2016
DOI: 10.1016/j.aca.2016.02.024
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Multiplex electrochemiluminescence DNA sensor for determination of hepatitis B virus and hepatitis C virus based on multicolor quantum dots and Au nanoparticles

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Cited by 65 publications
(21 citation statements)
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“… Detection Methods Detection Target Linear Range Detection Limit Ref. ECA HBV DNA 0.4–10 nM 0.01 nM 41 ECA HBsAg 1 ng –10 µg mL −1 0.14 ng mL −1 42 ECA HBsAg 0.05–15 ng mL −1 20 pg mL −1 22 ECA anti-HBc 1–6 ng mL −1 0.03 ng mL −1 21 ECLA HBV DNA 0.5 pM–0.5 nM 0.082 pM 43 ECA HBV preS1 1 pM–50 pM 0.1 pM This study Abbreviations: ECA, electrochemical assay; ECLA, electrochemiluminescence assay; HBsAg, hepatitis B surface antigen; anti-HBc, antibodies to hepatitis B core protein. …”
Section: Resultsmentioning
confidence: 99%
“… Detection Methods Detection Target Linear Range Detection Limit Ref. ECA HBV DNA 0.4–10 nM 0.01 nM 41 ECA HBsAg 1 ng –10 µg mL −1 0.14 ng mL −1 42 ECA HBsAg 0.05–15 ng mL −1 20 pg mL −1 22 ECA anti-HBc 1–6 ng mL −1 0.03 ng mL −1 21 ECLA HBV DNA 0.5 pM–0.5 nM 0.082 pM 43 ECA HBV preS1 1 pM–50 pM 0.1 pM This study Abbreviations: ECA, electrochemical assay; ECLA, electrochemiluminescence assay; HBsAg, hepatitis B surface antigen; anti-HBc, antibodies to hepatitis B core protein. …”
Section: Resultsmentioning
confidence: 99%
“…Within the past five years, researchers have developed new B-CRSAs that take advantage of current technological advances, including functionalized carbon nanotube field effect transistor (FET) sensors, and metal oxide semiconductor (MOS) sensors, proposing devices with improved sensitivity, selectivity, and stability. With the development of more extensive and selective sensing mechanisms alongside advances in electronics and signal processing, B-CRSA devices have become smaller, more selective, and more sensitive, with fast data processing time and facile readout of vapor analysis [ 54 , 66 , 131 , 132 , 133 , 134 ].…”
Section: Future Directions and Remaining Challenges For B-crsa Diamentioning
confidence: 99%
“…These were incubated with target DNA, which prevented the binding of target DNA coated AuNPs in a dose-dependent manner. Subsequently, target DNA concentrations were determined by the quenching of QD electrochemoluminescence by AuNPs [ 76 ]. By employing these methods, the authors could detect HBV DNA with concentrations as low as 8.2 × 10 −14 M in human serum without PCR amplification.…”
Section: Combinations Of Different Nanoparticlesmentioning
confidence: 99%