Possibilities and limitations of current technologies for quantification of biological extracellular vesicles and synthetic mimics

Sybren L N Maas, Jeroen de Vrij, Els J van der Vlist, Biaina Geragousian, Louis van Bloois, Enrico Mastrobattista, Raymond M Schiffelers, Marca H M Wauben, Marike L D Broekman, Esther N M Nolte-'t Hoen*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

211 Citations (Scopus)
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Abstract

Nano-sized extracelullar vesicles (EVs) released by various cell types play important roles in a plethora of (patho)physiological processes and are increasingly recognized as biomarkers for disease. In addition, engineered EV and EV-inspired liposomes hold great potential as drug delivery systems. Major technologies developed for high-throughput analysis of individual EV include nanoparticle tracking analysis (NTA), tunable resistive pulse sensing (tRPS) and high-resolution flow cytometry (hFC). Currently, there is a need for comparative studies on the available technologies to improve standardization of vesicle analysis in diagnostic or therapeutic settings. We investigated the possibilities, limitations and comparability of NTA, tRPS and hFC for analysis of tumor cell-derived EVs and synthetic mimics (i.e. differently sized liposomes). NTA and tRPS instrument settings were identified that significantly affected the quantification of these particles. Furthermore, we detailed the differences in absolute quantification of EVs and liposomes using the three technologies. This study increases our understanding of possibilities and pitfalls of NTA, tRPS and hFC, which will benefit standardized and large-scale clinical application of (engineered) EVs and EV-mimics in the future.

Original languageEnglish
Pages (from-to)87-96
Number of pages10
JournalJournal of Controlled Release
Volume200
DOIs
Publication statusPublished - 28 Feb 2015
Externally publishedYes

Bibliographical note

Copyright © 2015. Published by Elsevier B.V.

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