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Quantitative and simultaneous detection of two inflammation biomarkers via a fluorescent lateral flow immunoassay using dual-color SiO2@QD nanotags.
Yang, Xingsheng; Liu, Xiaoxian; Gu, Bing; Liu, Haifeng; Xiao, Rui; Wang, Chongwen; Wang, Shengqi.
Afiliação
  • Yang X; College of Life Sciences, Anhui Agricultural University, Hefei, 230036, People's Republic of China.
  • Liu X; Beijing Institute of Radiation Medicine, Beijing, 100850, People's Republic of China.
  • Gu B; College of Life Sciences, Anhui Agricultural University, Hefei, 230036, People's Republic of China.
  • Liu H; Beijing Institute of Radiation Medicine, Beijing, 100850, People's Republic of China.
  • Xiao R; Medical Technology Institute of Xuzhou Medical University, Xuzhou, 221004, People's Republic of China.
  • Wang C; Department of Laboratory Medicine, Affiliated Hospital of Xuzhou Medical University, Xuzhou, 221004, People's Republic of China.
  • Wang S; College of Life Sciences, Anhui Agricultural University, Hefei, 230036, People's Republic of China.
Mikrochim Acta ; 187(10): 570, 2020 09 17.
Article em En | MEDLINE | ID: mdl-32939582
ABSTRACT
An on-site detection strategy is reported based on dual-color SiO2@quantum dot (QD)-integrated lateral flow immunoassay (LFA) strip to realize the quantitative and simultaneous detection of C-reactive protein (CRP) and procalcitonin (PCT) in serum. The dual-color SiO2@QD nanotags with monodispersity and excellent luminescence were synthesized using polyethyleneimine-mediated electrostatic adsorption of dense red CdSe/ZnS-COOH (excitation/emission 365/625 nm) or green CdSe/ZnS-COOH (excitation/emission 365/525 nm) QDs on the surface of 180 nm SiO2 spheres and were conjugated with anti-PCT and anti-CRP monoclonal antibodies, as stable and fluorescent-enhanced QD nanotags in the LFA system. The use of SiO2@QDs with two different fluorescent signals caused the sensitivity and specificity of the multiplex LFA system. As a result, the proposed assay provided a wide logarithmic determination range with a CRP quantitative range of 0.5-103 ng/mL and PCT quantitative range of 0.05-103 ng/mL. The limits of detection (LODs) of CRP and PCT reached 0.5 and 0.05 ng/mL, respectively. The SiO2@QD-based LFA showed great potential as rapid detection tool for the simultaneous monitoring of CRP and PCT in serum sample.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína C-Reativa / Imunoensaio / Biomarcadores / Inflamação Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mikrochim Acta Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína C-Reativa / Imunoensaio / Biomarcadores / Inflamação Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mikrochim Acta Ano de publicação: 2020 Tipo de documento: Article