32
Views
1
CrossRef citations to date
0
Altmetric
Original Articles

FREE THYROXINE SOLID-ANALOG IMMUNOASSAYS. INVESTIGATION OF THE ALBUMIN EFFECT ON THE ANTIBODY BINDING TO IMMOBILIZED THYROXINE-PROTEIN CONJUGATES

, , &
Pages 95-105 | Received 17 May 2001, Accepted 24 Jun 2001, Published online: 06 Feb 2007
 

ABSTRACT

A reliable one-step, analog-based FT4 immunoassay should be characterized by minimal binding of the serum thyroxine-binding proteins to thyroxine-analogs, used either as liquid-phase tracers or as solid-phase reagents. In this work, we investigated the effect of serum albumin concentration on the anti-T4 antibody binding to immobilized T4-protein conjugates with respect to the molecular weight (MW) and the T4-to-protein molar ratio of the conjugates. It was found that the presence of albumin in the serum sample, at concentrations up to 120 g/L, slightly decreased the antibody binding to the immobilized conjugates (less than 10%). In addition, this decrease was independent of both the MW and the T4-to-protein molar ratio of the conjugates. On the other hand, using the same conjugates as liquid-phase labeled analogs, the observed decrease ranged between 2 and 33%, depending on the MW of the conjugate. These findings indicate that the use of immobilized T4-protein conjugates may improve FT4 immunoassay reliability, concerning, especially, the issues of serum albumin concentration and/or affinity alterations.

Acknowledgments

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 757.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.