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去甲斑蝥素脂质微球注射液Beagle犬连续静脉给药90d毒动学研究
Toxicokinetics of norcantharidin lipid microsphere for injection in Beagle’s dog following 90 d repeated iv administration
【摘要】 目的对比研究去甲斑蝥素脂质微球注射液(NCTD-LM)和去甲斑蝥酸钠注射液(NCTD-I)连续90 d静脉滴注给予Beagle犬的毒动学特征,并研究毒性剂量下2种制剂在Beagle犬体内的蓄积情况。方法应用超高效液相色谱-质谱联用(UPLC-MS/MS)法测定各组Beagle犬在首次给药、连续给药44和90 d的血药浓度,并计算毒动学参数。结果分别静脉滴注给予Beagle犬0.8、1.6和3.2 mg/kg NCTD-LM后,首次给药后AUC0-t分别为(2.22±0.53)、(4.77±1.13)和(13.4±3.6)h·mg/L,t1/2分别为(1.37±0.18)、(1.64±0.42)和(1.98±0.25)h;90 d后其AUC0-t分别为(3.58±0.95)、(11.4±2.0)和(23.5±3.9)h·mg/L,t1/2分别为(3.87±1.90)、(5.75±3.29)和(5.84±2.45)h;2.4 mg/kg静脉滴注给予Beagle犬NCTD-I后,首次给药和90 d后其血浆AUC0-t分别为(9.07±2.09)和(14.1±3.0)h·mg/L,t1/2分别为(2.84±1.34)和(3.53±1.26)h。但各组动物在停药15和30 d后,血药浓度均低于定量下限。结论 NCTD-LM在Beagle犬体内0.8~3.2 mg/kg剂量内呈现非线性药动学特征。2种制剂连续静脉给予Beagle犬90 d,血药浓度、AUC0-t和t1/2均随给药时间延长而显著增加,但无长期蓄积作用。
【Abstract】 Objective To evaluate the toxicokinetics and in vivo accumulation of norcantharidin lipid microsphere for injection(NCTD-LM) in Beagle’s dogs following 90 d repeated iv administration by comparing with sodium demethylcantharidate injection(NCTD-I). Methods An ultra high performance liquid chromatography-tandem mass spectrum method was employed to determine the NCTD in plasma of Beagle’s dog after 1, 44, and 90 d repeated iv administration. The toxicokinetic parameters were calculated from the plasma concentration. Results After the first iv administration of 0.8, 1.6, and 3.2 mg/kg NCTD-LM to Beagle’s dog, the AUC0-t were(2.22 ± 0.53),(4.77 ± 1.13), and(13.43 ± 3.64) h·mg/L, respectively, while the t1/2 were(1.37 ± 0.18),(1.64 ± 0.42), and(1.98 ± 0.25) h, respectively. After the 90 d repeated iv administration of 0.8, 1.6 and 3.2 mg/kg NCTD-LM to Beagle’s dog, the AUC0-twere(3.58 ± 0.95),(11.4 ± 2.0), and(23.5 ± 3.9) h·mg/L, respectively, while the t1/2 were(3.87 ± 1.90),(5.75 ± 3.29), and(5.84 ± 2.45) h, respectively. For NCTD-I, the AUC0-t were(9.07 ± 2.09) and(14.1 ± 3.0) h·mg/L respectively after 1 and 90 d repeated iv administration, while the t1/2 were(2.84 ± 1.34) and(3.53 ± 1.26) h. 15 and 30 d after the end of administration, the concentration of NCTD in plasma of Beagle’s dog in each group were all dropped below the lowest limit of quantification(LLOQ). Conclusion NCTD displays a nonlinear elimination at the dose range of 0.8—3.2 mg/kg after iv administration of NCTD-LM to Beagle’s dog. Over the 90 d repeated iv administration period, the plasma concentration levels, AUC0-t, and t1/2 for both NCTD-LM and NCTD-I are increased with time increasing. However, no accumulation of NCTD is observed for the both formulations.
【Key words】 NCTD-LM; NCTD-I; Beagle’s dog; toxicokinetics; nonlinear pharmacokinetics; UPLC-MS/MS;
- 【文献出处】 中草药 ,Chinese Traditional and Herbal Drugs , 编辑部邮箱 ,2015年23期
- 【分类号】R285.1
- 【下载频次】238