2018
DOI: 10.1016/j.jpba.2017.11.064
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Immunofluorescence–based biosensor for the determination of dengue virus NS1 in clinical samples

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Cited by 35 publications
(23 citation statements)
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“…As shown in Fig C in S1 File, the limit of detection (LOD) was calculated by the following equation LOD = 3 (σ/ S ) [43], where, σ is the standard deviation and S is the sensitivity and LOD of our sensor system was found to be 1.49 μg/mL which is slightly lower or comparable to that of the previously reported biosensor [1, 44]. However, it is noteworthy that LOD value in our sensor is close to the level of NS1 in primary (0.04 to 2 μg/mL) and secondary DENV infection (0.01 to 2 μg/mL) in patients [8, 9] suggesting quite acceptable for clinical testing. Importantly, a strong linearity with good correlation (regression coefficient R 2 = 0.91) between Δ I % and NS1 concentration was seen in ranging from 0.003 to 1.25 μg/mL (inset in Fig 4C).…”
Section: Resultssupporting
confidence: 69%
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“…As shown in Fig C in S1 File, the limit of detection (LOD) was calculated by the following equation LOD = 3 (σ/ S ) [43], where, σ is the standard deviation and S is the sensitivity and LOD of our sensor system was found to be 1.49 μg/mL which is slightly lower or comparable to that of the previously reported biosensor [1, 44]. However, it is noteworthy that LOD value in our sensor is close to the level of NS1 in primary (0.04 to 2 μg/mL) and secondary DENV infection (0.01 to 2 μg/mL) in patients [8, 9] suggesting quite acceptable for clinical testing. Importantly, a strong linearity with good correlation (regression coefficient R 2 = 0.91) between Δ I % and NS1 concentration was seen in ranging from 0.003 to 1.25 μg/mL (inset in Fig 4C).…”
Section: Resultssupporting
confidence: 69%
“…Some reports suggest that the glycoprotein, nonstructural 1 (NS1), is a useful biomarker of infection because of its release and high level accumulation at concentrations up to 50 μg/mL in dengue patients [6, 7]. In the clinic, serum NS1 levels range from 0.04 to 2 μg/mL in patients with primary DENV infection and from 0.01 to 2 μg/mL in those with secondary infection [8, 9]. Therefore, a number of commercial rapid kits for DENV NS1 detection have been developed and characterized [3, 8, 1013].…”
Section: Introductionmentioning
confidence: 99%
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“…[ 31–33 ] Two key aspects that can be modified in ELISA‐IFA to further improve its performance and functionality are the proper immobilization of capture biomolecules and the use of optimal surface blocking agents to reduce the background noise often associated with fluorescence‐based assays. [ 45–47 ] For immobilization of biorecognition elements, contact printing and noncontact printing strategies have been widely used to generate microarrays of biorecognition elements (e.g., antibodies) using desired chemical linkers (e.g., amine or carboxyl groups). [ 48–50 ] The microarrays shape, diameter, thickness, homogeneity, and binding mechanism are important attributes to evaluate the efficacy of different microarray biosensing surface strategies.…”
Section: Introductionmentioning
confidence: 99%