Literature DB >> 19432455

Biophysical interactions with model lipid membranes: applications in drug discovery and drug delivery.

Chiranjeevi Peetla1, Andrew Stine, Vinod Labhasetwar.   

Abstract

The transport of drugs or drug delivery systems across the cell membrane is a complex biological process, often difficult to understand because of its dynamic nature. In this regard, model lipid membranes, which mimic many aspects of cell-membrane lipids, have been very useful in helping investigators to discern the roles of lipids in cellular interactions. One can use drug-lipid interactions to predict pharmacokinetic properties of drugs, such as their transport, biodistribution, accumulation, and hence efficacy. These interactions can also be used to study the mechanisms of transport, based on the structure and hydrophilicity/hydrophobicity of drug molecules. In recent years, model lipid membranes have also been explored to understand their mechanisms of interactions with peptides, polymers, and nanocarriers. These interaction studies can be used to design and develop efficient drug delivery systems. Changes in the lipid composition of cells and tissue in certain disease conditions may alter biophysical interactions, which could be explored to develop target-specific drugs and drug delivery systems. In this review, we discuss different model membranes, drug-lipid interactions and their significance, studies of model membrane interactions with nanocarriers, and how biophysical interaction studies with lipid model membranes could play an important role in drug discovery and drug delivery.

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Year:  2009        PMID: 19432455      PMCID: PMC2757518          DOI: 10.1021/mp9000662

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  87 in total

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4.  Structure of a gel phase lipid bilayer prepared by the Langmuir-Blodgett/Langmuir-Schaefer method characterized by sum-frequency vibrational spectroscopy.

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5.  Interaction of the macrolide antibiotic azithromycin with lipid bilayers: effect on membrane organization, fluidity, and permeability.

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9.  Probing chitosan and phospholipid interactions using Langmuir and Langmuir-Blodgett films as cell membrane models.

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  74 in total

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5.  Turbidity spectroscopy for characterization of submicroscopic drug carriers, such as nanoparticles and lipid vesicles: size determination.

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Review 6.  Peptoid drug discovery and optimization via surface X-ray scattering.

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7.  Scaling and alpha-helix regulation of protein relaxation in a lipid bilayer.

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8.  Kinematics, material symmetry, and energy densities for lipid bilayers with spontaneous curvature.

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9.  Profiling lipid-protein interactions using nonquenched fluorescent liposomal nanovesicles and proteome microarrays.

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10.  Selective biophysical interactions of surface modified nanoparticles with cancer cell lipids improve tumor targeting and gene therapy.

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