Polettini A, Huestis M A
Chemistry and Drug Metabolism Section, IRP, NIDA, NIH, Baltimore, MD 21224, USA.
J Chromatogr B Biomed Sci Appl. 2001 Apr 25;754(2):447-59. doi: 10.1016/s0378-4347(01)00029-9.
For the first time, an LC-MS-MS method has been developed for the simultaneous analysis of buprenorphine (BUP), norbuprenorphine (NBUP), and buprenorphine-glucuronide (BUPG) in plasma. Analytes were isolated from plasma by C18 SPE and separated by gradient RP-LC. Electrospray ionization and MS-MS analyses were carried out using a PE-Sciex API-3000 tandem mass spectrometer. The m/z 644-->m/z 468 transition was monitored for BUPG, whereas for BUP, BUP-d4, NBUP, and NBUP-d3 it was necessary to monitor the surviving parent ions in order to achieve the required sensitivity. The method exhibited good linearity from 0.1 to 50 ng/ml (r2> or =0.998). Extraction recovery was higher than 77% for BUPG and higher than 88% for both BUP and NBUP. The LOQ was established at 0.1 ng/ml for the three analytes. The method was validated on plasma samples collected in a controlled intravenous and sublingual buprenorphine administration study. Norbuprenorphine-glucuronide was also tentatively detected in plasma by monitoring the m/z 590-->m/z 414 transition.
首次开发了一种液相色谱-串联质谱法,用于同时分析血浆中的丁丙诺啡(BUP)、去甲丁丙诺啡(NBUP)和丁丙诺啡葡萄糖醛酸苷(BUPG)。通过C18固相萃取从血浆中分离分析物,并采用梯度反相液相色谱进行分离。使用PE-Sciex API-3000串联质谱仪进行电喷雾电离和串联质谱分析。对BUPG监测m/z 644→m/z 468的跃迁,而对于BUP、BUP-d4、NBUP和NBUP-d3,为达到所需灵敏度,有必要监测母离子。该方法在0.1至50 ng/ml范围内呈现良好的线性(r2≥0.998)。BUPG的萃取回收率高于77%,BUP和NBUP的萃取回收率均高于88%。三种分析物的定量下限均设定为0.1 ng/ml。该方法在一项丁丙诺啡静脉注射和舌下给药对照研究中采集的血浆样本上得到验证。通过监测m/z 590→m/z 414的跃迁,还在血浆中初步检测到了去甲丁丙诺啡葡萄糖醛酸苷。