Literature DB >> 9725495

Distribution of fenofibric acid in lipoprotein fractions of patients.

M Nobilis1, J Kvetina, P Anzenbacher, T Vontor, D Svoboda, M Brátová, D Solichová, Z Zadák, V Bláha, J Vlcek.   

Abstract

The antidyslipidemic agent fenofibrate (procetofen) is hydrolysed in vivo to its main active metabolite--fenofibric (procetofenic) acid. This metabolite is usually determined in pharmacokinetic studies, because plasma concentrations of fenofibrate are practically undetectable. Presented study is focussed on the distribution of fenofibric acid into lipoprotein (VLDL, LDL, IDL and HDL) fractions of human and (for comparison) minipig blood plasma, which has not been studied yet. In order to obtain more accurate results, a new HPLC method based on the use of newly synthetized internal standards was developed. Four homologues of fenofibric acid prepared have identical chromophoric part of their molecules and hence the same UV spectra as fenofibric acid. From this point of view, these standards are more suitable for determination of fenofibric acid than the formerly used ones--naproxen or bezafibrate. Fenofibric acid levels in the high density lipoprotein fraction has been shown to be significantly higher (in both human and minipig plasma) than in the other lipoprotein fractions. This fact may be explained by higher affinity of the fenofibric acid to proteins constituting major part of the high density lipoprotein fraction.

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Year:  1998        PMID: 9725495     DOI: 10.1007/BF03189353

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  16 in total

1.  Identification of a major metabolite of the new hypolipidaemic agent, isopropyl 2-(4'(p-chlorobenzoyl) phenoxy)-2-methylpropionate (procetofene) in humans by gas chromatography-mass spectrometry.

Authors:  L F Elsom; D R Hawkins; L F Chasseaud
Journal:  J Chromatogr       Date:  1976-08-04

Review 2.  Fenofibrate. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in dyslipidaemia.

Authors:  J A Balfour; D McTavish; R C Heel
Journal:  Drugs       Date:  1990-08       Impact factor: 9.546

3.  Rapid determination of procetofenic acid in plasma by high-performance liquid chromatography.

Authors:  M C Caturla; J Albaigés
Journal:  J Chromatogr       Date:  1982-01-08

4.  Gas--liquid chromatographic determination of procetofenic acid in human plasma and urine.

Authors:  J P Desager
Journal:  J Chromatogr       Date:  1978-01-01

Review 5.  Pharmacology of fenofibrate.

Authors:  M J Chapman
Journal:  Am J Med       Date:  1987-11-27       Impact factor: 4.965

6.  A systematic antilipidemic structure-activity relationship study was carried out on a series of alcoyl- and benzoyl-phenoxy-carboxylic acids.

Authors:  R Sornay; J Gurrieri; C Tourne; F J Renson; B Majoie; E Wülfert
Journal:  Arzneimittelforschung       Date:  1976

7.  Antilipidemic drugs. Part 4: The metabolic fate of the hypolipidemic agent isopropyl-[4'-(p-chlorobenzoyl)-2-phenoxy-2-methyl]-protionate (LF 178) in rats, dog and man.

Authors:  R R Brodie; L F Chasseaud; F F Elson; E R Franklin; T Taylor
Journal:  Arzneimittelforschung       Date:  1976

8.  Antilipidemic drugs. Part 6: LF 178 in man. A preliminary note on a multicenter investigation bearing on 393 subjects with pure or mixed forms of hyperlipidemia.

Authors:  B Wülfert; B Majoie; A de Ceaurriz
Journal:  Arzneimittelforschung       Date:  1976

9.  Atilipidemic drugs. Part 5: Evaluation of the hypolipidemic effect of LF 178 in 191 patients affected by the atherogenic form of endogenous hyperlipoproteinemia (types IIa, IIb and IV).

Authors:  J Rouffy; C Dreux; Y Goussault; R Dakkak; F J Renson
Journal:  Arzneimittelforschung       Date:  1976

10.  The metabolism and disposition of 14C-fenofibrate in human volunteers.

Authors:  A Weil; J Caldwell; M Strolin-Benedetti
Journal:  Drug Metab Dispos       Date:  1990 Jan-Feb       Impact factor: 3.922

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  1 in total

Review 1.  High-performance liquid chromatography-tandem mass spectrometry in the identification and determination of phase I and phase II drug metabolites.

Authors:  M Holcapek; L Kolárová; M Nobilis
Journal:  Anal Bioanal Chem       Date:  2008-03-15       Impact factor: 4.142

  1 in total

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