Department of Pharmaceutics, Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.
International Center for Bioavailability, Pharmaceutical, and Clinical Research, Obour City, Egypt.
Biomed Chromatogr. 2022 Sep;36(9):e5381. doi: 10.1002/bmc.5381. Epub 2022 Jul 13.
This research developed and validated a highly sensitive and selective UPLC-MS/MS approach using a triple quadrupole mass spectrometer for quantifying favipiravir. Moreover, we introduced a study evaluating bioequivalence using two drugs, Favibrivix and Avigan, containing favipiravir. Lean Six Sigma verified the capacity and performance of the process. Protein precipitation extraction was utilized to extract favipiravir from the collected human matrices. We used an Acquity UPLCr BEH HILIC column and valproic acid as an internal standard. Furthermore, we conducted the procedure using an isocratic elution comprising acetonitrile and 0.005% ammonia in water (75:25, v/v), a flow rate of 0.25 ml/min, a temperature controlled at 10°C and an injection volume of 1.0 μl. Our UPLC-MS/MS process has a broad range (50-10,000 ng/ml) with a determination coefficient of 0.9980. We validated the method in line with the US Food and Drug Administration. The findings revealed that the test, Favibrivix 200 mg/tablet, and the reference, Avigan® 200 mg/tablet, were statistically bioequivalent in healthy Egyptian participants.
本研究开发并验证了一种使用三重四极杆质谱仪的超高效液相色谱-串联质谱法,用于定量检测法匹拉韦。此外,我们还开展了一项使用两种含有法匹拉韦的药物(Favibrivix 和 Avigan)评估生物等效性的研究。精益六西格玛验证了该过程的能力和性能。采用蛋白沉淀萃取法从收集的人体基质中提取法匹拉韦。我们使用 Acquity UPLC BEH HILIC 柱和缬草酸作为内标。此外,我们采用等度洗脱,包含乙腈和水中的 0.005%氨(75:25,v/v),流速为 0.25ml/min,温度控制在 10°C,进样体积为 1.0μl。我们的 UPLC-MS/MS 方法具有较宽的检测范围(50-10000ng/ml),决定系数为 0.9980。该方法符合美国食品和药物管理局的要求。研究结果表明,在健康的埃及参与者中,受试制剂 Favibrivix 200mg/片和参比制剂 Avigan®200mg/片具有统计学意义上的生物等效性。