1,687
Views
0
CrossRef citations to date
0
Altmetric
Research Article

Assessments of CYP‑inhibition‑based drug–drug interaction between vonoprazan and poziotinib in vitro and in vivo

, , , , , , , , & show all
Pages 356-361 | Received 21 Jun 2022, Accepted 20 Jan 2023, Published online: 02 Feb 2023

References

  • Benet LZ, Bowman CM, Koleske ML, Rinaldi CL, Sodhi JK. 2019. Understanding drug-drug interaction and pharmacogenomic changes in pharmacokinetics for metabolized drugs. J Pharmacokinet Pharmacodyn. 46(2):155–163.
  • Dungo RT, Keating GM. 2013. Afatinib: first global approval. Drugs. 73(13):1503–1515.
  • Echizen H. 2016. The first-in-class potassium-competitive acid blocker, vonoprazan fumarate: pharmacokinetic and pharmacodynamic considerations. Clin Pharmacokinet. 55(4):409–418.
  • El Rouby N, Lima JJ, Johnson JA. 2018. Proton pump inhibitors: from CYP2C19 pharmacogenetics to precision medicine. Expert Opin Drug Metab Toxicol. 14(4):447–460.
  • Eriksson LC. 1978. Preparation of liver microsomes with high recovery of endoplasmic reticulum and a low grade of contamination. Biochim Biophys Acta. 508(1):155–164.
  • Gandhi S, Fleet JL, Bailey DG, McArthur E, Wald R, Rehman F, Garg AX. 2013. Calcium-channel blocker-clarithromycin drug interactions and acute kidney injury. JAMA. 310(23):2544–2553.
  • Garnock-Jones KP. 2015. Vonoprazan: first global approval. Drugs. 75(4):439–443.
  • Hiraide M, Minowa Y, Nakano Y, Suzuki K, Shiga T, Nishio M, Miyoshi J, Takahashi H, Hama T. 2019. Drug interactions between tyrosine kinase inhibitors (gefitinib and erlotinib) and warfarin: assessment of international normalized ratio elevation characteristics and in vitro CYP2C9 activity. J Oncol Pharm Pract. 25(7):1599–1607.
  • Hu LM, Dai DP, Hu GX, Yang JF, Xu RA, Yang LP, Qian JC, Ge RS, Cai JP. 2012. Genetic polymorphisms and novel allelic variants of CYP2C19 in the Chinese Han population. Pharmacogenomics. 13(14):1571–1581.
  • Ji W, Shen J, Wang B, Chen F, Meng D, Wang S, Dai D, Zhou Y, Wang C, Zhou Q. 2021. Effects of dacomitinib on the pharmacokinetics of poziotinib in vivo and in vitro. Pharm Biol. 59(1):457–464.
  • Kato H. 2020. Computational prediction of cytochrome P450 inhibition and induction. Drug Metab Pharmacokinet. 35(1):30–44.
  • Kim E, Kim H, Suh K, Kwon S, Lee G, Park NH, Hong J. 2013. Metabolite identification of a new tyrosine kinase inhibitor, HM781-36B, and a pharmacokinetic study by liquid chromatography/tandem mass spectrometry. Rapid Commun Mass Spectrom. 27(11):1183–1195.
  • Kim JY, Park K, Im SA, Jung KH, Sohn J, Lee KS, Kim JH, Yang Y, Park YH. 2020. Clinical implications of HER2 mRNA expression and intrinsic subtype in refractory HER2-positive metastatic breast cancer treated with pan-HER inhibitor, poziotinib. Breast Cancer Res Treat. 184(3):743–753.
  • Kim TY, Han HS, Lee KW, Zang DY, Rha SY, Park YI, Kim JS, Lee KH, Park SH, Song EK, et al. 2019. A phase I/II study of poziotinib combined with paclitaxel and trastuzumab in patients with HER2-positive advanced gastric cancer. Gastric Cancer. 22(6):1206–1214.
  • Kogame A, Takeuchi T, Nonaka M, Yamasaki H, Kawaguchi N, Bernards A, Tagawa Y, Morohashi A, Kondo T, Moriwaki T, et al. 2017. Disposition and metabolism of TAK-438 (vonoprazan fumarate), a novel potassium-competitive acid blocker, in rats and dogs. Xenobiotica. 47(3):255–266.
  • Lee B, Ji HK, Lee T, Liu KH. 2015. Simultaneous screening of activities of five cytochrome P450 and four uridine 5′-diphospho-glucuronosyltransferase enzymes in human liver microsomes using cocktail incubation and liquid chromatography-tandem mass spectrometry. Drug Metab Dispos. 43(7):1137–1146.
  • Liu L, Sun S, Rui H, Li X. 2017. In vitro inhibitory effects of dihydromyricetin on human liver cytochrome P450 enzymes. Pharm Biol. 55(1):1868–1874.
  • Ma J, Wang S, Zhang M, Zhang Q, Zhou Y, Lin C, Lin G, Wang X. 2015. Simultaneous determination of bupropion, metroprolol, midazolam, phenacetin, omeprazole and tolbutamide in rat plasma by UPLC-MS/MS and its application to cytochrome P450 activity study in rats. Biomed Chromatogr. 29(8):1203–1212.
  • Marabotto E, Ziola S, Savarino V, Giannini EG, Furnari M, Bodini G, Zingone F, Ghisa M, Barberio B, Zentilin P, et al. 2020. Vonoprazan fumarate for the treatment of gastric ulcers: a short review on emerging data. Clin Exp Gastroenterol. 13:99–104.
  • Martinucci I, Blandizzi C, Bodini G, Marabotto E, Savarino V, Marchi S, de Bortoli N, Savarino E. 2017. Vonoprazan fumarate for the management of acid-related diseases. Expert Opin Pharmacother. 18(11):1145–1152.
  • Mori H, Suzuki H. 2019. Role of acid suppression in acid-related diseases: proton pump inhibitor and potassium-competitive acid blocker. J Neurogastroenterol Motil. 25(1):6–14.
  • Murakami K, Sakurai Y, Shiino M, Funao N, Nishimura A, Asaka M. 2016. Vonoprazan, a novel potassium-competitive acid blocker, as a component of first-line and second-line triple therapy for Helicobacter pylori eradication: a phase III, randomised, double-blind study. Gut. 65(9):1439–1446.
  • Nishihara M, Yamasaki H, Czerniak R, Jenkins H. 2019. In vitro assessment of potential for CYP-inhibition-based drug-drug interaction between vonoprazan and clopidogrel. Eur J Drug Metab Pharmacokinet. 44(2):217–227.
  • Oshima T, Miwa H. 2018. Potent potassium-competitive acid blockers: a new era for the treatment of acid-related diseases. J Neurogastroenterol Motil. 24(3):334–344.
  • Prommer E. 2004. Gefitinib: a new agent in palliative care. Am J Hosp Palliat Care. 21(3):222–227.
  • Prout W. 1974. On the nature of the acid and saline matters usually existing in the stomachs of animals. Gut. 15(1):45.1–49.1.
  • Rosell R, Cardona Zorrilla AF. 2021. Poziotinib treatment in intractable NSCLC: epidermal growth factor receptor and human epidermal growth factor receptor 2 exon 20 insertion mutation disease. Eur J Cancer. 149:233–234.
  • Sachs G, Shin JM, Munson K, Scott DR. 2014. Gastric acid-dependent diseases: a twentieth-century revolution. Dig Dis Sci. 59(7):1358–1369.
  • Sevrioukova IF, Poulos TL. 2015. Current approaches for investigating and predicting cytochrome P450 3A4-ligand interactions. Adv Exp Med Biol. 851:83–105.
  • Shen J, Wang B, Wang S, Chen F, Meng D, Jiang H, Zhou Y, Geng P, Zhou Q, Liu B. 2020. Effects of voriconazole on the pharmacokinetics of vonoprazan in rats. Drug Des Dev Ther. 14:2199–2206.
  • Shin JM, Inatomi N, Munson K, Strugatsky D, Tokhtaeva E, Vagin O, Sachs G. 2011. Characterization of a novel potassium-competitive acid blocker of the gastric H,K-ATPase, 1-[5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamin e monofumarate (TAK-438. J Pharmacol Exp Ther. 339(2):412–420.
  • Shin JM, Kim N. 2013. Pharmacokinetics and pharmacodynamics of the proton pump inhibitors. J Neurogastroenterol Motil. 19(1):25–35.
  • Shirley M. 2018. Dacomitinib: first global approval. Drugs. 78(18):1947–1953.
  • Sugano K. 2018. Vonoprazan fumarate, a novel potassium-competitive acid blocker, in the management of gastroesophageal reflux disease: safety and clinical evidence to date. Therap Adv Gastroenterol. 11:1756283x17745776.
  • Sugimoto M, Hira D, Murata M, Kawai T, Terada T. 2020. Effect of antibiotic susceptibility and CYP3A4/5 and CYP2C19 genotype on the outcome of vonoprazan-containing Helicobacter pylori eradication therapy. Antibiotics. 9(10):645.
  • Suzuki A, Iida I, Hirota M, Akimoto M, Higuchi S, Suwa T, Tani M, Ishizaki T, Chiba K. 2003. CYP isoforms involved in the metabolism of clarithromycin in vitro: comparison between the identification from disappearance rate and that from formation rate of metabolites. Drug Metab Pharmacokinet. 18(2):104–113.
  • Suzuki Y, Yoshihashi T, Takahashi K, Furuya K, Ohkohchi N, Oda T, Homma M. 2021. Drug-drug interaction between tacrolimus and vonoprazan in kidney transplant recipients. JCM. 10(17):3964.
  • Tyzack JD, Kirchmair J. 2019. Computational methods and tools to predict cytochrome P450 metabolism for drug discovery. Chem Biol Drug Des. 93(4):377–386.
  • Wang J, Chen F, Jiang H, Xu J, Meng D, Geng P, Dai D, Hu J, Zhou Y, Zhou Q, et al. 2020. Inhibition and induction by poziotinib of different rat cytochrome P450 enzymes in vivo and in an in vitro cocktail method. Front Pharmacol. 11:593518.
  • Wang Y, Jin Y, Yun X, Wang M, Dai Y, Xia Y. 2018. Co-administration with simvastatin or lovastatin alters the pharmacokinetic profile of sinomenine in rats through cytochrome P450-mediated pathways. Life Sci. 209:228–235.
  • Wang Y, Wang C, Wang S, Zhou Q, Dai D, Shi J, Xu X, Luo Q. 2020. Cytochrome P450-based drug-drug interactions of vonoprazan in vitro and in vivo. Front Pharmacol. 11:53.
  • Werk AN, Cascorbi I. 2014. Functional gene variants of CYP3A4. Clin Pharmacol Ther. 96(3):340–348.
  • Yamasaki H, Kawaguchi N, Nonaka M, Takahashi J, Morohashi A, Hirabayashi H, Moriwaki T, Asahi S. 2017. In vitro metabolism of TAK-438, vonoprazan fumarate, a novel potassium-competitive acid blocker. Xenobiotica. 47(12):1027–1034.
  • Yoneyama T, Teshima K, Jinno F, Kondo T, Asahi S. 2016. A validated simultaneous quantification method for vonoprazan (TAK-438F) and its 4 metabolites in human plasma by the liquid chromatography-tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 1015–1016:42–49.