[1]Evers R, Chu XY. Role of the murine organic anion-transporting polypeptide 1b2 (Oatp1b2) in drug disposition and hepatotoxicity[J]. Mol Pharmacol, 2008, 74 (2): 309-311.
[2]Tsuji A. Impact of transporter-mediated drug absorption, distribution, elimination and drug interactions in antimicrobial chemotherapy[J]. J Infect Chemother, 2006, 12 (5):241-250.
[3]Shitara Y, Horie T, Sugiyama Y. Transporters as a determinant of drug clearance and tissue distribution[J]. Eur J Pharm Sci, 2006, 27(5): 425-446.
[4]刘克辛. 转运体介导的药物相互作用与临床安全用药[J]. 大连医科大学学报, 2012, 34(1): 1-8.
[5]刘琦, 刘克辛. 代谢酶和转运体介导的中药-西药相互作用的药动学机制研究进展[J]. 药学学报, 2015, 50(4): 406-412.
[6]Liu Q, Wang C, Meng Q, et al. MDR1 and OAT1/OAT3 mediate the drug-drug interaction between puerarin and methotrexate[J]. Pharm Res, 2014, 31: 1120-1132.
[7]Jiang R, Dong J, Li X, et al. Molecular mechanisms governing differential pharmacokinetics of ginsenosides and potential for ginsenoside-perpetrated herb-drug interactions on OATP1B3[J]. Br J Pharmacol, 2015, 172: 1059-1073.
[8]Rodrigues AC. Efflux and uptake transporters as determinants of statin response[J]. Expert Opin Drug Metab Toxicol, 2010, 6(5): 621-632.
[9]Giacomini KM, Huang SM, Tweedie DJ, et al. Membrane transporters in drug development[J]. Nat Rev Drug Discov, 2010, 9(3): 215-236.
[10]陈涛. 基于LC-MS/MS绝对定量人肝细胞中药物转运体及其应用[D]. 广东:广东药科大学, 2016: 1-84.
[11]Zhang L, Reynolds KS, Zhao P, et al. Drug interactions evaluation: An integrated part of risk assessment of therapeutics[J]. Toxicol Appl Pharmacol, 2010, 243(2): 134-145.
[12]Bi YA, Kimoto E, Sevidal S, et al. In vitro evaluation of hepatic transporter-mediated clinical drug-drug interactions: hepatocyte model optimization and retrospective investigation[J]. Drug Metab Dispos, 2012, 40(6): 1085-1092.
[13]Hartman JC, Brouwer K, Melvin L, et al. Evaluation of the endothelin receptor antagonists ambrisentan, darusentan, bosentan, and sitaxsentan as substrates and inhibitors of hepatobiliary transporters in sandwich-cultured human hepatocytes[J]. Can J Physiol Pharmacol, 2010, 88: 682-691.
[14]FDA: Guidance for Industry: Drug interaction studies-study design, data analysis, implications for dosing, and labeling recommendations[EB/OL]. 2012. http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm
[15]韩永龙, 孟祥乐, 李丹, 等. 清开灵注射剂等5种中药注射剂对大鼠肝微粒体CYP3A的体外抑制作用[J]. 中国中药杂志, 2011, 36(4): 492-495. |