微泡
外体
纳米医学
内吞循环
纳米技术
计算生物学
计算机科学
生物
材料科学
小RNA
细胞
内吞作用
纳米颗粒
遗传学
生物化学
基因
作者
Arnau Pallarès-Rusiñol,Mireia Bernuz,Silio Lima Moura,Carolina Fernández-Senac,Rosanna Rossi,Mercè Martı́,María Isabel Pividori
出处
期刊:Advances in Clinical Chemistry
日期:2022-12-20
卷期号:: 69-117
被引量:16
标识
DOI:10.1016/bs.acc.2022.09.002
摘要
There is growing demand for novel biomarkers that detect early stage disease as well as monitor clinical management and therapeutic strategies. Exosome analysis could provide the next advance in attaining that goal. Exosomes are membrane encapsulated biologic nanometric-sized particles of endocytic origin which are released by all cell types. Unfortunately, exosomes are exceptionally challenging to characterize with current technologies. Exosomes are between 30 and 200nm in diameter, a size that makes them out of the sensitivity range to most cell-oriented sorting or analysis platforms, i.e., traditional flow cytometers. The most common methods for targeting exosomes to date typically involve purification followed by the characterization and the specific determination of their cargo. The whole procedure is time consuming, requiring thus skilled personnel as well as laboratory facilities and benchtop instrumentation. The most relevant methodology for exosome isolation, characterization and quantification is addressed in this chapter, including the most up-to-date approaches to explore the potential usefulness of exosomes as biomarkers in liquid biopsies and in advanced nanomedicine.
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