Literature DB >> 18387858

Simultaneous determination of prednisolone, prednisone, cortisol, and cortisone in plasma by GC-MS: estimating unbound prednisolone concentration in patients with nephrotic syndrome during oral prednisolone therapy.

Hiromi Shibasaki1, Hideaki Nakayama, Takashi Furuta, Yasuji Kasuya, Mari Tsuchiya, Akinori Soejima, Akira Yamada, Toshihiko Nagasawa.   

Abstract

Individual variability of the pharmacokinetics of prednisolone based on the unbound concentration in plasma is of significant clinical consideration. The unbound concentrations of prednisolone were measured in 10 patients with nephrotic syndrome, two patients with systemic lupus erythematosus, and one patient with dermatomyositis by examining protein bindings of prednisolone on one or more occasions during prednisolone treatment. In this study, plasma concentrations of prednisolone, prednisone, cortisol, and cortisone were simultaneously analyzed by GC-MS by using stable isotope-labeled internal standards. Equilibrium dialysis was employed to accurately estimate the unbound fractions of prednisolone in plasma. The unbound fraction of prednisolone changed depending on plasma total prednisolone concentration and plasma albumin concentration. The unbound fraction of prednisolone (Y) is calculated: Y=(-0.0101x' + 0.0736) x + 10.23, where x' is the plasma albumin concentration and x is the total prednisolone concentration. The estimated concentrations of unbound prednisolone by using the above equation were in good agreement with the measured concentrations of unbound prednisolone. Since the protein binding of prednisolone did not change in the presence of prednisone (114.0 ng/ml), it appeared that prednisone produced from the therapeutic dose of prednisolone did not affect the unbound fraction of prednisolone.

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Year:  2008        PMID: 18387858     DOI: 10.1016/j.jchromb.2008.03.003

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  6 in total

1.  Development and validation of a fast and sensitive bioanalytical method for the quantitative determination of glucocorticoids--quantitative measurement of dexamethasone in rabbit ocular matrices by liquid chromatography tandem mass spectrometry.

Authors:  Ravinder Earla; Sai H S Boddu; Kishore Cholkar; Sudharshan Hariharan; Jwala Jwala; Ashim K Mitra
Journal:  J Pharm Biomed Anal       Date:  2010-01-18       Impact factor: 3.935

2.  Tetra- and Penta-Cyclic Triterpenes Interaction with Lipid Bilayer Membrane: A Structural Comparative Study.

Authors:  Rola Abboud; Catherine Charcosset; Hélène Greige-Gerges
Journal:  J Membr Biol       Date:  2016-01-13       Impact factor: 1.843

3.  Toxicology study for magnetic injection of prednisolone into the rat cochlea.

Authors:  M Shimoji; B Ramaswamy; M I Shukoor; P Benhal; A Broda; S Kulkarni; P Malik; B McCaffrey; J-F Lafond; A Nacev; I N Weinberg; B Shapiro; D A Depireux
Journal:  Eur J Pharm Sci       Date:  2018-06-19       Impact factor: 4.384

4.  Outcome of participants with nephrotic syndrome in combined clinical trials of lupus nephritis.

Authors:  Liliana Michelle Gomez Mendez; Matthew D Cascino; Tamiko R Katsumoto; Paul Brakeman; Paul Brunetta; David Jayne; Maria Dall'Era; Brad Rovin; Jay Garg
Journal:  Lupus Sci Med       Date:  2019-02-04

5.  Plasma and ocular prednisolone disposition after oral treatment in cats.

Authors:  María J Del Sole; Paula Schaiquevich; Marcelo A Aba; Carlos E Lanusse; Laura Moreno
Journal:  Biomed Res Int       Date:  2013-08-29       Impact factor: 3.411

6.  A Metabolomic Approach for Predicting Diurnal Changes in Cortisol.

Authors:  Jarrett Eshima; Trenton J Davis; Heather D Bean; John Fricks; Barbara S Smith
Journal:  Metabolites       Date:  2020-05-13
  6 in total

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