A simple chemiluminescent method for the quantification of exosomes based on horseradish peroxidase adsorbed on two-dimensional nanomaterials

化学 化学发光 辣根过氧化物酶 纳米材料 脂质体 微泡 纳米复合材料 纳米颗粒 吸附 鲁米诺 纳米技术 色谱法 有机化学 生物化学 小RNA 材料科学 基因
作者
Meilin Li,Yifan Yu,Shanshan Li,Feiqian Wang,Sile Hong,Yinuo Sun,Aiping Fan
出处
期刊:Talanta [Elsevier BV]
卷期号:275: 126156-126156 被引量:7
标识
DOI:10.1016/j.talanta.2024.126156
摘要

The development of simple methods for the isolation and quantification of exosomes in biological samples is important. By using the typical two-dimensional (2D) nanomaterials, graphene oxide (GO), the present work first studied the interaction of liposomes with the nanocomposites formed by adsorbing HRP on the GO surface and found the presence of liposomes led to the release of HRP from the GO surface to the solution phase triggering the luminol-H2O2 chemiluminescence (CL) reaction to emit light. Benefiting from the similarity of exosomes to liposomes in both composition and morphology aspects, the GO-HRP nanocomposites with a mass ratio of 120:1 and 160:1 were employed for the quantitative detection of exosomes in 100-fold diluted serum samples. The whole detection process took about 15 min and as low as 3.2 × 102 particles μL-1 of exosomes could be sensitively detected. In addition to GO-HRP nanocomposites, the CL responses of other nanocomposites obtained from adsorbing HRP on other 2D nanomaterials such as layered MoS2 for exosomes were also tested. MoS2-HRP exhibited similar behavior and the LODs for the detection of exosomes were 5.8 × 102 particles μL-1. The proposed assays were a biomarker-independent quantitative method that achieved the quantification of exosomes in serum samples directly without an isolation process.
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