[含有-外毒素的细菌杀虫制剂的急性毒性]。

Problemi na khigienata Pub Date : 1993-01-01
Zh Khalkova, Kh Zaĭkov, G Antov, S Dinoeva
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引用次数: 0

摘要

在含有0.1% β -外毒素的苏云金芽孢杆菌的基础上,通过口服、皮肤、吸入和腹腔注入实验动物,确定了一种新的保加利亚生物杀虫剂制剂的急性毒性。毒性评估是根据世界卫生组织和美国研究植物保护微生物剂安全性的标准,通过综合的毒物计量学、积分学、血液学和病理解剖学方法进行的。已经确定该制剂口服剂量为10,000 mg。kg-1 (1.6.10(11) cell kg)。-1 10微克。Kg-1 β外毒素),皮肤应用剂量为6000毫克。Kg-1(9.6.10(10), 6微克。Kg-1 β外毒素),浓度为300毫克。M-3(4.8.10(10)细胞M-3, 300微克。M-3 β外毒素)在试验动物的整体、血液学和病理解剖研究中不会引起致死性、中毒和变化。雄性大鼠腹腔注射的LD50为387.20毫克(6.2.10(10)kg-1, 387.2微克kg-1 β外毒素),雌性动物为364.0毫克kg-1 (0.58.10(9) kg-1 364.0微克kg-1 β外毒素)。调查指出,根据急性毒性率,含有0.1% β外毒素的细菌制剂是指低毒物质,在遵守生产和使用规定的情况下,不存在急性口服、皮肤和吸入中毒的危险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The acute toxicity of a bacterial insecticidal preparation containing a beta-exotoxin].

The acute toxicity of a new Bulgarian bioinsecticide preparation is determined, produced on the basis of Bacillus thuringiensis containing 0.1% beta-exotoxin by oral, dermal, inhalational and intraperitoneal introduction in experimental animals. The evaluation of the toxicity is performed by a complex of toxicometric, integral, haematologic and pathologicoanatomic methods according to the WHO and USA criteria for studying the safety of the microbic agents for plant protection. It is already established that the preparation introduced orally in dose 10,000 mg.kg-1 (1.6.10(11) cell kg.-1 10 micrograms.kg-1 beta exotoxin), applied dermally in dose 6000 mg.kg-1 (9.6.10(10), 6 micrograms.kg-1 beta exotoxin) and in concentration 300 mg.m-3 (4.8.10(10) cell m-3, 300 micrograms.m-3 beta exotoxin) provokes no lethality, intoxication and changes in the integral, haematologic and pathologicoanatomic studies of test animals. LD50 at intraperitoneal introduction in white rats is 387.20 mg (6.2.10(10), kg-1, 387.2 micrograms kg-1 beta exotoxin) for male and 364.0 mg kg-1 (0.58.10(9) kg-1 364.0 micrograms kg-1 beta exotoxin) for female animals. The investigations point out that according to rate of acute toxicity the bacterial preparation containing 0.1% beta exotoxin is referred to the low toxic substances and reveals no danger for acute oral, dermal and inhalational poisonings when the regulations for production and use are observed.

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