Literature DB >> 6146673

Liquid chromatographic retention of beta-adrenoceptor antagonists: an index of lipid solubility.

R M Arendt, D J Greenblatt.   

Abstract

The in-vitro lipophilicity of nine beta-adrenoceptor antagonists was evaluated based on retention on a reverse-phase C-18 high-pressure liquid chromatographic (hplc) system at physiologic pH. Propranolol was by far the most lipophilic drug, while atenolol and sotolol were the least. Hplc retention was highly correlated (r = 0.92) with octanol: buffer partition coefficient. Thus hplc retention is a rapid and replicable approach to the determination of in-vitro lipophilicity that does not require radioactive drug.

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Year:  1984        PMID: 6146673     DOI: 10.1111/j.2042-7158.1984.tb04407.x

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  2 in total

Review 1.  Factors influencing drug protein binding in patients with end stage renal failure.

Authors:  R Vanholder; R De Smet; S Ringoir
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

2.  Kinetics, brain uptake, and receptor binding characteristics of flurazepam and its metabolites.

Authors:  L G Miller; D J Greenblatt; D R Abernethy; H Friedman; M D Luu; S M Paul; R I Shader
Journal:  Psychopharmacology (Berl)       Date:  1988       Impact factor: 4.530

  2 in total

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