| Literature DB >> 28374584 |
Chaoxiang Chen1, Shaobin Zhu1, Shuo Wang1, Wenqiang Zhang1, Yu Cheng1, Xiaomei Yan1.
Abstract
Drug-encapsulated liposomes have been considered the most clinically acceptable drug-delivery systems. However, current methods fall short in the quantitative characterization of individual nanoliposomes because of their small sizes and large heterogeneity. Here, we report a high-throughput method for the absolute quantification of particle size, drug content, fraction of drug encapsulation, and particle concentration of liposomal nanomedicines at the single-particle level. A laboratory-built high-sensitivity flow cytometer was used to simultaneously detect the side-scatter and fluorescence signals generated by individual nanomedicine particles at a speed up to 10 000 nanoparticles/min. To cope with the size dependence of the refractive index of liposomal nanomedicines, different sizes of doxorubicin-loaded liposomes were fabricated and characterized to serve as the calibration standards for the measurement of both particle size and drug content. This method provides a highly practical platform for the characterization of liposomal nanomedicines, and broad applications can be envisioned.Entities:
Keywords: doxorubicin-encapsulated liposomes; flow cytometry; nanomedicine; nanoparticle characterization; single-particle detection
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Year: 2017 PMID: 28374584 DOI: 10.1021/acsami.7b01867
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229