乳内制剂Cephamasten的生物制药及临床药理学研究

Veterinarno-meditsinski nauki Pub Date : 1987-01-01
B Donev, L Dancheva, M Doneva, I Petkov, D Drumev
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引用次数: 0

摘要

通过微生物学、工艺、生物制药、临床药理学等方面的研究,研制出一种乳内应用于哺乳期奶牛、母羊、山羊乳房炎的动物药物配方Cephamasten。其有效成分为头孢氨苄一水合物。Cephamasten的一致性已被证明适合于腹腔内引入。它在奶牛的乳房内具有良好的耐受性,并能迅速释放其中含有的抗生素。在最后一次输注72小时后,经处理的四分之一的牛奶被证明不含头孢氨苄。头孢马司腾在临床前和临床急性乳腺炎的治疗中均显示出较高的疗效。在第一种情况下,每隔24小时进行两次治疗获得最佳结果,在第二种情况下,每隔12小时进行六次治疗(腹腔内引入制剂)获得最佳结果。在广泛性乳腺炎的情况下,根据病情的严重程度,应每隔4-6-12次应用头孢马斯腾,同时频繁挤奶和其他药物的肠外应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Biopharmaceutical and clinico-pharmacological research on the intramammary preparation Cephamasten].

An animal drug formula, Cephamasten, for intramammary application in the treatment of mastitis-affected cows, ewes, and goats in the lactation period was worked out on the base of microbiologic, technologic, biopharmaceutic, and clinico-pharmacologic studies. Its active ingredient was the Pharmachim cephalexin-monohydrate. The consistence of Cephamasten has proved suitable for intracisternal introduction. It is tolerated well within the udder of cows, and it rapidly releases the antibiotic incorporated in it. The milk of the treated quarters has proved free from cephalexin after the 72nd hour of the last infusion. Cephamasten has shown high effectiveness in the treatment both of the preclinical and of the acute clinical mastitis. In the first case best results were obtained with the twofold treatment at a 24-hour interval, and in the second case--with the sixfold treatment at 12-hour intervals (intracisternal introduction of the preparation). In the case of generalized mastitis, in dependence on the severity of the process Cephamasten is to be applied at 4-6-12 intervals along with frequent milking and the parenteral application of other agents.

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