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Evaluating the Potential of Cubosomal Nanoparticles for Oral Delivery of Amphotericin B in Treating Fungal Infection

Overview
Publisher Dove Medical Press
Specialty Biotechnology
Date 2014 Jan 15
PMID 24421641
Citations 21
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Abstract

The oral administration of amphotericin B (AmB) has a major drawback of poor bioavailability. The aim of this study was to investigate the potential of glyceryl monoolein (GMO) cubosomes as lipid nanocarriers to improve the oral efficacy of AmB. Antifungal efficacy was determined in vivo in rats after oral administration, to investigate its therapeutic use. The human colon adenocarcinoma cell line (Caco-2) was used in vitro to evaluate transport across a model of the intestinal barrier. In vivo antifungal results showed that AmB, loaded in GMO cubosomes, could significantly enhance oral efficacy, compared against Fungizone, and that during a 2 day course of dosage 10 mg/kg the drug reached effective therapeutic concentrations in renal tissue for treating fungal infections. In the Caco-2 transport studies, GMO cubosomes resulted in a significantly larger amount of AmB being transported into Caco-2 cells, via both clathrin- and caveolae-mediated endocytosis, but not macropinocytosis. These results suggest that GMO cubosomes, as lipid nanovectors, could facilitate the oral delivery of AmB.

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References
1.
Li N, Li X, Zhou Y, Li W, Zhao Y, Ma S . The use of polyion complex micelles to enhance the oral delivery of salmon calcitonin and transport mechanism across the intestinal epithelial barrier. Biomaterials. 2012; 33(34):8881-92. DOI: 10.1016/j.biomaterials.2012.08.047. View

2.
Vertzoni M, Markopoulos C, Symillides M, Goumas C, Imanidis G, Reppas C . Luminal lipid phases after administration of a triglyceride solution of danazol in the fed state and their contribution to the flux of danazol across Caco-2 cell monolayers. Mol Pharm. 2012; 9(5):1189-98. DOI: 10.1021/mp200479f. View

3.
Wasan E, Bartlett K, Gershkovich P, Sivak O, Banno B, Wong Z . Development and characterization of oral lipid-based amphotericin B formulations with enhanced drug solubility, stability and antifungal activity in rats infected with Aspergillus fumigatus or Candida albicans. Int J Pharm. 2009; 372(1-2):76-84. DOI: 10.1016/j.ijpharm.2009.01.003. View

4.
Roger E, Lagarce F, Garcion E, Benoit J . Lipid nanocarriers improve paclitaxel transport throughout human intestinal epithelial cells by using vesicle-mediated transcytosis. J Control Release. 2009; 140(2):174-81. DOI: 10.1016/j.jconrel.2009.08.010. View

5.
Risovic V, Sachs-Barrable K, Boyd M, Wasan K . Potential mechanisms by which Peceol increases the gastrointestinal absorption of amphotericin B. Drug Dev Ind Pharm. 2004; 30(7):767-74. DOI: 10.1081/ddc-120039793. View