Binding interactions of anesthetic drug with surface active ionic liquid

被引:43
|
作者
Pal, Amalendu [1 ]
Yadav, Alka [1 ]
机构
[1] Kurukshetra Univ, Dept Chem, Kurukshetra 136119, Haryana, India
关键词
Ionic liquids; Lidocaine hydrochloride; Conductance; Surface tension; Fluorescence; AGGREGATION BEHAVIOR; MICELLE FORMATION; DELIVERY; MICELLIZATION; LIDOCAINE; SYSTEMS; ABILITY;
D O I
10.1016/j.molliq.2016.07.076
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The application of aggregation behavior of a surface active ionic liquids (SAILs), 1-dodecy1-3-methylimidazolium chloride (C(12)mim][Cl] and 1-tetradecy1-3-methylimidazolium chloride [C(14)mim][Cl] in drug delivery of lidocaine hydrochloride has been investigated from surface tension and fluorescence measurements at 298.15 K and from conductance at 288.15, 298.15 and 308.15 K. Critical aggregation concentration (CAC), degree of ionization (alpha), and various thermodynamic parameters like Gibbs free energy of aggregation (Delta G(agg)degrees) standard enthalpy of aggregation (Delta H-agg degrees) and standard entropy of aggregation (Delta S-agg degrees) are calculated using conductivity measurements. The surface activity of the Its in various mixed solvents are examined from surface tension measurements by calculating various surface parameters like maximum surface excess concentration (Gamma(max)), minimum surface area per ionic liquid molecule (A(min)), adsorption efficiency (pC(20)), effectiveness of surface tension reduction (Pi(cac)) surface tension at CAC (gamma(cac)), p (packing parameter), and CAC at different compositions. Fluorescence measurements, have been employed to get detailed insight of the local microenvironment of the aggregates, and critical aggregation concentration (CAC). Decrease in the CAC values was observed with the increase in the amount of drug which is attributed to the balancing between electrostatic and hydrophobic interactions. This shows that the spontaneity of aggregation process of IL increases with the increase in the concentration of drug. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:471 / 479
页数:9
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