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Lateral Diffusion Rates of Lipid, Water, and a Hydrophobic Drug in a Multilamellar Liposome

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2003 Aug 29
PMID 12944288
Citations 40
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Abstract

The lateral diffusion constants of 1-palmitoyl-2-oleoyl-sn-glycero-3 phosphocholine (POPC), water, and ibuprofen were measured in multilamellar liposomes using pulsed field gradient magic-angle spinning (PFG-MAS) (1)H NMR. The analysis of diffusion data obtained in powder samples and a method for liposome curvature correction are presented. At 322 K POPC has a diffusion constant of (8.6 +/- 0.2) x 10(-12) m(2)/s when dehydrated (8.2 waters/lipid) and (1.9 +/- 0.1) x 10(-11) m(2)/s in excess water. The diffusion constant of water in dehydrated POPC was found to be (4.7 +/- 0.1) x 10(-10) m(2)/s. The radius of curvature is 21 +/- 2 microm for the dehydrated sample and 4.5 +/- 0.5 microm for POPC sample containing excess water. The activation energies of diffusion are 40.6 +/- 0.4 kJ/mole for dehydrated POPC, 30.7 +/- 0.9 kJ/mole for POPC with excess water, and 28.6 +/- 1.5 kJ/mole for water in dehydrated POPC. The diffusion constants and activation energies for a sample of POPC/ibuprofen/water (1:0.56:15) were also measured. The ibuprofen, which locates in the lipid-water interface, diffuses faster than POPC but has a slightly higher activation energy of lateral diffusion. Within certain restrictions, PFG-MAS NMR provides a useful method for characterizing membrane organization and mobility.

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References
1.
Mason R, Rhodes D, Herbette L . Reevaluating equilibrium and kinetic binding parameters for lipophilic drugs based on a structural model for drug interaction with biological membranes. J Med Chem. 1991; 34(3):869-77. DOI: 10.1021/jm00107a001. View

2.
Brumm T, Mops A, Dolainsky C, Bruckner S, Bayerl T . Macroscopic orientation effects in broadline NMR-spectra of model membranes at high magnetic field strength: A method preventing such effects. Biophys J. 2009; 61(4):1018-24. PMC: 1260361. DOI: 10.1016/S0006-3495(92)81909-4. View

3.
LINDBLOM G, Wennerstrom H . Amphiphile diffusion in model membrane systems studied by pulsed NMR. Biophys Chem. 1977; 6(2):167-71. DOI: 10.1016/0301-4622(77)87006-3. View

4.
Koenig B, Strey H, Gawrisch K . Membrane lateral compressibility determined by NMR and x-ray diffraction: effect of acyl chain polyunsaturation. Biophys J. 1997; 73(4):1954-66. PMC: 1181096. DOI: 10.1016/S0006-3495(97)78226-2. View

5.
Mair R, Rosen M, Wang R, Cory D, Walsworth R . Diffusion NMR methods applied to xenon gas for materials study. Magn Reson Chem. 2003; 40(13):S29-39. DOI: 10.1002/mrc.1114. View