Improved Chromatographic Bioavailability Estimations.

Abstract

The question of how to assess bioavailability has received much attention. Bioavailabilty is most often approximated by the distribution of the solute in question between two phases, most often bulk phases, of water and an immiscible organic solvent. Since the inception of reversed phase liquid chromatography there have been many attempts to correlate chromatographic retention with bioavailability and the most often used bulk measure, the octanol-water partition coefficient. An entire field has developed around this research, referred to as Quantitative Structure Activity Relationships (QSAR), or where chromatographic retention is the measured parameter, Quantitative Structure Retention Relationships (QSRR). Yet with present technology, these attempts are inevitably doomed to failure. On the one hand, bulk phases are not appropriate for modeling a partitioning process in an interphase such as biological membranes, and while chromatographic stationary phases can be argued as having similar structure to a membrane because of chain organization, the density of the grafted chains is much too low to provide a suitable model. It is these problems which we have come to understand and propose to address.

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 1996
Accession Number
ADA326171

Entities

People

  • John G. Dorsey

Organizations

  • Florida State University

Tags

Communities of Interest

  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Alcohols
  • Capillary Electrophoresis
  • Chemical Synthesis
  • Chemistry
  • Cholesterol
  • Chromatography
  • Coefficients
  • High Density
  • Liquid Chromatography
  • Membrane Lipids
  • Membranes
  • Organic Solvents
  • Phase Transformations
  • Raman Spectroscopy
  • Solvents
  • Stationary

Readers

  • Agricultural Chemistry/Soil Science
  • Molecular and Cellular Biochemistry
  • Theoretical Analysis.