大剂量口服白消安在异基因造血干细胞移植预处理患者体内药动学研究

张善堂 ;孙自敏 ;刘会兰 ;方焱 ;耿良权 ;唐丽琴 ;吴云 ;谯川南 ;屈建

中国药学杂志 ›› 2009, Vol. 44 ›› Issue (18) : 1416-1419.

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中国药学杂志 ›› 2009, Vol. 44 ›› Issue (18) : 1416-1419.
论文

大剂量口服白消安在异基因造血干细胞移植预处理患者体内药动学研究

  • 张善堂 a ,孙自敏 b* ,刘会兰 b ,方焱 a ,耿良权 b ,唐丽琴 a ,吴云 b ,谯川南 b ,屈建 a
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Pharmacokinetics of Oral Busulfan in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

  • ZHANG Shan-tanga , SUN Zi-minb* , LIU Hui-lanb , FANG Yana , GENG Liang-quanb , TANG Li-qina , WU Yunb , QIAO Chuan-nanb , QU Jiana
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摘要

目的 研究异基因造血干细胞移植( allo-HSCT )预处理患者口服大剂量白消安 (Bu) 的药动学特征。 方法 allo-HSCT 预处理患者口服 Bu 1 mg· kg-1 , q6h ,共 16 剂。在首剂和第 9 剂给药时,分别于给药前及给药后不同时间点采集血样,用高效液相色谱法测定血浆 Bu 浓度;用 DAS 软件进行药动学房室模型拟合,计算药动学参数。 结果 首剂和第 9 剂给药后 Bu 在 allo-HSCT 预处理患者体内血药浓度 - 时间曲线均符合一室模型,其主要药动学参数分别为: <> t 1/2 ( 133.0 ± 30.6) 与 (131.4 ± 28.2)min , <> K e ( 0.005 ± 0.001 )与( 0.006 ± 0.001 ) min-1<> V d /<>F ( 0.56 ± 0.12 )与( 0.46 ± 0.08 ) L·kg-1<> CL /<>F ( 0.003 ± 0.001 )与( 0.002 ± 0.001 ) L·min-1·kg-1 , AUC0-t ( 910.3 ± 146.9 )与( 1 158.5 ± 139.0 ) μmol·min·L-1 , AUC0- ( 1 401.9 ± 243.2 )与 ( 1 689.0 ± 312.4 ) μmol·min·L-1 ; Bu 平均稳态血浆浓度为( 3.29 ± 0.39 ) μmol·L-1 。 结论 口服大剂量 Bu 在 allo-HSCT 预处理患者体内过程符合一室药动学模型,主要药动学参数个体差异大,多次给药后药物清除率发生改变。

Abstract

OBJECTIVE To study the pharmacokinetic profiles of oral busulfan in Chinese patients undergoing allogeneic hematopoietic stem cell transplantation. METHODS Blood samples of 9 adult patients were collected following the first and the ninth dose of standard 16 doses of oral busulfan,4-day regimen. The plasma concentrations of busulfan were determined by HPLC, and the pharmacokinetic parameters of busulfan were calculated by DAS statistical software. RESULTS The plasma concentration- time curves after dose 1 and dose 9 of oral 1 mg·kg-1 busulfan in 9 patients were described by an one-compartment model,respectively. The main pharmacokinetic parameters were as follows:t1/2 (133.0±30.6)and(131.4±28.2)min, Ke (0.005±0.001)and(0.006±0.001)min-1, Vd/F(0.56±0.12)and(0.46±0.08)L·kg-1, CL/F(0.003±0.001)and(0.002±0.001)L·min-1·kg-1, AUC0-t(910.3±146.9)and(1 158.5±139.0)μmol·min·L-1, AUC0-∞(1 401.9±243.2)and(1 689.0±312.4) μmol·min·L-1,respectively. Busulfan average steady state plasma concentration was (3.29±0.39)μmol·L-1. CONCLUSION The pharmacokinetic profiles of oral busulfan are fitted to an one-compartment model,and the main pharmacokinetic parameters are significant difference between dose 1 and dose 9.

关键词

白消安 / 异基因造血干细胞移植

Key words

busulfan / allogeneic hematopoietic stem cell transplantation / preparative regimen / pharmacokinetics

引用本文

导出引用
张善堂 ;孙自敏 ;刘会兰 ;方焱 ;耿良权 ;唐丽琴 ;吴云 ;谯川南 ;屈建 . 大剂量口服白消安在异基因造血干细胞移植预处理患者体内药动学研究[J]. 中国药学杂志, 2009, 44(18): 1416-1419
ZHNG Shn-tng;SUN Zi-min;LIU Hui-ln;FNG Yn;GENG Ling-qun;TNG Li-qin;WU Yun;QIO Chun-nn;QU Jin . Pharmacokinetics of Oral Busulfan in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation[J]. Chinese Pharmaceutical Journal, 2009, 44(18): 1416-1419

参考文献


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( 收稿日期 : 2008-12-11 )


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