Clinical Chemistry
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Clinical Chemistry 47: 1269-1278, 2001;
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(Clinical Chemistry. 2001;47:1269-1278.)
© 2001 American Association for Clinical Chemistry, Inc.

Articles

Supersensitive Time-resolved Immunofluorometric Assay of Free Prostate-specific Antigen with Nanoparticle Label Technology

Tero Soukka1a, Janika Paukkunen1, Harri Härmä1, Stefan Lönnberg1, Hanne Lindroos1 and Timo Lövgren1

1 Department of Biotechnology, University of Turku, Tykistökatu 6, FIN-20520 Turku, Finland.


aAuthor for correspondence. Fax 358-2-333-8050; e-mail tero.soukka{at}utu.fi.

Background: The extreme specific activity of the long-lifetime fluorescent europium(III) chelate nanoparticles and the enhanced monovalent binding affinity of multivalent nanoparticle-antibody bioconjugates are attractive for noncompetitive immunoassay.

Methods: We used a noncompetitive, two-step immunoassay design to measure free prostate-specific antigen (PSA). Europium(III) chelate nanoparticles (107 nm in diameter) were coated with a monoclonal anti-PSA antibody (intrinsic affinity, 6 x 109 L/mol). The nanoparticle-antibody bioconjugates had an average of 214 active binding sites per particle and a monovalent binding affinity of 7 x 1010 L/mol. The assay was performed in a low-fluorescence microtitration well passively coated with an another monoclonal anti-PSA antibody (affinity, 2 x 1010 L/mol), and the europium(III) fluorescence was measured directly from the bottom of the well by a standard time-resolved microtitration plate fluorometer.

Results: The detection limit (mean + 2 SD) was 0.040 ng/L (7.3 x 105 molecules/mL), and the dynamic detection range covered four orders of magnitude in a 3-h total assay time. The imprecision (CV) over the whole assay range was 2–10%. The detection limit of the assay was limited by the fractional nonspecific binding of the bioconjugate to the solid phase (0.05%), which was higher than the nonspecific binding of the original antibody (<0.01%).

Conclusions: The sensitivity of the new assay is equal to that of the ambient-analyte, microspot immunoassay and will be improved by use of optimized, high binding-site density nanoparticle-antibody bioconjugates with reduced nonspecific binding and improved monovalent binding affinity.




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