Literature DB >> 26485055

The potential of immobilized artificial membrane chromatography to predict human oral absorption.

Fotios Tsopelas1, Theodosia Vallianatou2, Anna Tsantili-Kakoulidou2.   

Abstract

The potential of immobilized artificial membrane (IAM) chromatography to estimate human oral absorption (%HOA) was investigated. For this purpose, retention indices on IAM stationary phases reported previously by our group or measured by other authors under similar conditions were used to model %HOA data, compiled from literature sources. Considering the pH gradient in gastrointestinal tract, the highest logkw(IAM) values were considered, obtained either at pH7.4 or 5.5, defined as logkw(IAM)(best). Non linear models were established upon introduction of additional parameters and after exclusion of drugs which are substrates either to efflux or uptake transporters. The best model included Abraham's hydrogen-bond acidity parameter, molecular weight as well as the positively and negatively charged molecular fractions. For reasons of comparison between IAM chromatography and traditional lipophilicity, corresponding models were derived by replacing IAM retention factors with octanol-water distribution coefficients (logD). An overexpression of electrostatic interactions with phosphate anions was observed in the case of IAM retention as expressed by the negative contribution of the positively charged fraction F(+). The same parameter is statistically significant also in the logD model, but with a positive sign, indicating the attraction of basic drugs in the negatively charged inner membrane. To validate the obtained models a blind test set of 22 structurally diverse drugs was used, whose logkw(IAM)(best) values were determined and analyzed in the present study under similar conditions. IAM retention factors were further compared with MDCK cell lines permeability data taken from literature for a set of validation drugs. The overexpression of electrostatic interactions with phosphate anions on IAM surface was also evident in respect to MDCK permeability. In contrast to the clear classification between drugs with high and poor (or intermediate) absorption provided by MDCK permeability, %HOA plotted versus both IAM and logD data result in a saturation curve with a smoother ascending line.
Copyright © 2015 Elsevier B.V. All rights reserved.

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Keywords:  Electrostatic interactions; Human oral absorption; IAM.PC.DD2; Immobilized artificial membrane chromatography; Lornoxicam (PubChem CID: 54690031); MDCK; Meloxicam (PubChem CID: 54677470); Methylprednisolone (PubChem CID: 6741); Metoclopramide (PubChem CID: 4168); Minoxidil (PubChem CID: 4201); Nadolol (PubChem CID: 39147); Niflumic acid (PubChem CID: 4488); Octanol–water partitioning; Omeprazole (PubChem CID: 4594); Sulpiride (PubChem CID: 5355); Warfarin (PubChem CID: 54678486)

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Year:  2015        PMID: 26485055     DOI: 10.1016/j.ejps.2015.09.020

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  6 in total

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Journal:  Molecules       Date:  2017-10-28       Impact factor: 4.411

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Journal:  Molecules       Date:  2019-10-21       Impact factor: 4.411

4.  Pharmacokinetic Profiling and Simultaneous Determination of Thiopurine Immunosuppressants and Folic Acid by Chromatographic Methods.

Authors:  Edvin Brusač; Mario-Livio Jeličić; Daniela Amidžić Klarić; Biljana Nigović; Nikša Turk; Ilija Klarić; Ana Mornar
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5.  Revisiting the application of Immobilized Artificial Membrane (IAM) chromatography to estimate in vivo distribution properties of drug discovery compounds based on the model of marketed drugs.

Authors:  Klara Valko; Silvia Rava; Shenaz Bunally; Scott Anderson
Journal:  ADMET DMPK       Date:  2020-01-31

6.  Prediction Models for Brain Distribution of Drugs Based on Biomimetic Chromatographic Data.

Authors:  Theodosia Vallianatou; Fotios Tsopelas; Anna Tsantili-Kakoulidou
Journal:  Molecules       Date:  2022-06-07       Impact factor: 4.927

  6 in total

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