Assay procedure standardization of galotrank tablets
Keywords:
galotrank, medicine, standardization
Abstract
Assay procedure standardization of Galotrunk substance in its tablets was carried out. Optimal concentration of the substance in test and reference solutions for UV-spectrophotometry method was defined. Linearity and other metrological characteristics of the procedure were researched. Statistical characteristics are defined.
References
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2. The State Pharmacopoeia of Ukraine. - X .: RIREG, 2001. - 556 p.
3. Technology and standardization of drugs: Sat. scientific tr. / Ed. V.P.Georgievsky, F.A.Konev. - X: Rireg Ltd., 1996. - 784 p.
4. British Pharmacopoeia, 2003.
5. The United States Pharmacopoeia (USP 24). The National Formulary (NF 19). - Philadelphia, 2000. - 2569 p.
6. European Pharmacopoeia Supplement. - 2001.
Published
2020-03-11
How to Cite
Thzurkan, O., Kolyadich, O., Bobkova, L., & Shkliaiev, S. (2020). Assay procedure standardization of galotrank tablets. Farmatsevtychnyi Zhurnal, (2), 58-61. Retrieved from https://pharmj.org.ua/index.php/journal/article/view/846
Section
Original Articles
This work is licensed under a Creative Commons Attribution 4.0 International License.
