期刊
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 406, 期 22, 页码 5379-5387出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00216-014-7964-8
关键词
Lp(a); Screen-printed electrode; Integrated amperometric immunosensor; Human serum
资金
- Spanish Ministerio de Economia y Competitividad Research [CTQ2012-34238]
- AVANSENS Program, Comunidad de Madrid [S2009PPQ-1642]
- Spanish Ministerio de Ciencia e Innovacion
A novel strategy for the construction of a disposable integrated amperometric immunosensor for the sensitive and rapid determination of lipoprotein(a) (Lp(a)), an important predictor of cardiovascular disease risk, in human serum is reported. The approach uses a sandwich format involving the covalent immobilization of selective capture antibodies (antiLp(a)) on the surface of N-[N (alpha),N (alpha)-bis(carboxymethyl)-lysine]-12-mercaptododecanamide (HS-NTA)-modified screen-printed carbon electrodes (SPCEs). After a blocking step with skimmed milk, the modified antiLp(a)-SPCEs were incubated with a mixture solution containing the target analyte and a fixed concentration of a specific biotinylated antibody (biotin-antiLp(a)) and a streptavidin-horseradish peroxidase (HRP) (Strep-HRP) conjugate. The amperometric responses of the resulting immunosensor at -0.10 V (vs an Ag pseudo-reference electrode), upon addition of 3,3',5,5'-tetramethylbenzidine (TMB) as electron transfer mediator and H2O2 as the enzyme substrate, were used to monitor the extent of the immunoreactions. The developed methodology exhibited a wide range of linearity between 0.02 and 10 mu g mL(-1), a low detection limit (LOD) of 8 ng mL(-1), and a great selectivity against other serum components. The usefulness of the Lp(a) immunosensor was demonstrated by analyzing spiked serum samples as well as a reference serum containing a certified Lp(a) content.
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