[1] 操锋, 平其能, 陈军. 口服前药研究:机遇与挑战[J]. 药学学报, 2008, 43(4): 343-349. [2] Stella VJ, Himmelstein KJ.Prodrugs and site-specific drug delivery[J]. J Med Chem, 1980, 23(12): 1275-1282. [3] Testa B.Prodrugs: bridging pharmacodynamic/pharmacokinetic gaps[J]. Curr Opin Chem Biol, 2009, 13(3): 338-344. [4] Ettmayer P, Amidon GL, Clement B, et al.Lessons learned from marketed and investigational prodrugs[J]. J Med Chem, 2004, 47(10): 2393-2404. [5] Beaumont K, Webster R, Gardner I, et al.Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: challenges to the discovery scientists[J]. Curr Drug Metab, 2003, 4(6): 461-485. [6] 段艳冰, 黄德虎, 刘实, 等. 磷酸酯化在新药开发中的应用[J].医药导报,2011, 30(8): 1056-1057. [7] 何亮. 前药的研究进展[J]. 世界临床药物, 2006, 27(1): 55-58. [8] 李铭东, 吉民. 肿瘤活化前药的研究与应用进展[J]. 药品评价, 2006, 3(3): 206-213. [9] 易静. 肿瘤的酶-前药疗法[J]. 国外医学肿瘤学分册, 2005, 32(6): 413-416. [10] Wu KM.A new classification of prodrugs: regulatory perspectives[J]. Pharmaceuticals, 2009, 2(3): 77-81. [11] 刘昌孝, 主编. 实用药物动力学[M]. 1版.北京: 中国医药科技出版社, 2003:241-254. [12] Rautio J, Kumpulainen H, Heimbach T, et al.Prodrugs: design and clinical applications[J]. Nat Rev Drug Discov, 2008, 7(3): 255-270. [13] Testa B.Prodrug research: futile or fertile[J]. Biochem Pharmacol, 2004, 68(11): 2097-2106. [14] Cundy KC, Sastry S, Luo W, et al.Clinical pharmacokinetics of XP13512, a novel transported prodrug of Gabapentin[J]. J Clin Pharmacol, 2008, 48(12): 1378-1388. [15] Cundy KC, Branch R, Chernov-Rogan T, et al.XP13512[(±)-1-([(α-lsobutanoyloxyethoxy)carbonyl] aminometgyl)-1-cyclohexane Acetic Acid], a novel Gabapentin prodrug: Ⅰ. Design, Synthesis, Enzymatic conversion to Gabapentin, and transport by intestinal solute transporters[J]. J Pharmacol Exp Ther, 2004, 311(1): 315-323. [16] Cundy KC, Annamalai T, Bu L, et al.XP13512[(±)-1-([(α-lsobutanoyloxyethoxy) carbonyl]aminometgyl) -1-cyclohexane Acetic Acid], a novel Gabapentin prodrug: Ⅱ. Improved oral bioavailability, dose proportionality, and colonic absorption compared with Gabapentin in rats and monkeys[J]. J Pharmacol Exp Ther, 2004, 311(1): 324-333. [17] Marathe PH, Kamath AV, Zhang Y, et al.Preclinical pharmacokinetics and in vitro metabolism of brivanib(BMS-540215), a potent VEGFR2 inhibitor and its alanine ester prodrug brivanib alaninate[J]. Cancer Chemother Pharmacol, 2009, 65(1): 55-66. [18] Gong J, Gan J, Caceres-Cortes J, et al.Metabolism and disposition of [14C]Brivanib Alaninate after oral administration to rats, monkeys and humans[J]. Drug Metab Dispo, 2011, 39(5): 891-903. [19] Mekhail T, Masson E, Fischer BS, et al.Metabolism, excretion and pharmacokinetics of oral Brivanib in patients with advanced or metastatic solid tumors[J]. Drug Metab Dispo, 2010, 38(11): 1962-1966. [20] Jonker DJ, Rosen LS, Sawyer MB, et al.A phase Ⅰstudy to determine the safety, pharmacokinetics and pharmacodynamics of a dual VEGFR and FGFR inhibitor, brivanib, in patients with advanced or metastatic solid tumors[J]. Ann Oncol, 2011, 22(6): 1413-1419. [21] Park JW, Finn RS, Kim JS, et al.Phase Ⅱ, open-label study of Brivanib as first-line therapy in patients with advanced hepatocellular carcinoma[J]. Clin Cancer Res, 2011, 17(7): 1973-1983. [22] Chapman TM, Ploker GL, Perry CM.Fosamprenavir: a review of its use in the management of antiretroviral therapy-naive patients with HIV infection[J]. Drugs, 2004, 64(18): 2101-2124. [23] Wire MB, Shelton MJ, Studenberg S.Clinical pharmacokinetics and drug interactions of the Amprenavir prodrug[J]. Clin Pharmacokinet, 2006, 45(2): 137-168. [24] Furfine ES, Baker CT, Hale MR, et al.Preclinical pharmacology and pharmacokinetics of GW433908, a water-soluble prodrug of the human immunodeficiency virus protease inhibitor Amprenavir[J]. Antimicrob Agents Chemother, 2004, 48(3): 791-798. [25] Falcoz C, Jenkins JM, Bye C, et al.Pharmacokinetics of GW433908, a prodrug of Amprenavir, in healthy male volunteers[J]. J Clin Pharmacol, 2002, 42(8): 887-898. [26] Browne TR, Kugler AR, Eldon MA.Pharmacology and pharmacokinetics of fosphenytoin[J]. Neurology, 1996, 46(6): S3-S7. [27] Mahajan A, Singh K, Tandon VR, et al.Diacerein: a new symptomatic slow acting drug for osteoarthritis[J]. Drug Reviews, 2006, 8(3): 173-175. [28] Barditch-Crovo P, Toole J, Hendrix CW, et al.Anti-human immunodeficiency virus (HIV) activity, safety, and pharmacokinetics of Adefovir Dipivoxil (9-[2-(bis-pivaloyloxymethyl) -phosphonylmethoxyethyl]adenine) in HIV-infected patients[J]. J Infect Dis, 1997, 176(2): 406-413. [29] Qaqish RB, Mattes KA, Ritchie DJ.Adefovir Dipivoxil: a new antiviral agent for the treatment of Hepatitis B virus infection[J]. Clin Ther, 2003, 25(12): 3084-3099. [30] Sobue S, Sekiguchi K, Shimatani K, et al.Pharmacokinetics and safety of fosfluconazole after single intravenous bolus injection in healthy male Japanese volunteers[J]. J Clin Pharmacol, 2004, 44(3): 284-292. [31] He G, Massarella J, Ward P.Clinical pharmacokinetics of the prodrug Oseltamivir and its active metabolite Ro 64-0802[J]. Clin Pharmacokinet, 1999, 37(6): 471-484. [32] Pierra C, Amador A, Benzaria S, et al.Synthesis and pharmacokinetics of Valopicitabine (NM283), an efficient prodrug of the potent anti-HCV agent 2'-C-Methylcytidine[J]. J Med Chem, 2006, 49(22): 6614-6620. [33] Ishizuka H, Yoshiba S, Okabe H, et al.Clinical pharmacokinetics of Laninamivir, a novel long-acting neuraminidase inhibitor, after single and multiple inhaled doses of its prodrug, CS-8958, in healthy male volunteers[J]. J Clin Pharmacol, 2010, 50(11): 1319-1329. [34] Koyama K, Takahashi M, Nakai N, et al.Pharmacokinetics and disposition of CS-8958, a long-acting prodrug of the novel neuraminidase inhibitor laninamivir in rats[J]. Xenobiotica, 2010, 40(3): 207-216. [35] Hagihara K, Kazui M, Ikenaga H, et al.Comparison of formation of thiolactones and active metabolites of prasugrel and clopidogrel in rats and dogs[J]. Xenobiotica, 2009, 39(3): 218-226. [36] Farid NA, Smith RL, Gillespie TA, et al.The disposition of Prasugrel, a novel thienopyridine, in humans[J]. Drug Metab Dispo, 2007, 35(7): 1096-1104. [37] Smith RL, Gillespie TA, Rash TJ, et al.Disposition and metabolic fate of prasugrel in mice, rats, and dogs[J]. Xenobitica, 2007, 37(8): 884-901. [38] Gustafsson D, Elg M.The pharmacodynamics and pharmacokinetics of the oral direct thrombin inhibitor ximelagatran and its active metabolite melagatran: a mini-review[J]. Thromb Res, 2003, 109(Suppl 1): S9-15. [39] Eriksson UG, Bredberg U, Gislen K, et al.Pharmacokinetics and pharmacodynamics of ximelagatran, a novel oral direct thrombin inhibitor, in young healthy male subjects[J]. Eur J Clin Pharmacol, 2003, 59(1): 35-43. [40] Beumer JH, Eisesman JL, Gilbert JA, et al.Plasma pharmacokinetics and oral bioavailability of the 3,4,5,6-tetrahydrouridine(THU) prodrug, triacetyl-THU(taTHU), in mice[J]. Cancer Chemother Pharmacol, 2011, 67(2): 421-430. [41] 周毅, 杨俊, 康仪, 等. 异丙酚前药HX0891和HX-0892在大鼠体内的初步药效学评价[J]. 华西药学杂志, 2012, 27(1): 045-047. [42] 张明, 顾为, 张天宏, 等. PSI-6130前药的设计、合成及其在大鼠体内的转化评价[J]. 中国药物化学杂志, 2011, 21(5): 335-344. [43] 黄丽华, 刘志勇, 罗蝉, 等. HPLC-荧光法研究阿德福韦前药的大鼠组织分布[J]. 药物分析杂志, 2011, 31(4): 637-640. [44] 张锦雯, 孙建国, 王广基, 等. 大黄酸在大鼠和比格犬体内的吸收动力学研究[J]. 中国临床药理学与治疗学, 2010, 15(5): 511-518. [45] Peng Y, Sun JG, Wang GJ.Pharmacokinetic study of Rhein and its carboxyl-esterification derivatives in rats[J]. Chin J Nat Med, 2009, 7(3): 228-233. [46] Nicolas P, Tod M, Padoin C, et al.Clinical Pharmacokinetics of Diacerein[J]. Clin Pharmacokinet, 1998, 35(5): 347-359. |