Volumetric studies of aqueous solutions of local anesthetical drug compounds [hydrochlorides of procaine (PC HCl), lidocaine (LC HCl) and tetracaine (TC HCl)] at 298.15 K

被引:36
|
作者
Shaikh, Vasim R. [1 ]
Dagade, Dilip H. [2 ]
Hundiwale, Dilip G. [1 ]
Patil, Kesharsingh J. [1 ]
机构
[1] N Maharashtra Univ, Sch Chem Sci, Jalgaon 425001, India
[2] Shivaji Univ, Dept Chem, Kolhapur 416004, Maharashtra, India
关键词
Aqueous solution; Anesthetical drug molecule; Partial molar volume; Aggregation; Micelle formation; APPARENT MOLAL VOLUMES; THERMODYNAMIC PROPERTIES; ADIABATIC COMPRESSIBILITY; SODIUM DECANOATE; WATER; TEMPERATURE; MODEL; DEPENDENCE; BEHAVIOR; DESIGN;
D O I
10.1016/j.molliq.2011.09.024
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
In order to probe micellization phenomenon and structural interactions in aqueous solutions of local anesthetical drug compounds procaine hydrochloride (PC HCl), lidocaine hydrochloride (LC HCl) and tetracaine hydrochloride (TC HCl), we carried out experimental measurement of densities as a function of drug concentration at 298.15 K. The derived properties like apparent molar volumes (phi(V)) and partial molar volume ((V) over bar (2)) of the drug molecules were appropriately calculated, treating drug molecules as electrolytes. The limiting partial molar volumes ((F) over bar (0)(2)), critical micelle concentrations (cmc) and aggregation number (n) are estimated and found to be 225.00.10(3) mm(3)mol(-1), 0.45 mol kg(-1) and 2 for PC HCl, 237.10.10(3) mm(3)mol(-1), 0.13 mol kg(-1) and 8 for LC HCl and 259.80.10(3) mm(3)mol(-1), 0.17 mol kg(-1) and 6 for TC HCl respectively. Applying the pseudo-phase separation model the volume changes due to micellization (Delta V(x)(m)) are estimated and are found to be 0.37.10(3) mm(3)mol(-1).17.10(3) mm(3)mol(-1) and 1.50.10(3) mm(3)mol(-1) for PC HCl, LC HCl and TC HCl respectively. These results are explained on the basis of drug-water interactions and hydrophobic interactions (i.e. solute-solute interaction) which seem to depend upon the structural characteristic of the linkages involved and difference in the chain which binds the hydrophobic group and hydrophilic group in the studied drug molecules. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 242
页数:4
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