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首页> 外文期刊>Acta Pharmacologica Sinica >Pharmacokinetics of lansoprazole in Chinese healthy subjects in relation to CYP2C19 genotypes
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Pharmacokinetics of lansoprazole in Chinese healthy subjects in relation to CYP2C19 genotypes

机译:兰索拉唑在中国健康受试者中与CYP2C19基因型的药代动力学

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AIM: To study the kinetic characteristics of lansoprazole in healthy Chinese subjects in relation to CYP2C19 genotype status for the individualized dose regimen of lansoprazole. METHODS: Nine homozygous extensive metabolizers (homo EMs) and 9 poor metabolizers (PMs) were recruited for the study from a total of 70 healthy Chinese volunteers, whose CYP2C19 genotype status was determined by the PCR-RFLP techniques: After a single oral dose of 30 mg lansoprazole capsule, plasma concentrations of lansoprazole were determined with HPLC method. RESULTS: In Chinese subjects, the allele frequencies of the CYP2C19m1 and CYP2C19m2 mutation were 0.35 and 0.07, respectively. The concentration-time curves in the two groups were best fitted to a one-compartment model. In the homo EMs and the PMs groups, the main kinetic parameters were as follows: T_(max) (2.44+-0.85) and (2.33+-0.94) h, C_(max)(1.10+-0.34) and (1.73+-0.56) mg/L, Cl/F (16.55+-6.38) and (3.58+-1) L/h, T_(1/2ke)(1.96+-0.51) and (4.21+-0.53) h, AUC were (3.23+-1.08) and (11.05+-3.23) mg·h·L~(-1). A significant difference in AUC, T_(1/2ke), Cl/F, C_(max) values existed between the two groups (P<0.01). CONCLUSION: CYP2C19 genotype is the major factor to influence the interindividual kinetic variability of lansoprazole. Individualized dose regimen of lansoprazole, based on identification of genotype, can be of great benefit for the reasonable use of this drug.
机译:目的:研究兰索拉唑在个体健康人群中与CYP2C19基因型状况相关的动力学特征。方法:从70名健康的中国志愿者中招募了9个纯合的广泛代谢者(homo EMs)和9个弱代谢者(PMs),通过PCR-RFLP技术确定了他们的CYP2C19基因型状态:用HPLC法测定30mg兰索拉唑胶囊的血药浓度。结果:在中国受试者中,CYP2C19m1和CYP2C19m2突变的等位基因频率分别为0.35和0.07。两组的浓度-时间曲线最适合一室模型。在均质EM和PM组中,主要动力学参数如下:T_(max)(2.44 + -0.85)和(2.33 + -0.94)h,C_(max)(1.10 + -0.34)和(1.73+ -0.56)mg / L,Cl / F(16.55 + -6.38)和(3.58 + -1)L / h,T_(1 / 2ke)(1.96 + -0.51)和(4.21 + -0.53)h,AUC为(3.23 + -1.08)和(11.05 + -3.23)mg·h·L〜(-1)。两组之间的AUC,T_(1 / 2ke),Cl / F,C_(max)值存在显着差异(P <0.01)。结论:CYP2C19基因型是影响兰索拉唑个体间动力学差异的主要因素。兰索拉唑的个体化剂量方案(基于基因型鉴定)对于合理使用该药物可能会大有裨益。

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