2009
DOI: 10.1016/j.colsurfb.2009.03.029
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Solubilization of resveratrol in micellar solutions of different bile acids

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Cited by 66 publications
(38 citation statements)
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“…According to the ratios of the three biliary lipids, different topologies may form and vary in particle size ranging from simple micelles (1-2 nm) to MM (4-10 nm), small unilamellar vesicles (40-100 nm) and, finally, large multilamellar vesicles (300-500 nm). 11,53 Endogenous self-assembled aggregates of bile lipids were exploited by pharmaceutical researchers to fabricate BS-integrated nanocarriers, as will be discussed in the following section. …”
Section: Peculiar Structure and Self-assembled Topologiesmentioning
confidence: 99%
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“…According to the ratios of the three biliary lipids, different topologies may form and vary in particle size ranging from simple micelles (1-2 nm) to MM (4-10 nm), small unilamellar vesicles (40-100 nm) and, finally, large multilamellar vesicles (300-500 nm). 11,53 Endogenous self-assembled aggregates of bile lipids were exploited by pharmaceutical researchers to fabricate BS-integrated nanocarriers, as will be discussed in the following section. …”
Section: Peculiar Structure and Self-assembled Topologiesmentioning
confidence: 99%
“…11,44,48 Nevertheless, a contradictory effect was demonstrated when exogenous bile was coadministered with oral solid formulations. 91 Administration of exogenous bile was accompanied by decreased oral bioavailability of atenolol 95 and nitrendipine.…”
Section: Paradoxical Effects Of Bsmentioning
confidence: 99%
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“…Micellar solutions of bile acids allow the solubilization of poorly soluble organic substances and can improve their resorption, as these micelles are composed of bile acids, which represent bi-planar biological surfactants, with two functionally different molecular surfaces: a hydrophobic convex surface of steroid core, and a hydrophilic concave surface, representing amphiphilic molecules (Atanacković et al, 2009;Atanacković, Gojković-Bukarica, Cvejić, 2012). Furthermore, these compounds have been studied as permeability enhancers of biological membranes, such as the skin barrier, as above their critical micellar concentration (CMC), they can associate with cell membrane phospholipids and cause interruption of membrane integrity.…”
Section: Micellar Systemsmentioning
confidence: 99%
“…This coexistence of non-polar and polar surfaces influences their physico-chemical properties [1][2][3][4] such as formation of self-association micelles that have significant role in the physiology of the metabolism of fats, absorption of liposoluble vitamins and hydrophobic drugs. Beside their physiological role, micellar solutions of bile acids can solubilizate poorly soluble organic substances [5]. Furthermore, bile acids have a promoting effect in the transport of some polar drugs [6].…”
Section: Introductionmentioning
confidence: 99%