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Polyethylene glycol-stabilized lipid disks as model membranes in interaction studies based on electrokinetic capillary chromatography and quartz crystal microbalance
University Helsinki, Finland.
Uppsala University, Sweden.
University Helsinki, Finland.
Karlstad University, Faculty of Health, Science and Technology (starting 2013), Department of Engineering and Chemical Sciences. (INTERACT)ORCID iD: 0000-0003-1819-1709
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2011 (English)In: Analytical Biochemistry, ISSN 0003-2697, E-ISSN 1096-0309, Vol. 414, no 1, 117-124 p.Article in journal (Refereed) Published
Abstract [en]

Distearoylphosphatidylcholine (DSPC)/cholesterol/distearoylphosphatidylethanolamine (DSPE)-polyethylene glycol 5000 [PEG(5000)] lipid disks, mimicking biological membranes, were used as pseudostationary phase in partial filling electrokinetic capillary chromatography (EKC) to study interactions between pharmaceuticals and lipid disks. Capillaries were coated either noncovalently with a poly(1-vinylpyrrolidone)-based copolymer or covalently with polyacrylamide to mask the negative charges of the fused-silica capillary wall and to minimize interactions between positively charged pharmaceuticals and capillary wall. Although the noncovalent copolymer coating method was faster, better stability of the covalent polyacrylamide coating at physiological pH 7.4 made it more reliable in partial filling EKC studies. Migration times of pharmaceuticals were proportional to the amount of lipids in the pseudostationary phase, and partition coefficients were successfully determined. Because the capillary coatings almost totally suppressed the electroosmotic flow, it was not practical to use the EKC-based method for partition studies involving large molecules with low mobilities. Hence, the applicability of the biomembrane mimicking lipid disks for interactions studies with large molecules was verified by the quartz crystal microbalance technique. Biotinylated lipid disks were then immobilized on streptavidincoated sensor chip surface, and interactions with a high-molecular-mass molecule, lysozyme, were studied. Cryo-transmission electron microscopy and asymmetrical flow field-flow fractionation were used to clarify the sizes of lipid disks used. (C) 2011 Elsevier Inc. All rights reserved.

Place, publisher, year, edition, pages
Elsevier, 2011. Vol. 414, no 1, 117-124 p.
Keyword [en]
Electrokinetic capillary chromatography, Partial filling technique, Bilayer disks, Pharmaceuticals, Partition coefficient
National Category
Polymer Chemistry
Identifiers
URN: urn:nbn:se:kau:diva-46873DOI: 10.1016/j.ab.2011.03.016ISI: 000290704300016PubMedID: 21419750OAI: oai:DiVA.org:kau-46873DiVA: diva2:1037514
Available from: 2016-10-16 Created: 2016-10-16 Last updated: 2016-10-20Bibliographically approved

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