贾正平, 徐丽婷, 王冬梅, 谢景文. 高效液相色谱法测定4-4″-(2″,2″,6″,6″-四甲基哌啶氮氧自由基)氨基-4'-去甲表鬼臼毒素大鼠血浆浓度及药代动力学参数J. 药学学报, 1995, 30(10): 768-772.
引用本文: 贾正平, 徐丽婷, 王冬梅, 谢景文. 高效液相色谱法测定4-4″-(2″,2″,6″,6″-四甲基哌啶氮氧自由基)氨基-4'-去甲表鬼臼毒素大鼠血浆浓度及药代动力学参数J. 药学学报, 1995, 30(10): 768-772.
ZP Jia, LT Xu, DM Wang , JW Xie, . HPLC DETERMINATION OF 4-4"(2",2",6",6",TETRAMETHYL-1"-PIPERIDINYLOXY)AMINO-4'-DEMETHYLEPIPODOPHYLLOTOXIN IN RAT PLASMA AND STUDIES OF ITS PHARMACOKINETICSJ. Acta Pharmaceutica Sinica, 1995, 30(10): 768-772.
Citation: ZP Jia, LT Xu, DM Wang , JW Xie, . HPLC DETERMINATION OF 4-4"(2",2",6",6",TETRAMETHYL-1"-PIPERIDINYLOXY)AMINO-4'-DEMETHYLEPIPODOPHYLLOTOXIN IN RAT PLASMA AND STUDIES OF ITS PHARMACOKINETICSJ. Acta Pharmaceutica Sinica, 1995, 30(10): 768-772.

高效液相色谱法测定4-4″-(2″,2″,6″,6″-四甲基哌啶氮氧自由基)氨基-4'-去甲表鬼臼毒素大鼠血浆浓度及药代动力学参数

HPLC DETERMINATION OF 4-4"(2",2",6",6",TETRAMETHYL-1"-PIPERIDINYLOXY)AMINO-4'-DEMETHYLEPIPODOPHYLLOTOXIN IN RAT PLASMA AND STUDIES OF ITS PHARMACOKINETICS

  • 摘要: 建立了大鼠血浆中4-4″-(2″,2″,6″,6″-四甲基哌啶氮氧自由基)氨基-4'-去甲表鬼臼毒素(GP-7)浓度的HPLC测定方法。用ODS柱分离,甲醇-水-冰醋酸(59:41:0.6)为流动相,检测波长285nm。血浆甲乙醚-二氯甲烷混合液萃取,45℃水浴蒸干,残渣用流动相溶解进样,内标法定量;血药浓度在2~200μg·ml-1范围内呈线性关系,r=0.9997,血浆最低检测浓度0.2μg·ml-1,方法回收率94%~100%,日内、日间RSD2.29%~7.70%。大鼠ivGP-710,20,30mg·kg-1,药代动力学过程符合二室开放模型,消除半衰期为39.8±10.8min。

     

    Abstract: 4-4″-(2″,2″,6″,6″-tetramethyl-1″-piperidinyloxy)amino-4'-demethylepipo-dophyllotoxin (GP-7) is a new podophyllotoxin spin-labeled derivative.Its primary effect is theantitumor activity on transplanted mouse tumors and cultured tumor cells. This paper describes amethod for its determination using HPLC with UV detection and the determination of itspharmacokinetic parameters in rats.A Shimadzu LC-6A liquid chromatograph equipped with a Shimadzu SPD-6AV multiwavelengthdetector and a Chromatopac C-R3A data processor was used.The separation was performed on aZorbax-ODS column(5μm,4.6 mm×150 mm) with a mobile phase of methanol-water-glacialacetic acid(59:41:0.6).The flow-rate was 1.0 ml· min-1 and detection was made at 285 nm.A plasma specimen(0.2 ml) was spiked with 22.6μg· ml-1 internal standard(podophyllic acidpiperidinyl hydrazone nitroxide radical, GP-1) and extracted with ether-dichloromethane(3:1).The extract was evaporated at 45℃. The residue was taken up with 0.1 ml of the mobile phase and20μl aliquots were injected into the system.The calibration curve was linear in the range from 2 to 200μg·ml-1 with r=0.9997. Thedetection limit was 0.2 μg· ml-1 and the recovery of GP-7 from rat plasma was 94.3%~100.9%.The relative standard deviations for within-day and between-day were 2.29%~4.64%and5.55%~7.70%, respectively.After iv injection of GP-7 10,20 and 30 mg· kg-1,the concentrations of the drug in ratplasma were determined.The pharmacokinetic parameters of GP-7 were obtained by using MCPKPprogram on a COMPAC-486 computer. The data obtained fitted a two-compartment open model, andthe mean T1/2βvalue was 39.8±10.8 min.

     

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