兽药“双布他司汀软膏”的药理学研究

O. Katsaraba, R. Sachuk, B. Gutyj, T. Velesyk, M. L. Radzykhovskyi, P. Sharandak, V. Pepko
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引用次数: 2

摘要

外用兽药软膏——“Dibutalastin软膏”的药理学研究是该药临床前研究的必做阶段,是PP“Biopharm”和LLC“DEVIE”的新开发项目。在对实验动物进行的科学实验中,可以评估药物在不同使用期限下的安全性,以确定毒性作用区域和不会对健康造成有害影响的剂量。因此,本研究旨在对该药物与水杨酸甲酯和二甲亚砜一起进行药理学研究,以软膏的形式用于治疗患有乳腺炎、关节炎、肌炎和各种来源损伤的欧洲黇鹿、鹿、狗和猫。在温血动物的“急性”实验中,研究了水杨酸甲酯和二甲亚砜为基础的软膏“双丁胺素”的毒理学特性。由于体积超过允许水平,无法确定灌胃给药的平均致死剂量(LD50)。根据“入胃平均致死剂量”指标,确定该兽药属于相对无毒物质(毒性类IV)。药理学研究结果表明,该兽药不存在吸收毒性作用、致敏性和对眼睛和皮肤粘膜的刺激作用。在研究该药的急性毒性时,对动物器官的病理形态学研究表明,研制的水杨酸甲酯和二甲亚砜软膏不会引起内脏器官的病理改变。从兽药毒理学角度看,该药是安全的。进一步的研究将是注册前试验的下一阶段,旨在研究“双布他汀软膏”的胚胎毒性作用,这是该药品档案中“安全性和残留研究”部分的强制性材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological studies of the veterinary medicinal product “Dibutalastin Ointment”
The study of pharmacological studies of the veterinary medicinal product for external use in the form of ointment – “Dibutalastin Ointment” is a mandatory stage of preclinical research of the drug, which is a new development of PP “Biopharm” and LLC “DEVIE”. In a scientific experiment on laboratory animals, it is possible to assess the drug's safety for different terms of use to determine the zone of toxic action and doses that do not cause harmful effects on health. Therefore, the work aimed to carry out pharmacological studies of the drug with methyl salicylate and dimethyl sulfoxide in the form of an ointment for treating European fallow deer, deer, dogs, and cats with mastitis, arthritis, myositis, and injuries of various origins. The toxicological characteristics of the studied ointment “Dibutalastin” based on methyl salicylate and dimethyl sulfoxide were studied in an "acute" study on warm-blooded animals. The average lethal dose (LD50) for intragastric administration could not be established, as the volume exceeded the permissible level. It was established that according to the “average lethal dose when entering the stomach” indicator, the veterinary medicinal product belongs to relatively non-toxic substances (toxicity class IV). The results of pharmacological studies indicate the absence of resorptive-toxic effects, sensitizing properties, and irritating effects on the mucous membranes of the eyes and skin. Pathomorphological studies of animal organs when studying the acute toxicity of the drug showed that the developed ointment with methyl salicylate and dimethyl sulfoxide does not cause pathological changes in internal organs. From the point of view of veterinary toxicology, this drug is safe. Further studies will be the next stage of pre-registration tests aimed at studying the embryotoxic effect of “Dibutalastin Ointment”, which is mandatory material of the “Safety and residue studies” section of the dossier for this medicinal product.
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