1 Tuker GT.The interaction of proton pump inhibitors with cytochromeP450[J].Aliment Pharmacol Ther,1994;8:33-8 2 Rizzo N,Padoin C,Palombo S,Scherrmann JM,Girre C.Omeprazole and lansoprazole are not inducers of cytochrome P4501A2 under conventional therapeutic conditions[J].Eur J Clin Pharmacol,1996;49:491-5 3 Bendriss EK,Markoglou N,Wainer IW.Liquid chromatographic method for the simultaneous determination of caffeine and fourteen caffeine metabolites in urine[J].J Chromatogr B,2000;746:331-8 4 张鉴,彭向前,李军.咖啡因探针法测定正常人肝脏药物代谢酶CYP1A2 活性[J].中国药房,2005;16:1216-8 5 李军,彭向前,张鉴.HPLC 直接进样测定咖啡因代谢物评价3 种药物代谢酶活性[J].中国临床药理学与治疗学,2005;10:768-71 6 李菲,程泽能.与细胞色素P4501A2 相关的药物相互作用[J].中国医院用药评价与分析,2002;2:114-5 7 Hartmann M,Zech K,Bliesath H,Steinijans VW,Koch H,Wurst W,et al.Pantoprazole lacks induction of CYP1A2 activity in man[J].Int J Clin Pharmacol Ther,1999;37:159-64 8 Dilger K,Zheng Z,Klotz U.Lack of drug interaction between omeprazole,lansoprazole,pantoprazole and theophylline[J].Br J Clin Pharmacol,1999;48:438-44 9 董瑞谦,郭瑞臣,曹宇梅,徐炳英,崔秀君.妊娠妇女乙酰化代谢表型的研究[J].中国临床药理学与治疗学,2003;8:304-7 10 曹晓梅,卢建丰,蒋永宏,卓海通,凌树森.咖啡因代谢物AFMU,1 X 的测定及其在N-乙酞化分型中的应用[J].中国药学杂志,1997;32:486-9 11 李东至,林其德,林建华.妊高征患者血中黄嘌呤氧化酶和过氧化脂质水平的变化[J].中国病理生理杂志,2002;18:773-7 |