2019
DOI: 10.1016/j.molliq.2018.12.006
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Aggregation behaviour of tetracaine hydrochloride with Gemini surfactants and the formation of silver nanoparticles using drug-Gemini surfactants mixture

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Cited by 30 publications
(10 citation statements)
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“…Such a combination helps us to monitor both hydrophilic (between anionic SDS and cationic Gemini) and hydrophobic (due to hydrocarbon chains) interactions operating between the surfactant molecules adsorbed on Au and Ag NPs. A Gemini surfactant is made up of two identical monomeric homologues connected usually at the level of the dimeric head group. This unique molecular structure provides a Gemini surfactant with double hydrocarbon chains and double polar head groups with a much stronger ability to undergo both hydrophobic and hydrophilic interactions in comparison to their conventional monomeric homologues. The amphipathic nature of Gemini surfactants also mimics several complex biological molecules such as phospholipids and biological surfactants. Thus, NP surface-adsorbed Gemini surfactant systems can be treated as models for bio-nanomaterials in biological applications.…”
Section: Introductionmentioning
confidence: 99%
“…Such a combination helps us to monitor both hydrophilic (between anionic SDS and cationic Gemini) and hydrophobic (due to hydrocarbon chains) interactions operating between the surfactant molecules adsorbed on Au and Ag NPs. A Gemini surfactant is made up of two identical monomeric homologues connected usually at the level of the dimeric head group. This unique molecular structure provides a Gemini surfactant with double hydrocarbon chains and double polar head groups with a much stronger ability to undergo both hydrophobic and hydrophilic interactions in comparison to their conventional monomeric homologues. The amphipathic nature of Gemini surfactants also mimics several complex biological molecules such as phospholipids and biological surfactants. Thus, NP surface-adsorbed Gemini surfactant systems can be treated as models for bio-nanomaterials in biological applications.…”
Section: Introductionmentioning
confidence: 99%
“…A lot of work has been done to improve the problem associated with stability and biocompatibility of poorly soluble drugs [3][4][5][6][7][8]. There have been a very few strategies developed for improving the solubility of poorly soluble drugs which include their complexation with other surface-active substances like conventional surfactants, gemini surfactants and ionic liquids [5,[9][10][11][12]. To lower the hydrophobicity and increasing hydrophilicity of poorly soluble drugs, alternative solvents like ILs have been used.…”
Section: Introductionmentioning
confidence: 99%
“…TCH is also available in combination with lidocaine that is used as a local anesthetic cream. In surgery or other similar procedure, TCH blocks the pain signals by nerve endings [ 11 , 12 ]. The interaction between the anesthetic molecule and lipid molecules of the biomembrane at the interface is responsible for the anesthetic action of the drug.…”
Section: Introductionmentioning
confidence: 99%