Zhang Fengyichi, Guo Fanxi, Zhao Xinyu, Li Chongyang, Wang Junli, Wang Mengyun, Ma Ruixia, Chen Baochang, Miao Qiangqiang, Wang Yimeng, Wang Zihan, Cao Di, Yu Zugong
Laboratory of Veterinary Pharmacology and Toxicology, Department of Basic Veterinary Medicine, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China.
Front Pharmacol. 2025 Feb 13;16:1544215. doi: 10.3389/fphar.2025.1544215. eCollection 2025.
A rapid, sensitive and reliable ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was developed and validated for the simultaneous quantitation of pyrantel (PYR), praziquantel (PRA), febantel (FBT) and its active metabolites, fenbendazole (FEN) and oxfendazole (OXF) in dog plasma. Fenbendazole-D3 (FEN-D3) was used as an internal standard (IS). The analytes and IS were prepared using simple protein precipitation (PP) combined with liquid-liquid extraction (LLE). Chromatographic analysis was performed on UPLC BEH C column using acetonitrile-0.1% formic acid in water for gradient elution. Detection was carried out in multiple reaction monitoring (MRM) mode under positive electrospray ionization. The standard curves were linear through the concentration range of 4-240 ng/mL for PYR and OXF, 15-900 ng/mL for PRA, 2-120 ng/mL for FBT and 10-600 ng/mL for FEN with all correlation coefficients >0.99. The intra-and inter-batch precision was 1.08%-14.26% and accuracy was from 90.66% to 110.28%. The mean extraction recoveries for the analytes and IS were >90%. The total run time was 9.0 min. The developed method was successfully applied to a bioequivalence study after oral administration of compound febantel tablets in 38 healthy dogs.
建立了一种快速、灵敏且可靠的超高效液相色谱-串联质谱法(UPLC-MS/MS),用于同时定量犬血浆中的噻嘧啶(PYR)、吡喹酮(PRA)、非班太尔(FBT)及其活性代谢物芬苯达唑(FEN)和奥芬达唑(OXF)。芬苯达唑-D3(FEN-D3)用作内标(IS)。采用简单的蛋白沉淀(PP)结合液液萃取(LLE)制备分析物和内标。在UPLC BEH C柱上进行色谱分析,以乙腈-0.1%甲酸水溶液进行梯度洗脱。在正电喷雾电离下的多反应监测(MRM)模式下进行检测。吡喹酮和奥芬达唑在4-240 ng/mL浓度范围内、吡喹酮在15-900 ng/mL浓度范围内、非班太尔在2-120 ng/mL浓度范围内、芬苯达唑在10-600 ng/mL浓度范围内,标准曲线呈线性,所有相关系数均>0.99。批内和批间精密度为1.08%-14.26%,准确度为90.66%-110.28%。分析物和内标的平均萃取回收率>90%。总运行时间为9.0分钟。所建立的方法成功应用于38只健康犬口服复方非班太尔片后的生物等效性研究。