|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|866158||1470944||2017||8 صفحه PDF||سفارش دهید||دانلود رایگان|
• A multiplex lateral flow immunoassay for Extracellular vesicles detection has been developed.
• Colloidal gold and additional capture lines provided the best sensitivity.
• The limit of detection was of 3.4×06 EVs/µL with anti-CD81 and anti-CD9 as capture antibodies.
• This platform allows Point-of-care measurements based on biological vesicles determination.
Extracellular vesicles (EVs) are membrane-bound nanovesicles delivered by different cellular lineages under physiological and pathological conditions. Although these vesicles have shown relevance as biomarkers for a number of diseases, their isolation and detection still has several technical drawbacks, mainly related with problems of sensitivity and time-consumed. Here, we reported a rapid and multiple-targeted lateral flow immunoassay (LFIA) system for the detection of EVs isolated from human plasma. A range of different labels (colloidal gold, carbon black and magnetic nanoparticles) was compared as detection probe in LFIA, being gold nanoparticles that showed better results. Using this platform, we demonstrated that improvements may be carried out by incorporating additional capture lines with different antibodies. The device exhibited a limit of detection (LOD) of 3.4×106 EVs/µL when anti-CD81 and anti-CD9 were selected as capture antibodies in a multiple-targeted format, and anti-CD63 labeled with gold nanoparticles was used as detection probe. This LFIA, coupled to EVs isolation kits, could become a rapid and useful tool for the point-of-care detection of EVs, with a total analysis time of two hours.
Journal: Biosensors and Bioelectronics - Volume 87, 15 January 2017, Pages 38–45