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[6β-纳曲醇在比格犬单次及多次肌肉注射后的药代动力学]

[Pharmacokinetics of 6beta-naltrexol after single and multiple intramuscular injections in Beagle dogs].

作者信息

Yan Ling-Di, Liu Jun, Dong Hua-Jin, Cui Meng-Xun, Yao Xia-Jun, Liu Yong-Shao, Gong Zheng-Hua, Gong Ze-Hui

机构信息

Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing 100850, China.

出版信息

Yao Xue Xue Bao. 2009 Jul;44(7):722-5.

Abstract

The pharmacokinetics of 6beta-naltrexol (6beta-NOL) following single intramuscular administration and multiple intramuscular injection once per day for seven days was studied in 4 Beagle dogs. Plasma concentration of 6beta-NOL in dogs was analyzed by a combination of high performance liquid chromatography (HPLC) and electrochemical detection with naloxone (NLX) as internal standard. After single intramuscular injection of 0.2 mg x kg(-1) 6beta-NOL, the plasma concentration-time curve of the drug was found to fit to a two compartment model with first-order absorption. The main parameters of single dosing were as follows: t1/2alpha was (0.26 +/- 0.23) h, t1/2beta was (4.77 +/- 1.65) h, C(max) was (81.65 +/- 5.61) ng x mL(-1), t(peak) was (0.27 +/- 0.07) h, CL(s) was (1.20 +/- 0.06) L x kg(-1) x h(-1), V/F(c) was (1.94 +/- 0.15) L x kg(-1), and AUC(0-t) was (166.82 +/- 7.68) ng x h x mL(-1), separately. After multiple intramuscular injection of 0.2 mg x kg(-1) 6beta-NOL once per day for seven days, the plasma concentration-time curve of the drug fitted to a two compartment model with first-order absorption too. The main parameters of the last dosing were as follows: t1/2alpha was (0.19 +/- 0.18) h, t1/2beta was (5.79 +/- 1.50) h, C(max) was (79.82 +/- 10.5) ng x mL(-1), t(peak) was (0.18 +/- 0.08) h, CL(s) was (1.12 +/- 0.07) L x kg(-1) x h(-1), V/F(c) was (2.10 +/- 0.27) L x kg(-1), and AUC(0-t) was (173.23 +/- 9.49) ng x h x mL(-1), separately. The difference of the parameters between the first and the last dosing was not significant, showing that the plasma kinetics of 6beta-naltrexol was not changed after multiple administrations. In the course of multiple administration, the peak and valley concentration of plasma 6beta-naltrexol were (79.03 +/- 10.3) and (1.50 +/- 0.93) ng x mL(-1), respectively. No clear adverse events were noted during this study. These results showed that plasma 6beta-naltrexol fits to a two compartment model with first-order absorption in dog after intramuscular administration and their pharmacokinetic parameters were reported. There was no remarkable change on plasma pharmacokinetics of 6beta-naltrexol after multiple intramuscular administrations.

摘要

在4只比格犬中研究了单次肌肉注射及连续7天每天一次肌肉注射6β-纳曲醇(6β-NOL)后的药代动力学。以纳洛酮(NLX)为内标,采用高效液相色谱(HPLC)和电化学检测相结合的方法分析犬体内6β-NOL的血浆浓度。单次肌肉注射0.2mg·kg⁻¹ 6β-NOL后,发现该药物的血浆浓度-时间曲线符合一级吸收的二室模型。单次给药的主要参数如下:t1/2α为(0.26±0.23)h,t1/2β为(4.77±1.65)h,C(max)为(81.65±5.61)ng·mL⁻¹,t(peak)为(0.27±0.07)h,CL(s)为(1.20±0.06)L·kg⁻¹·h⁻¹,V/F(c)为(1.94±0.15)L·kg⁻¹,AUC(0-t)为(166.82±7.68)ng·h·mL⁻¹。连续7天每天一次肌肉注射0.2mg·kg⁻¹ 6β-NOL后,该药物的血浆浓度-时间曲线也符合一级吸收的二室模型。末次给药的主要参数如下:t1/2α为(0.19±0.18)h,t1/2β为(5.79±1.50)h,C(max)为(79.82±10.5)ng·mL⁻¹,t(peak)为(0.18±0.08)h,CL(s)为(1.12±0.07)L·kg⁻¹·h⁻¹,V/F(c)为(2.10±0.27)L·kg⁻¹,AUC(0-t)为(173.23±9.49)ng·h·mL⁻¹。首次给药和末次给药参数之间的差异不显著,表明多次给药后6β-纳曲醇的血浆动力学未发生改变。在多次给药过程中,血浆6β-纳曲醇的峰浓度和谷浓度分别为(79.03±10.3)和(1.50±0.93)ng·mL⁻¹。本研究期间未观察到明显的不良事件。这些结果表明,肌肉注射后犬体内血浆6β-纳曲醇符合一级吸收的二室模型,并报告了其药代动力学参数。多次肌肉注射后6β-纳曲醇的血浆药代动力学无明显变化。

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