2015
DOI: 10.1016/j.bios.2015.04.040
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Target catalyzed hairpin assembly for constructing a ratiometric electrochemical aptasensor

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Cited by 53 publications
(11 citation statements)
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“…Ratiometric strategy eliminates false positive results brought by external factors in traditional detection strategies where analytes are embodied by a single signal, thus is more reliable and stable with good sensitivity and broad detection range. As a new hotspot in recent research of novel sensors, ratiometric strategy is promising to constitute a series of electrochemical DNA sensors or aptasensors. As one typical example, dual-signaling electrochemical aptasensor based on sandwich structure was reported . The developed ratiometric aptasensor showed good response toward thrombin with a LOD of 170 pM.…”
Section: Methods and Improvementsmentioning
confidence: 99%
“…Ratiometric strategy eliminates false positive results brought by external factors in traditional detection strategies where analytes are embodied by a single signal, thus is more reliable and stable with good sensitivity and broad detection range. As a new hotspot in recent research of novel sensors, ratiometric strategy is promising to constitute a series of electrochemical DNA sensors or aptasensors. As one typical example, dual-signaling electrochemical aptasensor based on sandwich structure was reported . The developed ratiometric aptasensor showed good response toward thrombin with a LOD of 170 pM.…”
Section: Methods and Improvementsmentioning
confidence: 99%
“…Gao et al have also demonstrated an amplified ratiometric electrochemical method for thrombin detection, but instead utilising target recycling to provide amplification (Figure 14c) [54]. In this instance, two hairpin DNA probes are employed: one as a target capture probe containing a thrombin-specific aptamer sequence and labelled with Fc, and the other as a support probe which is solid supported onto a AuE.…”
Section: Amplification Strategiesmentioning
confidence: 99%
“…Ratiometric electrochemical sensing can be achieved through either tagging both termini of nucleic acid capture probes bound to electrode surfaces with redox labels that have different oxidation potentials (29)(30)(31)(32)(33)(34)(35)(36)(37)(38)(39)(40)(41), manipulating host-guest or metal binding interactions on electrode surfaces with electrochemically distinguishable redox probes (42)(43)(44), or the use of redox-active probes which demonstrate a unique shift in oxidation potential selectively in the presence of the analyte (45)(46). For analytes that display target catalysis as a means of amplification within diagnostic assays, we have found the latter offers a number of benefits, such as improved reaction kinetics, since probes are not surface bound, and ease of analysis, as electrodes do not require modification prior to detection (47)(48).…”
Section: Ratiometric Electrochemical Detection Of Palladiummentioning
confidence: 99%