The Pharmacokinetic Effect of Itraconazole and Voriconazole on Ripretinib in Beagle Dogs by UPLC-MS/MS Technique

• Published in: Drug design, development and therapy Vol. 15; pp. 4865 - 4873
• Main Authors: Wang, Hui-Jun, Zhou, Chun-Yan, Su, Yan-Ding, Gou, Kai-Feng, Geng, Xiao-Nan, Qiu, Xiang-Jun
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press Limited 01.01.2021; Taylor & Francis Ltd; Dove; Dove Medical Press
• Subjects: Acetic acid; Acetonitrile; Administration, Oral; Animal experimentation; Animals; Antifungal agents; beagle dog; Caustic soda; Chromatography, High Pressure Liquid; Design of experiments; Dogs; Drug dosages; Ethyl acetate; Experimental design; Female; Formic acid; Fungal infections; Ion pairs; Itraconazole; Itraconazole - blood; Itraconazole - chemistry; Itraconazole - pharmacokinetics; Laboratory animals; Male; Mass spectrometry; Metabolism; Methods; Mutation; Naphthyridines - blood; Naphthyridines - chemistry; Naphthyridines - pharmacokinetics; Oral administration; Organic compounds; Original Research; Pharmacokinetics; Pharmacology; Plasma; Plasma physics; ripretinib; Scientific imaging; Tandem Mass Spectrometry; Triazoles; uplc-ms/ms; Urea - analogs & derivatives; Urea - blood; Urea - chemistry; Urea - pharmacokinetics; Voriconazole; Voriconazole - blood; Voriconazole - chemistry; Voriconazole - pharmacokinetics; China; pharmacokinetics; UPLC-MS/MS; itraconazole; voriconazole; ripretinib; beagle dog
• ISSN: 1177-8881; 1177-8881
• DOI: 10.2147/DDDT.S337864

A new UPLC-MS/MS technique for the determination of ripretinib in beagle dog plasma was developed, and the pharmacokinetic effects of voriconazole and itraconazole on ripretinib in beagle dogs were studied. After extraction with ethyl acetate under alkaline conditions, ripretinib was detected using avapritinib as the internal standard (IS). The mobile phases were 0.1% formic acid-acetonitrile. The scanning method was multi-reaction monitoring using ESI+ source, and the ion pairs for ripretinib and IS were m/z 509.93→416.85 and 499.1→482.09, respectively. This animal experiment adopted a three period self-control experimental design. In the first period, ripretinib was orally administered to six beagle dogs at a dose of 5 mg/kg. In the second period, the same six beagle dogs were orally given itraconazole at a dose of 7 mg/kg, after 30 min, ripretinib was orally given. In the third period, voriconazole at a dose of 7 mg/kg was given orally, and then ripretinib was orally given. At different time points, the blood samples were collected. The concentration of ripretinib was detected, and the pharmacokinetic parameters of ripretinib were calculated. Ripretinib had a good linear relationship in the range of 1-1000 ng/mL. The precision, accuracy, recovery, matrix effect and stability met the requirements of the guiding principles. After erdafitinib combined with itraconazole, the C and AUC of ripretinib increased by 38.35% and 36.36%, respectively, and the t was prolonged to 7.53 h. After ripretinib combined with voriconazole, the C and AUC of ripretinib increased by 37.44% and 25.52%, respectively, and the t was prolonged to 7.33 h. A new and reliable UPLC-MS/MS technique was fully optimized and developed to detect the concentration of ripretinib in beagle dog plasma. Itraconazole and voriconazole could inhibit the metabolism of ripretinib in beagle dogs and increase the plasma exposure of ripretinib.