[1] Olsson, A.G.; McTaggart, F.; Raza, A. Rosuvastatin: a highly effective new HMG-CoA reductase inhibitor. Cardiovasc. Drug. Rev. 2002, 20, 303-328.
[2] Vaughan, C.J; Gotto, A.M.Jr.; Basson, C.T. The evolving role of statins in the management of atherosclerosis. J. Am. Coll. Cardiol. 2000, 35, 1-10.
[3] Carswell, C.I.; Plosker, G.L.; Jarvis, B. Rosuvastatin. Drugs. 2002, 62, 2075-2085; discussion 2086-2077.
[4] McKenney, J.M. Efficacy and safety of rosuvastatin in treatment of dyslipidemia. Am. J. Health. Syst. Pharm. 2005, 62, 1033-1047.
[5] Martin, P.D.; Warwick, M.J.; Dane, A.L.; Hill, S.J.; Giles, P.B.; Phillips, P.J.; Lenz, E. Metabolism, excretion, and pharmacokinetics of rosuvastatin in healthy adult male volunteers. Clin. Ther. 2003, 25, 2822-2835.
[6] Cooper. K.J.; Martin, P.D.; Dane, A.L.; Warwick, M.J.; Raza, A.; Schneck, D.W. Lack of effect of ketoconazole on the pharmacokinetics of rosuvastatin in healthy subjects. Br. J. Clin. Pharmacol. 2003, 55, 94-99.
[7] Cooper, K.J.; Martin, P.D.; Dane, A.L.; Warwick, M.J; Raza. A.; Schneck, D.W. The effect of erythromycin on the pharmacokinetics of rosuvastatin. Eur. J. Clin. Pharmacol. 2003, 59, 51-56.
[8] Cooper, K.J.; Martin, P.D.; Dane, A.L.; Warwick, M.J.; Schneck, D.W.; Cantarini, M.V. Effect of itraconazole on the pharmacokinetics of rosuvastatin. Clin. Pharmacol. Ther. 2003, 73, 322-329.
[9] Martin, P.D.; Kemp, J.; Dane, A.L.; Warwick, M.J.; Schneck, D.W. No effect of rosuvastatin on the pharma-cokinetics of digoxin in healthy volunteers. J. Clin. Pharmacol. 2002, 42, 1352-1357.
[10] Jindal, D.; Tandon, M.; Sharma, S.; Pillai, K.K. Pharma-codynamic evaluation of warfarin and rosuvastatin co-administration in healthy subjects. Eur. J. Clin. Pharmacol. 2005, 61, 621-625.
[11] Martin, P.D.; Dane, A.L.; Schneck, D.W.; Warwick, M.J. An open-label, randomized, three-way crossover trial of the effects of coadministration of rosuvastatin and fenofibrate on the pharmacokinetic properties of rosuvastatin and fenofibric acid in healthy male volunteers. Clin. Ther. 2003, 25, 459-471.
[12] Cooper, K.J.; Martin, P.D.; Dane, A.L.; Warwick, M.J.; Schneck, D.W.; Cantarini, M.V. The effect of fluconazole on the pharmacokinetics of rosuvastatin. Eur. J. Clin. Pharmacol. 2002, 58, 527-531.
[13] Hsiang, B.; Zhu, Y.; Wang, Z.; Wu, Y.; Sasseville, V.; Yang, W.P.; Kirchgessner, T.G. A novel human hepatic organic anion transporting polypeptide (OATP2). Identification of a liver-specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl-CoA reductase inhibitor transporters. J. Biol. Chem. 1999, 274, 37161-37168.
[14] Nakai, D.; Nakagomi, R.; Furuta, Y.; Tokui, T.; Abe, T.; Ikeda, T.; Nishimura, K. Human liver-specific organic anion transporter, LST-1, mediates uptake of pravastatin by human hepatocytes. J. Pharmacol. Exp. Ther. 2001, 297, 861-867.
[15] Shitara, Y.; Itoh, T.; Sato, H.; Li, A.P.; Sugiyama, Y. Inhibition of transporter-mediated hepatic uptake as a mechanism for drug-drug interaction between cerivastatin and cyclosporine A. J. Pharmacol. Exp. Ther. 2003, 304, 610-616.
[16] Brown, C.D.A.; Windass, A.; Bleasby, K.; Lauffart, B. Rosuvastatin is a high affinity substrate of hepatic organic anion transporter OATP-C. Atheroscler. Suppl. 2001, 2, 90.
[17] Schneck, D.W.; Birmingham, B.K.; Zalikowski, J.A.; Mitchell, P.D.; Wang, Y.; Martin, P.D.; Lasseter, K.C.; Brown, C.D.; Windass, A.S.; Raza, A. The effect of gemfibrozil on the pharmacokinetics of rosuvastatin. Clin. Pharmacol. Ther. 2004, 75, 455-463.
[18] Kosoglou, T.; Statkevich, P.; Yang, B.; Suresh, R.; Zhu, Y.; Boutros, T.; Maxwell, S.E.; Tiessen R.; Cutler, D.L. Pharmacodynamic interaction between ezetimibe and rosuvastatin. Curr. Med. Res. Opin. 2004, 20, 1185-1195.
[19] Simonson. S.G.; Raza, A.; Martin, P.D.; Mitchell, P.D.; Jarcho, J.A.; Brown, C.D.; Windass, A.S.; Schneck, D.W. Rosuvastatin pharmacokinetics in heart transplant recipients administered an antirejection regimen including cyclosporine. Clin. Pharmacol. Ther. 2004, 76, 167-177.
[20] Hatorp, V. Clinical pharmacokinetics and pharmacodynamics of repaglinide. Clin. Pharmacokinet. 2002, 41, 471-483.
[21] Ramanjireddy, T.; Dhachinamoorthi, D.; Chandrasekhar, K.B. Pharmacokinetic study of repaglinide floating drug delivery system in rabbits by RP-HPLC method. J. Chin. Pharma. Sci. 2012, 21, 162-168.
[22] Hatorp, V.; Oliver, S.; Su, C.A. Bioavailability of repaglinide, a novel antidiabetic agent, administered orally in tablet or solution form or intravenously in healthy male volunteers. Int. J. Clin. Pharmacol. Ther. 1998, 36, 636-641.
[23] Plum, A.; Müller, L.K.; Jansen, J.A. The effects of selected drugs on the in vitro protein binding of repaglinide in human plasma. Methods Find. Exp. Clin. Pharmacol. 2002, 22, 139-143.
[24] König, J.; Cui, Y.; Nies, A.T.; Keppler, D. A novel human organic anion transporting polypeptide localized to the basolateral hepatocyte membrane. Am. J. Physiol. Gastrointest. Liver Physiol. 2000, 278, 156-164.
[25] Bidstrup, T.B.; Bjørnsdottir, I.; Sidelmann, U.G.; Thomsen, M.S.; Hansen, K.T. CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide. Br. J. Clin. Pharmacol. 2003, 56, 305-314.
[26] Dunn, F.L. Management of dyslipidemia in people with type 2 diabetes mellitus. Rev. Endocr. Metab. Disord. 2010, 11, 41-51.
[27] Nezasa, K.; Higaki, K.; Takeuchi, M.; Nakano, M.; Koike, M. Uptake of rosuvastatin by isolated rat hepatocytes: comparison with pravastatin. Xenobiotica. 2003, 33, 379-388.
[28] Choi, J.H.; Lee, M.G.; Cho, J.Y.; Lee, J.E.; Kim, K.H.; ParkM K. Influence of OATP1B1 genotype on the pharmacokinetics of rosuvastatin in Koreans. Clin. Pharmacol. Ther. 2008, 83, 251-257.
[29] He, J.; Qiu, Z.; Li, N.; Yu, Y.; Lu, Y.; Han, D.; Li, T.; Zhao, D.; Sun, W.; Fang, F.; Zheng, J.; Fan, H.; Chen, X. Effects of SLCO1B1 polymorphisms on the pharmacokinetics and pharmacodynamics of repaglinide in healthy Chinese volunteers. Eur. J. Clin. Pharmacol. 2011, 67, 701-707.
[30] Meier, P.J.; Stieger, B. Bile salt transporters. Annu. Rev. Physiol. 2002, 64, 635-661.
[31] Tamai, I.; Nezu, J.; Uchino, H.; Sai, Y.; Oku, A.; Shimane, M.; Tsuji, A. Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family. Biochem. Biophys. Res. Commun. 2000, 273, 251-260.
[32] Kajosaari, L.I.; Niemi, M.; Neuvonen, M.; Laitila, J.; Neuvonen, P.J; Backman, J.T. Cyclosporine markedly raises the plasma concentrations of repaglinide. Clin. Pharmacol. Ther. 2005, 78, 388-399.
[33] Lau, Y.Y.; Huang, Y.; Frassetto, L.; Benet, L.Z. Effect of OATP1B transporter inhibition on the pharmacokinetics of atorvastatin in healthy volunteers. Clin. Pharmacol. Ther. 2007, 81, 194-204.
[34] Hagenbuch, B.; Meier, P.J. The superfamily of organic anion transporting polypeptides. Biochim. Biophys. Acta. 2003, 1609, 1-18. |