[1] Sekine T, Miyazaki H, Endou H.Molecular physiology of renal organic anion transporters[J].Am J Physiol Renal Physiol, 2006, 290(2):F251-F261. [2] Choudhuri S, Klaassen CD.Structure, function, expression, genomic organization, and single nucleotide polymorphisms of human ABCB1 (MDR1), ABCC (MRP), and ABCG2 (BCRP)efflux transporters[J].Int J Toxicol,2006, 25(4):231-259. [3] Sweet DH.Organic anion transporter (Slc22a)family members as mediators of toxicity[J].Toxicol Appl Pharmacol, 2005, 204(3):198-215. [4] Shitara Y, Horiea T, Sugiyama Y.Transporters as a determinant of drug clearance and tissue distribution[J].Eur J Pharm Sci, 2006, 27(5):425-446. [5] Funk C, Ponelle C, Scheuermann G, et a1.Cholestatic potential of troglitazone as a possible factor contributing to troglitazone-induced hepatotoxicity:in vivo and in vitro interaction at the canalicular bile salt export pump (Bsep)in the rat[J].Mol Pharmacol, 2001, 59(3):627-635. [6] Wang DS, Kusuhara H, Kato Y, et al.Involvement of organic cation transporter 1 in the lactic acidosis caused by metformin[J].Mol Pharmacol, 2003, 63(4):844-848. [7] Vavricka SR, Van Montfoort J, Ha HR, et a1.Interactions of rifamycin SV and rifampicin with organic anion uptake systems of human liver[J].Hepatology, 2002, 36 (1):164-172. [8] Kajinami K, Takekoshi N, Saito Y.Pitavastatin:efficacy and safety profiles of a novel synthetic HMG-CoA reductase inhibitor[J].Cardiovasc Drug Rev, 2003, 21(3):199-215. [9] Dominguez MF, Macias RI, Izco-Basurko I, et al.Low in vivo toxicity of a novel cisplatin-ursodeoxy cholic derivative (Bamet-UD2).with enhanced cytostatic activity versus liver tumors[J].J Pharmacol Exp Ther, 2001, 297 (3):1106-1112. [10] Nakanishi T, Tamai I, Takaki A, et al.Cancer cell-targeted drug delivery utilizing oligopeptide transport activity [J].Int J Cancer, 2000, 88(2):274-280. [11] Yamada I, Fukunari A, Osajima T, et al.Pharmacokinetics pharmacodynamics of Y-700, a novel xanthine oxidase inhibitor, in rats and man[J].Nucleosides Nucleotides Nucleic Acids, 2004, 23(8 9):1123-1125. [12] Sai Y, Kato Y, Nakamura K, et al.Carrier-mediated hepatic uptake of a novel nonrenal excretion type uric acid generation inhibitor, Y-700[J].J Pharm Sci, 2006, 95 (2):336-347. [13] Marchetti S, Mazzanti R, Beijnen JH, et al.Concise review:Clinical relevance of drug drug and herb drug interactions mediated by the ABC transporter ABCB1 (MDR1, P-gly coprotein)[J].Oncologist, 2007, 12(8):927-941. [14] Shitara Y, Hirano M, Sato H, et a1.Gemfibrozil and its glucuronide inhibit the organic anion transporting polypeptide 2 (OATP2 OATP1B1:SLC21A6)-mediated hepatic uptake and CYP2C8-mediated metabolism of cerivastatin: analy sis of the mechanism of the clinically relevant drugdrug interaction between cerivastatin and gemfibrozil[J].J Pharmacol Exp Ther, 2004, 311(1):228-236. [15] Farkas D, Greenblatt DJ.Influence of fruit juices on drug disposition:discrepancies between in vitro and clinical studies[J].Expert Opin Drug Metab Toxicol, 2008, 4 (4):381-393. [16] 范岚, 谢海棠, 周宏灏.中西药合用治疗肿瘤的相互作用及其机制探讨[J].中国临床药理学与治疗学,2007, 12(2):134-139. [17] 毛晓琴, 谢海棠, 周宏灏.多药耐药蛋白和CYP3A4介导的中草药-西药相互作用[J].中国临床药理学与治疗学, 2007, 12(7):728-734. [18] Yang XX, Hu ZP, Duan W, et a1.Drug-herb interactions: eliminating toxicity with hard drug design[J].Curr Pharm Des, 2006, 12(35):4649-4664. [19] Huang SM, Strong JM, Zhang L, et al.New era in drug interaction evaluation:US Food and Drug Administration update on CYP enzymes, transporters, and the guidance process[J].J Clin Pharmacol, 2008, 48(6):662-670. [20] Huang SM, Temple R, Throckmorton DC, et al.Drug interaction studies:study design, data analysis, and implications for dosing and labeling[J].Clin Pharmacol Ther, 2007, 81(2):298-304. [21] Hammerle SP, Rothen RB, Kramer SD, et al.P-Gly coprotein in cell cultures:a combined approach to study expression, localisation, and functionality in the confocal microscope[J].Eur J Pharm Sci, 2000, 12(1):69-77. [22] 周昕.药物吸收体外研究方法的概述[J].中国临床药理学与治疗学, 2006, 11(4):379-384. [23] Chang C, Swaan PW.Computational approaches to modeling drug transporters[J].Eur J Pharm Sci, 2006, 27(5): 411-424. [24] 马秉亮, 吴玉林, 刘国卿.P-gp 及对抗P-gp 介导多药耐药的研究现状[J].中国临床药理学与治疗学,2006, 11(1):14-21. [25] DemelMA, Schwaha R, Kr?mer O, et a1.In silico prediction of substrate properties for ABC-multidrug transporters[J].Expert Opin Drug Metab Toxicol, 2008, 4(9):1167-1180. |