Influence of ABCB1 gene polymorphisms on the pharmacokinetics of azithromycin among healthy Chinese Han ethnic subjects

被引:31
|
作者
He, Xiao-Jing [1 ]
Zhao, Li-Mei [1 ]
Qiu, Feng [1 ]
Sun, Ya-Xin [1 ]
Jesse Li-Ling [2 ,3 ]
机构
[1] China Med Univ, Dept Pharm, Shengjing Hosp, Shenyang 110004, Peoples R China
[2] China Med Univ, Dept Med Genet, Shenyang 110001, Peoples R China
[3] Northeastern Univ, Sinodutch Biomed & Informat Engn Sch, Shenyang 110003, Peoples R China
关键词
ABCB1; azithromycin; pharmacokinetics; single nucleotide polymorphisim (SNP); MULTIDRUG-RESISTANCE GENE; GENOTYPE-RELATED PHARMACOKINETICS; PRODUCT P-GLYCOPROTEIN; MDR1; GENE; DRUG TRANSPORTERS; DIGOXIN PHARMACOKINETICS; TISSUE DISTRIBUTION; CLARITHROMYCIN; EXPRESSION; PHARMACOGENOMICS;
D O I
10.1016/S1734-1140(09)70140-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to evaluate the effiects of ABCB1 gene polymorphisms on azithromycin pharmacokinetics in Chinese Hall ethnic subjects In total, 20 healthy volunteers with various ABCB1 genotypes (6 with 2677GG/3435CC, 8 with 2677GT/3435CT, 6 with 2677TT/3435TT) were enrolled Each was given a single oral dose of 500 mg azithromycin Plasma concentration was measured for Lip to 96 Ill by LC/MS/MS As shown, C-max was significantly lower among individuals with 2677TT/3435TT genotype (468.0 +/- 173.4 ng . h/ml) than those with 2677GG/3435CC (911.2 +/- 396.4 ng . h/ml, p = 0.013) However, the t(max) value was higher among subjects with 2677TT/3435TT (2.0 +/- 0.5 h) than those with 2677GT/3435CT (1.6 +/- 0.3 h) or 2677GG/3435CC (1.4 +/- 0.4 h) genotypes (p = 0 068 and p = 0 026, respectively) Furthermore, the AUC(last) tended to be higher among subjects with 2677GG/3435CC than those with 2677GT/3435CT or 2677TT/3435TT genotypes (5000.2 +/- 1610.0 vs 4558.0 +/- 805.0 vs. 4131.0 +/- 995.1 ng/ml) Our results showed for the first time that azithromycin pharmacokinetics may be influenced by particular polymorphisms of the ABCR1 gene. Individualized dosage regimen design incorporating such information may improve the efficacy of the drug while reducing adverse reactions
引用
收藏
页码:843 / 850
页数:8
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