Tanaka Einosuke, Nakamura Takako, Inomata Shinichi, Honda Katsuya
Institute of Community Medicine, University of Tsukuba, Ibaraki-ken 305-8575, Japan.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Apr 13;834(1-2):213-6. doi: 10.1016/j.jchromb.2006.02.034. Epub 2006 Mar 9.
A high-performance liquid chromatographic (HPLC) method has been developed for the simultaneous analysis of the local anesthetic amide drugs, bupivacaine, mepivacaine and ropivacaine, belonging to the pipecoloxylidide group using a C(18) reversed-phase column (150 x 4.6 mm I.D.) filled with 5-microm particles and attached to a UV detector. The mobile phase was composed of acetonitrile-methanol-30 mM NaH(2)PO(4) (pH 5.6) (100:100:300, v/v/v) and the flow rate was 1ml/min. The absorbance of the eluate was monitored at 210 nm. The retention times of the three compounds were: 4.6 min (mepivacaine), 9.7min (ropivacaine) and 16.4 min (bupivacaine). With this sample preparation method, good and consistent recoveries of the three compounds were obtained: 88-91% for mepivacaine, 87-89% for ropivacaine and 88-91% for bupivacaine. The limit of quantification for three compounds in human serum was 2 ng/ml for mepivacaine, 5 ng/ml for bupivacaine and ropivacaine. This method may be useful in clinical and forensic applications for the determination or identification of the local anesthetic drugs: bupivacaine, mepivacaine or ropivacaine.
已开发出一种高效液相色谱(HPLC)方法,用于同时分析属于哌啶并[1,2-a]嘧啶-6-酮类的局部麻醉酰胺类药物布比卡因、甲哌卡因和罗哌卡因。该方法使用填充有5微米颗粒的C(18)反相柱(内径150×4.6毫米),并连接紫外检测器。流动相由乙腈-甲醇-30 mM磷酸二氢钠(pH 5.6)(100:100:300,v/v/v)组成,流速为1毫升/分钟。在210纳米处监测洗脱液的吸光度。三种化合物的保留时间分别为:4.6分钟(甲哌卡因)、9.7分钟(罗哌卡因)和16.4分钟(布比卡因)。采用这种样品制备方法,三种化合物获得了良好且一致的回收率:甲哌卡因88 - 91%,罗哌卡因87 - 89%,布比卡因88 - 91%。人血清中三种化合物的定量限分别为:甲哌卡因2纳克/毫升,布比卡因和罗哌卡因为5纳克/毫升。该方法可能在临床和法医应用中用于测定或鉴定局部麻醉药物布比卡因、甲哌卡因或罗哌卡因。