Literature DB >> 8673230

Immobilized-artificial-membrane chromatography: measurements of membrane partition coefficient and predicting drug membrane permeability.

S Ong1, H Liu, C Pidgeon.   

Abstract

Immobilized artificial membranes (IAMs) are chromatographic surfaces prepared by covalently immobilizing cell membrane phospholipids to solid surfaces at monolayer densities. IAM surfaces mimic fluid cell membranes. For 23 structurally unrelated compounds, solute capacity factors [log (k'IAM)] measured on IAM columns correlate very well with the solute equilibrium partition coefficients [log (Km)] measured in fluid liposome systems (r = 0.907). This indicates that solute partitioning between the IAM bonded phase and the aqueous mobile phase is similar to the solute partitioning between liposomes and the aqueous phase. IAMs also predicted oral drug absorption in mice and drug permeability through Caco-2 cells. IAM chromatography is experimentally simple and large volume screening of experimental compounds for drug absorption is possible. Solute retention on IAMs was found to be dominated by a partitioning mechanism. The structural requirements for HPLC bonded phases to predict solute-membrane partitioning are briefly discussed.

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Year:  1996        PMID: 8673230     DOI: 10.1016/0021-9673(95)00837-3

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  24 in total

1.  Molecular factors influencing retention on immobilized artifical membranes (IAM) compared to partitioning in liposomes and n-octanol.

Authors:  Agnes Taillardat-Bertschinger; Catherine A Marca Martinet; Pierre-Alain Carrupt; Marianne Reist; Giulia Caron; Roberta Fruttero; Bernard Testa
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Review 2.  Lipophilicity and its relationship with passive drug permeation.

Authors:  Xiangli Liu; Bernard Testa; Alfred Fahr
Journal:  Pharm Res       Date:  2010-10-30       Impact factor: 4.200

3.  The role of lipophilicity in determining binding affinity and functional activity for 5-HT2A receptor ligands.

Authors:  Matthew A Parker; Deborah M Kurrasch; David E Nichols
Journal:  Bioorg Med Chem       Date:  2008-02-14       Impact factor: 3.641

Review 4.  Modeling kinetics of subcellular disposition of chemicals.

Authors:  Stefan Balaz
Journal:  Chem Rev       Date:  2009-05       Impact factor: 60.622

5.  Effects on membrane lateral pressure suggest permeation mechanisms for bacterial quorum signaling molecules.

Authors:  Kishore Kamaraju; Jacqueline Smith; Jingxin Wang; Varnika Roy; Herman O Sintim; William E Bentley; Sergei Sukharev
Journal:  Biochemistry       Date:  2011-07-21       Impact factor: 3.162

6.  A method to predict blood-brain barrier permeability of drug-like compounds using molecular dynamics simulations.

Authors:  Timothy S Carpenter; Daniel A Kirshner; Edmond Y Lau; Sergio E Wong; Jerome P Nilmeier; Felice C Lightstone
Journal:  Biophys J       Date:  2014-08-05       Impact factor: 4.033

7.  Drug-membrane interactions studied in phospholipid monolayers adsorbed on nonporous alkylated microspheres.

Authors:  Viera Lukacova; Ming Peng; Gail Fanucci; Roman Tandlich; Anne Hinderliter; Bikash Maity; Ethirajan Manivannan; Gregory R Cook; Stefan Balaz
Journal:  J Biomol Screen       Date:  2007-01-11

8.  Odyssey of a cancer nanoparticle: from injection site to site of action.

Authors:  Joseph W Nichols; You Han Bae
Journal:  Nano Today       Date:  2012-12-01       Impact factor: 20.722

Review 9.  In vitro cerebrovascular modeling in the 21st century: current and prospective technologies.

Authors:  Christopher A Palmiotti; Shikha Prasad; Pooja Naik; Kaisar M D Abul; Ravi K Sajja; Anilkumar H Achyuta; Luca Cucullo
Journal:  Pharm Res       Date:  2014-08-07       Impact factor: 4.200

10.  Exploratory neuropharmacological evaluation of a conformationally constrained thyrotropin-releasing hormone analogue.

Authors:  Meritxell Teixidó; Katalin Prokai-Tatrai; Xiaoli Wang; Vien Nguyen; Laszlo Prokai
Journal:  Brain Res Bull       Date:  2007-03-15       Impact factor: 4.077

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