Liu Cuiru, Li Yingchao, Yang Rujie, Zhang Shuqi, Zhao Longshan, Zhang Tianhong
Shenyang Pharmaceutical University, School of Pharmacy, Shenyang, People's Republic of China.
Biomed Chromatogr. 2018 Oct;32(10):e4300. doi: 10.1002/bmc.4300. Epub 2018 Jul 16.
A prodrug of tapentadol, namely tapentadol carbamate (WWJ01), was synthesized to improve the bioavailability of tapentadol owing to its extensive first-pass metabolism. In this study, a highly rapid and sensitive UPLC-MS/MS method was developed and validated for the simultaneous determination of tapentadol and WWJ01 in rat plasma with fluconazole as an internal standard. The analytes and internal standard were treated by methanol and then separated on a Phenomenex Kinetex® XB-C (2.1 × 50 mm × 2.6 μm) column at a flow rate of 0.3 mL/min. The mobile phase comprised methanol and water with a gradient elution. The mass transition ion-pairs were m/z 222.2 → 107.0, m/z 293.2 → 71.9 and m/z 307.1 → 220.0 for tapentadol, WWJ01 and IS, respectively. Excellent linearity was observed over the concentration range of 2-1250 ng/mL (r = 0.995) with a lower limit of quantification of 2 ng/mL for both tapentadol and WWJ01. The intra- and inter-day accuracy and precision for all quality control samples were within ±15%. The validated method was accurate, rapid and reproducible, and was successfully applied to a pharmacokinetic study of tapentadol and WWJ01.
由于曲马多存在广泛的首过代谢,为提高其生物利用度,合成了曲马多的前体药物,即曲马多氨基甲酸酯(WWJ01)。在本研究中,建立了一种高效快速且灵敏的超高效液相色谱-串联质谱(UPLC-MS/MS)方法,并以氟康唑作为内标物,用于同时测定大鼠血浆中的曲马多和WWJ01。分析物和内标物用甲醇处理后,在Phenomenex Kinetex® XB-C(2.1×50 mm×2.6μm)色谱柱上以0.3 mL/min的流速进行分离。流动相由甲醇和水组成,采用梯度洗脱。曲马多、WWJ01和内标的质量转移离子对分别为m/z 222.2→107.0、m/z 293.2→71.9和m/z 307.1→220.0。在2 - 1250 ng/mL的浓度范围内观察到了良好的线性关系(r = 0.995),曲马多和WWJ01的定量下限均为2 ng/mL。所有质量控制样品的日内和日间准确度及精密度均在±15%以内。所验证的方法准确、快速且可重复,并成功应用于曲马多和WWJ01的药代动力学研究。