2014
DOI: 10.1016/j.talanta.2013.11.063
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Surface plasmon resonance immunoassay for the detection of the TNFα biomarker in human serum

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Cited by 59 publications
(39 citation statements)
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References 31 publications
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“…By adding gold nanorods, detection limits for TNF-α were reduced by 40-fold in an SPR imaging study [229]. Using gold nanoparticles and an approach to reduce non-specific binding, TNF-α was detected down to 54.9 pg/mL in spiked human serum [230]. To determine the different TH1 responses from cells circulating in the blood, Rice and colleagues used SPR imaging [231].…”
Section: Optical Methodsmentioning
confidence: 99%
“…By adding gold nanorods, detection limits for TNF-α were reduced by 40-fold in an SPR imaging study [229]. Using gold nanoparticles and an approach to reduce non-specific binding, TNF-α was detected down to 54.9 pg/mL in spiked human serum [230]. To determine the different TH1 responses from cells circulating in the blood, Rice and colleagues used SPR imaging [231].…”
Section: Optical Methodsmentioning
confidence: 99%
“…Another study has demonstrated a further improvement in detection sensitivity by introducing a number of changes in the assays. While using the MUA coating for antibiofouling, the mass of the target analyte was increased using AuNPs as well as secondary antibodies, which achieved a DL of 54.9 pg/mL for TNF-α in spiked human urine [118]. Beyond these strategies such as novel antibiofouling coatings and the addition of tags for additional mass to improve sensitivity, novel scaffolds derived from albumin binding domains (ABD) of protein G were also engineered for the detection of IFN-γ as superior biorecognition elements relative to primary capture antibodies [119].…”
Section: Cytokine Sensors With Various Optical Modes Of Detectionmentioning
confidence: 99%
“…This assay allowed the researchers to spontaneously monitor IL-6 secretion by LPS stimulated human fibroblast MRC5-CVI cells. More recently, Martinez-Perdigueroa et al [75] introduced gold nanoparticles, instead of the secondary antibodies, for signal amplification. This method improved TNF-α detection sensitivity to 11.6 pg/mL (211fM) and 54.4 pg/mL (989 fM) in spiked buffer and human serum, respectively.…”
Section: Label-free Cytokine Biosensingmentioning
confidence: 99%