TLC determination of hydrophilicity parameter of some pyridinium aldoximes

Rudolf Laufer, Mária Báthori, Tamás Csermely, Georg Petroianu, Kamil Kuca, Noémi Tóth, Huba Kalász

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The chemical structures of certain drug candidates give only a minimum of lipophilicity. Investigation of their elution on reversed-phase materials was difficult, even when the water content of the mobile phase was changed. The dominative role of lipophilicity, either in the drugs' penetration or in the receptorial drug binding, is considered to be valid solely in the same chemical group of the various drugs. In the cases of extremely lipophobic (i.e., hydrophilic) compounds, both the determination or calculation of lipophilicity was difficult or impossible. This is the reason that a novel index, the TLC hydrophilicity parameter, should be introduced as a substitute for lipophilicity. Hydrophilicity can be preferrably determined using a planar stationary phase and an aqueous-organic mobile phase. Numerical data of hydrophilicity on silica stationary phase can be calculated using RM values, similar to the lipophilicity indices.

Original languageEnglish
Pages (from-to)2337-2344
Number of pages8
JournalJournal of Liquid Chromatography and Related Technologies
Volume30
Issue number15
DOIs
Publication statusPublished - Sep 1 2007

Keywords

  • Hydrophylicity
  • Pyridinium aldoximes
  • R values
  • Silica
  • TLC

ASJC Scopus subject areas

  • Analytical Chemistry
  • Biochemistry
  • Pharmaceutical Science
  • Clinical Biochemistry

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