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与细胞色素P_(450)2D6相关的药物相互作用研究 被引量:11

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出处 《中国药房》 CAS CSCD 北大核心 2008年第29期2300-2302,共3页 China Pharmacy
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  • 1李菲,程泽能.与细胞色素P_(450)1A2相关的药物相互作用[J].中国药房,2002,13(9):568-569. 被引量:15
  • 2Von Moltke LL, Greenblatt DJ, Duan SX, et al. Inhibition of desipramine hydroxylation (Cytochrome P450- 2D6) in vitro by quinidine and by viral protease inhibitors relation to drug interactions in vivo[J] . Pharm Sci, 1998, 87(10) : 1 184.
  • 3Sproule BA, Naranjo CA, Brenmer KE, et al. Selective serotonin reuptake inhibitors and CNS drug interactions.A critical review of the evidence[J] .Clin Phar macokinet, 1997,33(6) ~ 454.
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  • 5Suzuki Y, Someya T, Shimoda K, et al. Importance of cytochrome P450 2D6 genotype for the drug metabolic interaction between chlorpromazine and haloperidol[J]. Ther Drug Monit , 2001,23(4) : 363.
  • 6Daniel WA,Wojcikowski J .The role of lysosomes in the cellular distribution of thioridazine and potential drug interactions[J] . Toxicol Appl Pharmacol , 1999, 158 (2):115.
  • 7Spina E, Avenoso A, Facciola G,et al. Effect of fluoxetine on the plasma concentrations of clozapine and its major metabolites in patients with schizophrenia[J] . Clin Psychopharmacol, 1998,13(3) .. 141.
  • 8Bork JA, Rogers T, Wedlund PJ, et al. A pilot study on risperidone metabolism: The role of eytoehromesP450 2D6 and 3A[J ] .J Clin Psychiatry, 1999,60(7) : 469.
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  • 10Leibovitz A, Bilchinsky T, Gil I, et al. Elevated serum digoxin level associated with coadministered fluoxetine [J ] .Arch Intern ivied, 1998,158(10): 1 152.

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