2012
DOI: 10.1016/j.jcis.2012.02.016
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Solubilization of two organic dyes by cationic ester-containing gemini surfactants

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Cited by 102 publications
(65 citation statements)
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“…Comprehensive experimental systematic studies of the solubilization of long-chain hydrophobic components by gemini surfactant micelles are, unfortunately, still missing and experimental evidence of the role of spacer group length is, to our knowledge, not yet available. [43][44][45][46][47] …”
Section: Influence Of Bending Elasticity Constants On Solubilizatimentioning
confidence: 99%
“…Comprehensive experimental systematic studies of the solubilization of long-chain hydrophobic components by gemini surfactant micelles are, unfortunately, still missing and experimental evidence of the role of spacer group length is, to our knowledge, not yet available. [43][44][45][46][47] …”
Section: Influence Of Bending Elasticity Constants On Solubilizatimentioning
confidence: 99%
“…cmc of gemini surfactants being 10 to 100-times smaller than that of conventional single-chain surfactants, results in much less skin irritation which allows to use them as skin permeation enhancers [18]. A smaller value of their cmc also enables them to be efficient solubilisers of low soluble drugs [19], dyes [20,21], hydrocarbons such as n-hexane and toluene [22]. Gemini surfactants can also serve as structural units in the formulation of cationic liposomes [23].…”
Section: Introductionmentioning
confidence: 99%
“…These properties make gemini surfactants of special interest for biological and biomedical applications. Gemini surfactants appear to be adequate drug carriers due to their much lower CMC values and higher solubilization capacities compared with those of the corresponding monomeric surfactants [7][8][9][10]. These characteristics suggest that gemini surfactants with a degradable or stimuli-sensitive spacer can form micelles for controlled drug release.…”
Section: Introductionmentioning
confidence: 99%