Literature DB >> 9925341

High-performance frontal analysis for drug-protein binding study.

A Shibukawa1, Y Kuroda, T Nakagawa.   

Abstract

High-performance frontal analysis (HPFA) is a novel analytical method which enables simultaneous determination of total and unbound drug concentrations under drug-plasma protein binding condition. HPFA can be achieved using separation systems such as HPLC and CE. This paper deals with the principle and feature of HPFA method and its application to the stereoselective protein binding study. HPFA allows a simple analysis following direct sample injection, and does not suffer from undesirable drug adsorption on membrane nor leakage of bound drug through the membrane which are often encountered in conventional ultrafiltration and dialysis methods. HPFA can be easily incorporated into on-line HPLC system. By coupling HPFA with a chiral HPLC column, the unbound concentration of a racemic drug can be determined enantioselectively. The detection limit can be improved by coupling of HPFA with a preconcentration column. High-performance capillary electrophoresis/frontal analysis (HPCE/FA) enables to determine unbound concentrations enantioselectively with ultramicro injection volume, and is hence useful especially for the binding study of proteins which are scarce and difficult to obtain.

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Year:  1999        PMID: 9925341     DOI: 10.1016/s0731-7085(98)00201-5

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  5 in total

1.  High-performance frontal analysis of the binding of thyroxine enantiomers to human serum albumin.

Authors:  Tomoko Kimura; Keiko Nakanishi; Terumichi Nakagawa; Akimasa Shibukawa; Katsumi Matsuzaki
Journal:  Pharm Res       Date:  2005-04-07       Impact factor: 4.200

2.  Irreversible binding of an anticancer compound (BI-94) to plasma proteins.

Authors:  Nagsen Gautam; Rhishikesh Thakare; Sandeep Rana; Amarnath Natarajan; Yazen Alnouti
Journal:  Xenobiotica       Date:  2015-04-14       Impact factor: 1.908

3.  Biantennary glycans as well as genetic variants of alpha1-acid glycoprotein control the enantioselectivity and binding affinity of oxybutynin.

Authors:  Tomoko Kimura; Akimasa Shibukawa; Katsumi Matsuzaki
Journal:  Pharm Res       Date:  2006-05-02       Impact factor: 4.200

4.  Quantitation of unbound sunitinib and its metabolite N-desethyl sunitinib (SU12662) in human plasma by equilibrium dialysis and liquid chromatography-tandem mass spectrometry: application to a pharmacokinetic study.

Authors:  Rana Rais; Ming Zhao; Ping He; Linping Xu; John F Deeken; Michelle A Rudek
Journal:  Biomed Chromatogr       Date:  2012-01-18       Impact factor: 1.902

5.  Modulation of nonspecific binding in ultrafiltration protein binding studies.

Authors:  Kyoung-Jin Lee; Rachel Mower; Tom Hollenbeck; Jesus Castelo; Nikole Johnson; Perry Gordon; Patrick J Sinko; Kevin Holme; Yong-Hee Lee
Journal:  Pharm Res       Date:  2003-07       Impact factor: 4.200

  5 in total

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