Literature DB >> 752035

Some limitations of using equilibrium dialysis to study human serum albumin-testosterone interaction.

G W Moll, R L Rosenfield.   

Abstract

The apparent association constant of testosterone binding to pure human serum albumin was found to be significantly less at 5 g/dl (1.79 x 10(4) M-1) than at 1 g/dl (2.29 x 10(4) M-1). This demonstrates that the common assumption that binding site characteristics are constant with serum protein dilution is not strictly valid. Determination of the percent free testosterone at normal serum protein concentrations by equilibrium dialysis may also be in error by 20% or more due to fluid shifts within the test system.

Entities:  

Mesh:

Substances:

Year:  1978        PMID: 752035     DOI: 10.1210/jcem-46-3-501

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  2 in total

1.  Determination of protein binding by in vitro charcoal adsorption.

Authors:  J Yuan; D C Yang; J Birkmeier; J Stolzenbach
Journal:  J Pharmacokinet Biopharm       Date:  1995-02

Review 2.  A Reappraisal of Testosterone's Binding in Circulation: Physiological and Clinical Implications.

Authors:  Anna L Goldman; Shalender Bhasin; Frederick C W Wu; Meenakshi Krishna; Alvin M Matsumoto; Ravi Jasuja
Journal:  Endocr Rev       Date:  2017-08-01       Impact factor: 25.261

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.