Jovanović D, Kovacević V, Maksimović M
Military Technical Institute, Medical Department, Belgrade, Yugoslavia.
Pharmacol Toxicol. 1992 Nov;71(5):340-2. doi: 10.1111/j.1600-0773.1992.tb00558.x.
The pharmacokinetics of the oxime HI-6 from an aqueous solution and from a mixture containing HI-6 and atropine (in doses similar as proposed for their combination in an automatic injector) was studied in German shepherd dogs. A standard manual injection of mixed drugs was followed by enhanced resorption of HI-6 while the elimination curves were quite similar. A comparison of the parameters describing relative bioavailability at the 80% probability level did not reveal any significant differences between the formulations of HI-6. The increase in HI-6 level in blood of animals receiving a mixture is more likely to be attributed to the local vasodilatation than to the systemic cardiovascular effects of atropine.
在德国牧羊犬中研究了肟HI-6在水溶液中以及在含有HI-6和阿托品的混合物(剂量与自动注射器中建议的组合剂量相似)中的药代动力学。对混合药物进行标准手动注射后,HI-6的吸收增强,而消除曲线相当相似。在80%概率水平下对描述相对生物利用度的参数进行比较,未发现HI-6不同制剂之间有任何显著差异。接受混合物的动物血液中HI-6水平的升高更可能归因于局部血管舒张,而非阿托品的全身心血管效应。