2019
DOI: 10.1039/c9nr04050a
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An aptamer-based new method for competitive fluorescence detection of exosomes

Abstract: An aptamer-based low-cost sensitive competitive fluorescence detection method was developed to detect exosomes at concentrations as low as 1.0 × 105 particles per μL.

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Cited by 135 publications
(76 citation statements)
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“…[21][22][23][24][25] These advantages enable aptamers to be a promising receptor, with diverse applications for in vitro and in vivo diagnosis. [26][27][28][29][30][31][32][33][34][35][36][37][38][39] In addition to the choice of receptor, it is also important to develop amplication methods to detect COVID-19 with high sensitivity. Toward this goal, the proximity ligation immunoassay (PLA) has been recently developed as a unique signal amplication approach, 40 in which a protein target is detected by translating antibody-protein binding events into ampliable DNA sequences for subsequent real-time polymerase chain reaction quantication.…”
Section: Introductionmentioning
confidence: 99%
“…[21][22][23][24][25] These advantages enable aptamers to be a promising receptor, with diverse applications for in vitro and in vivo diagnosis. [26][27][28][29][30][31][32][33][34][35][36][37][38][39] In addition to the choice of receptor, it is also important to develop amplication methods to detect COVID-19 with high sensitivity. Toward this goal, the proximity ligation immunoassay (PLA) has been recently developed as a unique signal amplication approach, 40 in which a protein target is detected by translating antibody-protein binding events into ampliable DNA sequences for subsequent real-time polymerase chain reaction quantication.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, considering the importance of exosomes in the liquid biopsy of cancer, many studies have explored new detection techniques over the past few decades. 16 A series of novel technologies have been developed for the determination of exosomes, including uorescence detection, 17 electrochemical biosensors, 5,14,18,19 immunosensors, 13,20 surface plasmon resonance (SPR), [21][22][23] microuidic devices, 21 electrochemiluminescence, 24 aptasensors, 25 and spectroscopic analysis. 26 However, these established exosome assays usually involve labour-intensive steps and require extended quantitative protocols and expensive laboratory infrastructures.…”
Section: Introductionmentioning
confidence: 99%
“…The CDI was used to activate the silanol groups on the silica particle surface, promoting the conjugation process to the primary amine groups of streptavidin molecules. [ 47,48 ] The resultant particles were then modified with biotinylated CD63 aptamer, containing a sequence of 32 bases (CACCCCACCTCGCTCCCGTGACACTAATGCTA), [ 49 ] for specific recognition of exosomes. As such, if fluorescent‐labeled exosomes are present in a solution that is mixed with aptamer‐conjugated silica particles, they will be captured by the silica particles.…”
Section: Resultsmentioning
confidence: 99%