| Literature DB >> 18271034 |
Megan Tufteland1, Gang Ren, Robert O Ryan.
Abstract
The goal of this study was to determine the effect of apolipoproteins on Amphotericin B lipid complex (ABLC). We report that incubation of ABLC with recombinant human apolipoprotein A-I (apoA-I) induces solubilization of ABLC by transforming the micron sized phospholipid/AMB assemblies into discrete nanoscale disk-shaped complexes termed nanodisks (ND). ApoA-I induced changes in ABLC solubility and morphology were monitored by spectroscopy and electron microscopy. AMB efficacy was evaluated in yeast and pathogenic fungi growth inhibition assays and the effect of AMB formulation on cell toxicity was assessed in cultured Hep3B cells. AMB associated with ND were more efficiently nebulized than AMB associated with ABLC. Thus, transformation of ABLC into ND preserves the potent biological activity of AMB as well as the reduced toxicity of the ABLC formulation. ABLC derived AMB-ND offer advantages over conventional ABLC in terms of stability, storage, nebulization efficiency and provides an intrinsic "handle" for tissue specific targeting via genetic engineering of its protein component. (c) 2008 Wiley-Liss, Inc. and the American Pharmacists AssociationEntities:
Mesh:
Substances:
Year: 2008 PMID: 18271034 PMCID: PMC2893587 DOI: 10.1002/jps.21325
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534