2022
DOI: 10.1016/j.talanta.2021.123032
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A label-free colorimetric aptasensor based on split aptamers-chitosan oligosaccharide-AuNPs nanocomposites for sensitive and selective detection of kanamycin

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Cited by 32 publications
(11 citation statements)
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“…AuNPs-based aptasensors have been widely applied in the detection of various targets including chemical compounds, proteins, pesticides, toxins, and viruses [ 36 , 38 , 39 , 40 , 48 , 49 , 50 ]. Their simple preparation, rapid detection, and the fact that they do not require special instrumentation have made them the preferred choice for PoCT [ 51 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…AuNPs-based aptasensors have been widely applied in the detection of various targets including chemical compounds, proteins, pesticides, toxins, and viruses [ 36 , 38 , 39 , 40 , 48 , 49 , 50 ]. Their simple preparation, rapid detection, and the fact that they do not require special instrumentation have made them the preferred choice for PoCT [ 51 ].…”
Section: Resultsmentioning
confidence: 99%
“…If the analyte for the specific MRE is present, the MRE binds to the analyte instead of the AuNPs and the colour of the AuNPs will change from ruby red to purple/blue. Based on this principle, several AuNP-based optical aptasensors have been developed [ 36 , 37 , 38 , 39 , 40 ]. In this study, using this principle, a simple yet effective, specific, and rapid RBP-A-aptasensor for the detection of RBP4 was developed.…”
Section: Introductionmentioning
confidence: 99%
“…These are capable of binding specific targets with high affinity, specificity, and sensitivity [ 26 , 27 ]. The target molecule can be as simple as a metal ion, and can be as complex as large protein molecules such as cardiac troponin, or even cells [ 28 , 29 , 30 , 31 , 32 ]. Aptamers are designed by an easier, cheaper in vitro method called SELEX (systematic evolution of ligands by exponential enrichment) [ 33 , 34 ].…”
Section: Label and Label-free Aptasensorsmentioning
confidence: 99%
“…Molecular docking could simulate aptamer–ligand interactions and completely characterize complexes, 23 allowing for generating accurate three-dimensional (3D) models and the elucidation of detailed binding sites. 24 Ma et al 25 used molecular docking to predict the critical bases of aptamer binding to chloramphenicol, and then trimmed the 80-base aptamer to 30 bases for designing the biosensor. Through molecular docking, the recognition mechanism between the aptamer and target can be analyzed and quantified in detail to construct a highly sensitive and reliable apasensor, which involved a complementary sequence and competitive strategy.…”
Section: Introductionmentioning
confidence: 99%