[Takal药物组毒性和累积性的比较评价]。

Problemi na khigienata Pub Date : 1994-01-01
A Mikhaĭlova, Zh Khalkova, G Antov, Kh Zaĭkov, N Shumkov
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引用次数: 0

摘要

研究了具有杀菌和抗病毒活性的新剂型“Takal 9”、“Takal 14”和“Takal 16”对实验动物的急性口服毒性和皮肤毒性,以及亚急性口服毒性[连续30天]和皮肤刺激作用。进行了复杂的毒理学、非特异性、血液学、生化和组织学研究。组合物“Takal 9”、“Takal 14”和“Takal 16”在口服和皮肤应用时具有轻微毒性。“Takal 9”和“Takal 16”的LD50在15,000 mg/kg-1以上,而制剂“Takal 14”未达到LD50。在不重复皮肤应用时,所检查的制剂组的LD50超过5000mg /kg-1。本产品对皮肤无刺激作用。在30天的口服治疗条件下,没有建立累积效应。在血清指标没有变化的背景下,用乙醇“Takal 9”和“Takal 16”处理的动物肝脏中有氧和无氧氧化被激活。这些偏差很可能是由于乙醇作为溶剂参与了"Takal 9"和"Takal 16"。在实验的基础上,确定了最适合使用的制剂“Takal 14”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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[A comparative evaluation of the toxic and cumulative properties of the Takal drug group].

The acute oral and dermal toxicity was studied as well as subacute oral toxicity [30 successive days] and skin irritating effect on experimental animals of new drug form "Takal 9", "Takal 14" and "Takal 16" with proved bactericidal and virucidal activity. A complex of toxicometric, unspecific, haematological, biochemical and histological studies were performed. The compositions "Takal 9", "Takal 14" and "Takal 16" are slightly toxic at oral and dermal application. LD50 for "Takal 9" and "Takal 16" is above 15,000 mg/kg-1 while for preparation "Takal 14" is not reached. At unrepeated dermal application LD50 for the examined group of preparations surpasses 5000 mg/kg-1. The products have no skin-irritative effect. No cumulative effect is established in the conditions of a 30-day oral treatment. On the background of no changes in the serum indices an activation of the aerobic and anaerobic oxidation in the liver is registered in animals treated with ethyl alcohol, "Takal 9" and "Takal 16". These deviations are due, most probably, to the participation of ethyl alcohol as solvent, in "Takal 9" and "Takal 16". On the basis of the experiments, as most suitable for use, is established the preparation "Takal 14".

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