Oertel R, Richter K, Weile K, Gramatté T, Berndt A, Feller K
Institute of Clinical Pharmacology, Medical Academy C.G. Carus, Dresden, FRG.
Methods Find Exp Clin Pharmacol. 1993 Oct;15(8):541-7.
This study was undertaken to develop a time- and cost-effective method for the detection of articaine and articainic acid in alveolus blood by high-performance liquid chromatography with a simple method of sample pretreatment. To overcome the problem of very rapid hydrolysis a method for controlling hydrolysis in vitro after blood sampling was developed. Blood samples were withdrawn from the alveolus of the upper molars 2-14 min after submucous injection of articaine (2.0 ml 4%) or identical injection of lidocaine (2.0 ml 2%). The higher blood levels found for articaine correspond to the higher concentration of the drug in the injection solution. A relationship between the serum concentration of articaine and lidocaine, respectively, and the time between injection and blood sampling could be established.
本研究旨在开发一种高效液相色谱法,通过简单的样品预处理方法,实现对牙槽血中阿替卡因和阿替卡因酸的检测,该方法具有时间和成本效益。为克服阿替卡因快速水解的问题,开发了一种采血后体外控制水解的方法。在黏膜下注射阿替卡因(2.0 ml 4%)或相同剂量的利多卡因(2.0 ml 2%)后2 - 14分钟,从右上磨牙牙槽抽取血样。阿替卡因的血药浓度较高,这与注射溶液中药物的较高浓度相对应。分别建立了阿替卡因和利多卡因血清浓度与注射和采血之间时间的关系。