2016
DOI: 10.1016/j.ab.2016.01.011
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Colorimetric detection of bisphenol A based on unmodified aptamer and cationic polymer aggregated gold nanoparticles

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Cited by 66 publications
(19 citation statements)
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“…As shown in Fig. 2, P4 aptamer, as a singlestranded DNA, has a negative peak at 240-260 nm and a positive peak at 270-290 nm, which is in accordance with the previous record [20,31]. After adding P4, the value of the negative and positive peaks changed, but the location of the peaks did not shift.…”
Section: Characterization Of the Interaction Between P4 Aptamer And Asupporting
confidence: 87%
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“…As shown in Fig. 2, P4 aptamer, as a singlestranded DNA, has a negative peak at 240-260 nm and a positive peak at 270-290 nm, which is in accordance with the previous record [20,31]. After adding P4, the value of the negative and positive peaks changed, but the location of the peaks did not shift.…”
Section: Characterization Of the Interaction Between P4 Aptamer And Asupporting
confidence: 87%
“…In order to optimize the NaCl concentration, AuNPs were treated with different volumes of 2 M NaCl solution (0, 10,15,20,25,30,35, and 40 μL) and MOPS buffer were added to attain a total volume of 500 μL. After incubating for 5 min, A520 and A650 were recorded, and the minimum NaCl concentration that can fully induce aggregation of AuNPs was chosen.…”
Section: Optimization Of Detection Conditionsmentioning
confidence: 99%
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“…These disadvantages have prevented them from becoming widespread, making the capacity for on‐site detection rare. To facilitate the on‐site detection of BPA, aptamer‐based methods and enzyme‐linked immunosorbent assays (ELISAs) have been broadly investigated and developed . The use of aptamers and ELISA has allowed researchers to avoid the expense of purchasing high‐cost devices, making tremendous progress on the path toward on‐site detection.…”
Section: Introductionmentioning
confidence: 99%