji Sato,Akiko Ishii‐Watabe
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2024-11-27
卷期号:16 (12): 1526-1526
被引量:1
标识
DOI:10.3390/pharmaceutics16121526
摘要
Background: Extracellular vesicles (EVs), including exosomes, are promising pharmaceutical modalities. They are purified from cell culture supernatant; however, the preparation may contain EVs with the desired therapeutic effects and different types of EVs, lipoproteins, and soluble proteins. Evaluating the composition of particulate impurities and the levels of protein impurities in final preparations is critical for quality control. However, few analytical methods can detect these impurities. Methods: We established and evaluated an analytical method using size-exclusion chromatography–multi-angle light scattering (SEC-MALS) for particle and protein impurity analyses of EV samples. Results: In the particle size distribution analysis of EV samples, SEC-MALS showed higher resolution compared with nanoparticle tracking analysis (NTA) and dynamic light scattering (DLS). MALS showed comparable accuracy and precision to that of other methods for particle size evaluation using polystyrene standard beads with 60, 100, or 200 nm diameter. Coupling SEC-MALS with UV detection quantitatively evaluated soluble protein impurities. Proteomic analysis on the SEC-MALS-fractionated samples identified different EV and lipoprotein marker proteins in different fractions. Conclusions: SEC-MALS can characterize EV preparations obtained from human adipose-derived mesenchymal stem cells, suggesting that it can evaluate the particle component composition in various EV samples and therapeutic exosome preparations.
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