2009
DOI: 10.1016/j.cca.2009.01.015
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Surface plasmon resonance immunoassay analysis of pituitary hormones in urine and serum samples

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Cited by 60 publications
(34 citation statements)
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“…The limit of detection, 0.005 ng/mL, was calculated as three times the standard deviation of the signals provided (n010) by using 0.1 ng/mL hGH as the noise estimate. This detection limit is much lower than that reported using the SPRbased methodology, 4 ng/mL [8,9]. Moreover, a limit of quantification of 0.017 ng/mL was calculated as ten times the standard deviation (n010) of the estimate .This good analytical performance can be attributed to the combination of two important practical advantages: the immunoconjugate preconcentration provided by functionalized MBs and the high sensitivity inherent to the voltammetric transduction used.…”
Section: Resultsmentioning
confidence: 91%
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“…The limit of detection, 0.005 ng/mL, was calculated as three times the standard deviation of the signals provided (n010) by using 0.1 ng/mL hGH as the noise estimate. This detection limit is much lower than that reported using the SPRbased methodology, 4 ng/mL [8,9]. Moreover, a limit of quantification of 0.017 ng/mL was calculated as ten times the standard deviation (n010) of the estimate .This good analytical performance can be attributed to the combination of two important practical advantages: the immunoconjugate preconcentration provided by functionalized MBs and the high sensitivity inherent to the voltammetric transduction used.…”
Section: Resultsmentioning
confidence: 91%
“…The dynamic range of linearity comprised between 0.01 and 100 ng/mL (r 00.998) covering four orders of magnitude in hGH concentration, with the equation i(μA)05.7 logC +11.6 (r00.992, n08). The lower part of this linearity range involves much lower concentrations than those achieved with a SPR immunosensor, 18-542 ng/mL [9]. The limit of detection, 0.005 ng/mL, was calculated as three times the standard deviation of the signals provided (n010) by using 0.1 ng/mL hGH as the noise estimate.…”
Section: Resultsmentioning
confidence: 99%
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“…The binding of the analyte causes a change in the refractive index, which can be detected without any signal amplification [62]. Matrix interferences are known to limit the suitability of SPR technology to analysis of clinical samples [63,64]. Nevertheless, SPR technology has been used for detecting analytes from saliva [63,65,66], urine, and serum [64], and it can be used in multianalyte assays [67,68].…”
Section: Label-free Methodsmentioning
confidence: 98%
“…13,14 This is particularly important for optical sensors, since the presence of blood cells in the sample can negatively affect the optical detection path and compromise accuracy. Detection technologies such as whispering gallerymode devices, 15 plasmon resonance devices, 16 and photonic crystals, 17 can benefit from the preremoval of nontargeted cells from whole blood to enhance the capture efficiency of targeted pathogens and proteins. In a clinical laboratory setting, plasma separation can simply be performed by centrifugation, whereas it remains a challenge at the POC, especially in resource-constrained settings due to lack of laboratory infrastructure.…”
Section: Introductionmentioning
confidence: 99%