Analysis of combined cream with antifungal activity in terms of «microbiological purity»
Journal Title: Фармацевтичний журнал - Year 2015, Vol 1, Issue 1
Abstract
According to GMP requirements, quality control of medicinal products justifies their safety and effectiveness from the development and production to the consumer. One of the important parameters in the development of a new pharmaceutical drug is its microbiological purity. Therefore, the development and validation of methods of determining the indicator «microbiological purity» as a component of stability of developed drug is obligatory. The aim of the study was to evaluate the microbiological purity of the developed combination soft drug for the treatment of dermatomycosis in different conditions of storage and packaging. The objects of the analysis were samples of the developed cream containing clotrimazole, metronidazole, betamethasone dipropionate and urea. The study of the microbiological purity was conducted according to the requirements of the State Pharmacopoeia of Ukraine. The analysis of the developed cream in terms of «microbiological purity» using deep-sowing method has showed the total aerobic microbial count (TAMC) for each sample: not more than 102 CFU/g; the total combined yeasts/moulds count (TYMC): not more than 10 CFU/g; Staphylococcus aureus and Pseudomonas aeruginosa in 1g have not been found. During the shelf time at 2–25 °C condition cream meets the requirements of the State Pharmacopoeia of Ukraine.
Authors and Affiliations
С. V. Birukova, Aram Dullah, I. O. Vlasenko, L. L. Davtian, Y. V. Voyda
Control of elemental impurities in herbal medicines
The standardisation of plant raw materials is among the most important problems of the production of herbal medicines. Medicinal plant raw materials are of complex nature and can be contaminated with impurity elements. T...
Determination of the cost-effective advantages of regimens of diabetes mellitus type 2 with modern DPP-4 inhibitors
Diabetes mellitus is a medical and social problem. The results of the pharmacoeconomical researches should be considered when choosing a rational pharmacotherapy. The purpose of this research of treatment regimens of di...
Effect of different diluent’s type on trimetazidine dihydrochloride release from matrix tablets
Oral matrix tablets are the modern dosage forms using which could be achieved desirable in vitro release kinetics of active pharmaceutical ingredient (API) and correspondent in vivo concentration level. That’s why the st...
Research of the system of information providing for safe pharmacotherapy pregnancy in the world
Improvement of information provision for safe and rational use of medicines at pregnancy is a priority task for all system of healthcare in the world. The purpose of this study was to analyze and carry out a systematic a...
Optimization of detection range of hydrazides of carboxylic acids and 2-acylhydrazinсarbothioamids by HPLC-ECI-MC
Elaboration of control steps of hydrazids and сarbothioamids, raw materials in the synthesis of 1,2,4-triazol-3-yl-thioacetate acids, potential drug substances on research and production stage is an important task. The...