N.S. Kurnakov Institute of General and Inorganic Chemistry of Russian Academy of Sciences, Leninskii pr.31, Moscow, 119991, Russia.
N.S. Kurnakov Institute of General and Inorganic Chemistry of Russian Academy of Sciences, Leninskii pr.31, Moscow, 119991, Russia.
Talanta. 2022 May 1;241:123239. doi: 10.1016/j.talanta.2022.123239. Epub 2022 Jan 25.
The detection of local anesthetic drugs is of great importance in the analysis of pharmaceutical, clinical and forensic samples. This paper reports a simple and sensitive potentiometric assay suitable for detecting general local anesthetics (LAs) of two types, namely: amino ester-anesthetics (procaine) and amino amide-anesthetics (lidocaine, articaine). As a detector, a new highly sensitive sensor based on a poly(vinyl chloride)-matrix membrane incorporating ion-pair complexes of protonated procaine with 2-[bis-octadecyl-sulfonic)-closo-decaborate is used. To improve the analytical characteristics of the sensor, the tetradodecylammonium - 2-[bis-octadecyl-sulfonic)-closo-decaborate associate as a lipophilic additive is proposed. The procedures for the synthesis of both electroactive membrane components are described. The dependence of potential response characteristics of the potentiometric system on the membrane composition, local anesthetic properties, and pH of the sample solutions is discussed. The difference in sensitivity and selectivity of the sensor was found to be responsible for the lipophilic property and pK values of local anesthetic molecules. The developed sensor exhibited a near Nernstian response to cationic forms of procaine and some other anesthetics of higher lipophility, in particular lidocaine and articaine, over a wide linear concentration range. The limit of detection was varied from 2 × 10 to 5 × 10 μM, and it is the lowest value among the early published potentiometric analogs. The proposed method was successfully applied to the analysis of pharmaceutical formulations and spiked enzyme-free urine samples containing LAs at low concentration levels (0.5-100 μg mL). The recovery range (n = 5) was 98.0-101.5%, and the relative standard deviation was no more than 5.0%.
局部麻醉剂的检测在药物分析、临床和法医样本分析中非常重要。本文报道了一种简单灵敏的电位测定法,适用于检测两种类型的一般局部麻醉剂(LAs):氨基酯类麻醉剂(普鲁卡因)和氨基酰胺类麻醉剂(利多卡因、阿替卡因)。作为检测器,使用了一种基于聚氯乙烯基质膜的新型高灵敏度传感器,该传感器包含质子化普鲁卡因与 2-[双-(十八烷基)-磺酸)-closo-癸硼酸盐的离子对复合物。为了提高传感器的分析特性,提出了将四癸基铵-2-[双-(十八烷基)-磺酸)-closo-癸硼酸盐缔合物作为亲脂性添加剂。描述了两种电活性膜成分的合成过程。讨论了电位系统的电位响应特性与膜组成、局部麻醉剂性质和样品溶液 pH 值的关系。发现传感器的灵敏度和选择性的差异归因于局部麻醉剂分子的亲脂性和 pK 值。开发的传感器对阳离子形式的普鲁卡因和其他一些亲脂性更高的麻醉剂(特别是利多卡因和阿替卡因)表现出近 Nernstian 响应,在宽线性浓度范围内。检测限变化范围为 2×10 至 5×10μM,这是早期发表的电位类似物中最低的值。该方法成功应用于含有低浓度局部麻醉剂(0.5-100μgmL)的药物制剂和未经酶处理的尿液样品的分析。回收率范围(n=5)为 98.0-101.5%,相对标准偏差不超过 5.0%。