Development of industrial production technology with determination of the quality of a soft medicine «Vetmikoderm» for veterinary

Abstract

It is well known, that 1,2,4–triazole derivatives have a wide range of biological properties, showing little toxicity. Original modeling of 1,2,4-triazole derivatives allows obtaining new molecules with unique properties. Such purposeful changes in molecules are popular among many scientists because they make it possible to obtain compounds with «improved» properties. Such a compound was the substance (4-((5-(decylthio)-4-methyl-4H-1,2,4-triazol-3-yl)-methyl)morpholine with the prospect of creating a mild medicinal product – liniment «Vetmikoderm».
 The main advantage of these medicinal forms is a low traumatic effect on damaged tissue, creating maximum contact with the wound surface, etc. It has been proven, that the antimicrobial agents available on the veterinary drugs’ market, including those ones in the form of ointments, gels and liniments, are characterized by the fact that they do not always stimulate tissue regeneration processes. Medicines with the ability to improve wound healing, as a rule, have minor antiseptic properties. Under these circumstances, the search, development and introduction of the medicines that have antimicrobial and antifungal action is an extremely urgent issue of modern veterinary medicine.
 The aim of our research was to study the technological aspects and manufacturing features, the substantiation of the composition, the analysis of the soft medicinal form of the drug «Vetmikoderm».
 During the research, the appearance, transparency, and thickness of the drug were determined. APHI identification was carried out with the determination of its content by the gas chromatography’s method. The external standard method was used. Microbiological purity (bacteria, yeast and mold fungi (in total), the presence of bacteria of the Enterobacteriaceae family, Staphylococcus aureus and Pseudomonas aeruginosa) was determined in accordance with the requirements of the SPHU by the membrane filtration method. Sterile soy–casein agar was used to determine the total number of aerobic bacteria. Determination of harmlessness was carried out according to the «abnormal toxicity» indicator.
 On the basis of the conducted research, the technological aspects and manufacturing features, substantiation of the composition, quantitative and qualitative analysis of the «Vetmikoderm» liniment were determined, which ensures the possibility of the medicinal form’s obtaining in industrial conditions. The proposed methods of the medicinal form’s analysis are characterized by sensitivity and reproducibility.