Please use this identifier to cite or link to this item: http://dspace.nuph.edu.ua/handle/123456789/31625
Title: The study of the stability of silver proteinate solutions prepared in pharmacies
Other Titles: Вивчення стабільності розчинів срібла протеїнату, виготовлених в умовах аптеки
Authors: Cherniakova, V. O.
Bevz, N. Yu.
Strilets, O. P.
Harna, N. V.
Bevz, O. V.
Yevtifieieva, O. A.
Чернякова, В. О.
Бевз, Н. Ю.
Стрилець, О. П.
Гарна, Н. В.
Бевз, О. В.
Євтіфеєва, О. А.
Keywords: extemporaneous dosage forms;titrimetric method of analysis;validation;silver proteinate;chemical stability;microbiological purity;екстемпоральна лікарська форма;титриметричний метод аналізу;валідація;срібла протеїнат;хімічна стабільність;мікробіологічна чистота;протаргол
Issue Date: 2023
Publisher: ScienceRise: Pharmaceutical Science
Bibliographic description (Ukraine): The study of the stability of silver proteinate solutions prepared in pharmacies / V. Cherniakova, N. Bevz, O. Strilets, N. Harna, O. Bevz, O. Yevtifieieva // ScienceRise: Pharmaceutical Science. - 2023. - № 5 (45). - Р. 24-31.
Abstract: Today, medicines made in pharmacies are increasingly attracting consumers’ attention and are in growing demand in Ukraine. Pharmacy production faces a number of problems, including the study of the stability of extemporaneous dosage forms and the determination of an optimal shelf life. 1 % and 2 % water silver proteinate solutions used in ophthalmology, otolaryngology and nephrology are produced in Ukrainian pharmacies both extemporaneously and as a reserve. The aim. The aim of the work is to develop methods for quality support and study the chemical stability of 1 % and 2 % water solutions of silver proteinate, and to study the microbiological purity to extend the storage time of nasal drops. Materials and methods. A study of the chemical stability of 1 % and 2 % water silver proteinate solutions of pharmaceutical production is carried out using chemical identification reactions (to silver and protein), quantitative determination by thiocyanatometric titrimetric method and determination of microbiological purity. Results. The validation characteristics of the method for the quantitative thiocyanatometric determination of sil- ver proteinate were studied (the correlation coefficient r=0.9995 and 0.9996; the systematic error – 0.26 % and 0.03 %, the relative confidence interval – 0.88 % and 0.74 % for 1 % and 2 % solutions, respectively), as well as its suitability for this purpose was proven. “Silver proteinate solution, 1.0 %” and “Silver proteinate solution, 2.0 %” prepared in the pharmacy were studied for 150 days by the “Microbiological purity” indicator and were biologically stable. Conclusions. The chemical identification reactions and methods for the quantitative determination of silver pro - teinate in an extemporaneous dosage form used to study the chemical stability of the drug have been proposed. The study results of the chemical stability and microbiological purity allow us to recommend pharmacies to extend the shelf life of nasal drops containing silver proteinate as an active pharmaceutical ingredient for 150 days
URI: http://dspace.nuph.edu.ua/handle/123456789/31625
Appears in Collections:Наукові публікації кафедри медичної хiмiї

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