CYP450酶与中药代谢相互作用及酶活性测定的研究进展(6)
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[48] Stewart N A， Buch S C， Conrads T P， et al. A UPLC-MS/MS assay of the "Pitsburgh cocktail"：six CYP probe-drug metabolites from human plasma andurine using stable isotope dilution [J]. Analyst， 2011， 136(3)： 605.
[49] Tucker G T， Houston J B， Huang S M. Optimizing drug development： strtegies to assess drug metabolism/transporter interaction potential-toward a consensus [J]. Pharm Res， 2001， 18(8)： 1071.
[50] 胡晓波， 谭蓉. 影响CYP450和P-gp活性的抗菌药物联合用药探讨[J].抗感染药学， 2012， 9(4)： 257.
[51] Palmer J L， Scon R J， Gibson A， et al. An interaction between the cytochrome P450 probe substrates chlorzoxazone (CYP2E1) and midazolam (CYP3A)[J]. Br J Clin Pharmacol， 2001， 52(5)： 555.
[责任编辑 马超一] (陆兔林 苏联麟 季德 顾薇 毛春芹)
[47] Ardjomand W， Kollroser M， Li L， et al. Development and xalidation of a LC-MS/MS method based on a new 96-well Hybrid-SPETM-precipitation technique for quantification of CYP450 substrates metabolitesin ratplasma[J]. Anal bioanal chem， 2011， 400(8)： 2371.
[48] Stewart N A， Buch S C， Conrads T P， et al. A UPLC-MS/MS assay of the "Pitsburgh cocktail"：six CYP probe-drug metabolites from human plasma andurine using stable isotope dilution [J]. Analyst， 2011， 136(3)： 605.
[49] Tucker G T， Houston J B， Huang S M. Optimizing drug development： strtegies to assess drug metabolism/transporter interaction potential-toward a consensus [J]. Pharm Res， 2001， 18(8)： 1071.
[50] 胡晓波， 谭蓉. 影响CYP450和P-gp活性的抗菌药物联合用药探讨[J].抗感染药学， 2012， 9(4)： 257.
[51] Palmer J L， Scon R J， Gibson A， et al. An interaction between the cytochrome P450 probe substrates chlorzoxazone (CYP2E1) and midazolam (CYP3A)[J]. Br J Clin Pharmacol， 2001， 52(5)： 555.
[责任编辑 马超一] (陆兔林 苏联麟 季德 顾薇 毛春芹)