[An experimental evaluation of the cutaneous action of the preparation Bulmektin].

Problemi na khigienata Pub Date : 1994-01-01
Zh Khalkova
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Abstract

The acute and subacute dermal toxicity, skin irritating and sensitizing effect of the preparation "Bulmektin" was examined for a period of 21 days. It contains 0.5% active substance Ivermectin. The experiments were carried out in conformity with the Bulgarian State Standards and the OECD methodical recommendations. The unrepeated dermal application of the preparation in dose 6000 mg/kg-1 for white rats provoked no lethality and signs of intoxication. No cumulative effect was established at the 21-day dermal toxicity. The threshold dose is 2000 mg/kg-1. On the basis of the investigations could be accepted, that the preparation carries no danger for acute and chronic dermal intoxications at observing the regulations for its production and use. No local irritation of the skin is established in rats and guinea pigs from the preparation. There is no development of contact allergy at the application of induced and allowed dose of 25% aqua suspension of the preparation on white guinea pigs.

[布美克汀制剂皮肤作用的实验评价]。
观察布美克汀制剂的急性和亚急性皮肤毒性、皮肤刺激和致敏作用,为期21天。含有0.5%的活性物质伊维菌素。实验是按照保加利亚国家标准和经合发组织有条不紊的建议进行的。该制剂以6000 mg/kg-1剂量不重复皮肤给药,对大鼠无致死性和中毒症状。在21天的皮肤毒性试验中未发现累积效应。阈值剂量为2000 mg/kg-1。根据调查,可以接受的是,在遵守其生产和使用规定时,该制剂没有急性和慢性皮肤中毒的危险。该制剂未在大鼠和豚鼠中建立局部皮肤刺激。在白豚鼠身上应用诱导剂量和允许剂量的25%水悬浮液,未发生接触性过敏。
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