Procedure of matter identification of reference material for composition of azithromycin with use of spectral method
https://doi.org/10.20915/2687-0886-2021-17-3-21-34
Abstract
In new medicinal products development, as well as actualisation of assessment approaches of medicinal products in circulation, the development of quality control procedures remains one of the most important issues in standardisation. Besides, such development should include using reliable, accurate and sensitive physicochemical methods which determine the need development and implementation of reference materials. This paper discusses the development of reliable methods for identifying the structure of azithromycin, which will guarantee the purity of the reference material, as well as adequately and unambiguously choose a method of quantitative determination in accordance with the current requirements of regulatory acts, and according to the Pharmacopoeia of the Russian Federation of the XIV Edition.
About the Authors
V. I. GegechkoriRussian Federation
Vladimir I. Gegechkori, PhD (Farm.), associate professor of the department of pharmaceutical and toxicological chemistry A. P. Arzamastsev institute of pharmacy A. P. Nelyubin
ResearcherID AAD-2259-2019
13 Nikitsky blvd., building 1, Moscow, 121019
N. A. Shulga
Russian Federation
Nikolai A. Shulga, aboratory assistant at the Department of Pharmaceutical and Toxicological Chemistry named after A. P. Arzamastsev Institute of Pharmacy. A. P. Nelyubin
13 Nikitsky blvd., building 1, Moscow, 121019
O. Iu. Shchepochkina
Russian Federation
Olga Iu. Shchepochkina, PhD (Farm.), associate professor of
the department of pharmaceutical and toxicological chemistry A. P. Arzamastsev institute of pharmacy A. P. Nelyubin
13 Nikitsky blvd., building 1, Moscow, 121019
N. V. Gorokhovets
Russian Federation
Neonila V. Gorokhovets, PhD (Biol.), leading researcher, laboratory of molecular biology and biochemistry
8 Trubetskaya str., bldg. 2, Moscow
A. A. Levko
Russian Federation
Anatolii A. Levko, PhD (Med.), deputy head of the department for inspection of production of medicines and expertise
6 Lavrov lane, Moscow, 109044
N. N. Chadova
Russian Federation
Nataliia N. Chadova, PhD (Chem.), head of the department for inspection of production of medicines and expertise
6 Lavrov lane, Moscow, 109044
V. N. Shestakov
Russian Federation
Vladislav N. Shestakov, director
6 Lavrov lane, Moscow, 109044
References
1. Shchepochkina O. Y., Gegechkori V. I., Prokof’eva V. I., Chepilo D. A., Levko A. A., Chadova N. N., Shestakov V. N. Modern approaches to the development of standard samples of drugs. Pharmaceutical chemistry journal. 2020;54(7):761-765. https://doi.org/10.1007/s11094-020-02267-y
2. Dorofeev V. L., Arzamastsev A. P. Reference samples for pharmacopoeial analysis. Problems of biological, medical and pharmaceutical chemistry. 2010; 8(5): 6-10. (In Russ.).
3. GOST R ISO 9001-2015 Quality management systems. Requirements. Moscow: Standartinform; 2020. (In Russ.).
4. GOST ISO Guide 35-2015 Reference materials. General and statistical principles for certification. Moscow: Standartinform; 2016. (In Russ.).
5. Veselov A. V., Kozlov R. S. Azithromycin: modern aspects of clinical application. Clinical microbiology and antimicrobial chemotherapy. 2006; 8(1):18-32. (In Russ.).
6. Exact Mass Calculator, Single Isotope Version. Available at: https://www.sisweb.com/referenc/tools/exactmass.htm? (date of access: 12.01.2021).
7. State Pharmacopoeia of the Union of Soviet Socialist Republics. 10th ed. Moscow: Medicine, 1968. 1079 p. (In Russ.).
8. State Pharmacopoeia of the Russian Federation. XIV ed. Moscow. Available at: http://www.femb.ru (date of access: 12.01.2021).
9. European Pharmacopoeia. 8th Ed. European Department for the Quality of Medicines. Strasbourg, France: European Department for the Quality of Medicines; 2017.
10. British Pharmacopoeia 2016. London: H. M. Stationary Office; 2015. 1276 p.
11. The United States Pharmacopeia 40 - National Formulary 35, Reissue. 2018.
12. Gegechkori V. I., Shchepochkina O. Iu., Pyatin B. M., Grushevskaya L. N. Development of a method for the determination of heavy metals in standard samples of preparations of peptide structure using the method of atomic absorption spectrometry. Natural and technical sciences. 2015;10(88): 201-205. (In Russ.).
13. Gegechkori V. I., Kokorekin V. A., Shchepochkina O. Yu., Piatin B. M., Grushevskaya L. N., Avdunina N. I., Gaevaya L. I. Application of 1H and 13C nmr spectroscopy in the analysis of reference standards of dilept and GB-115, medicinal products of peptide structure. Russian Journal of Biopharmaceuticals. 2016; 8(3): 37-43. (In Russ.).
14. Gegechkori V. I., Shchepochkina O. Yu., Rodionova G. M., Grushevskaya L. N., Piatin B. M. Use of gas chromatography in quality control of reference standards of medicinal products of peptide structure. Russian Journal of Biopharmaceuticals. 2015;7(6):43-48. (In Russ.).
15. GOST ISO Guide 33-2019 Reference materials. Good practice in using reference materials. Moscow: Standartinform; 2019. (In Russ.).
16. ISO/TR10989:2009: Reference materials - Guidance on, and keywords used for, RM categorization. Available at: https://www.iso.org/standard/46526.html
17. Brennan R. J., Barber J. Full assignments of the 13C and 1H NMR spectra of azithromycin in buffered D2O and DMSO-d6. Magnetic resonance in chemistry. 1992; 30(4):327-333. https://doi.org/10.1002/mrc.1260300410
Review
For citations:
Gegechkori V.I., Shulga N.A., Shchepochkina O.I., Gorokhovets N.V., Levko A.A., Chadova N.N., Shestakov V.N. Procedure of matter identification of reference material for composition of azithromycin with use of spectral method. Measurement Standards. Reference Materials. 2021;17(3):21-34. (In Russ.) https://doi.org/10.20915/2687-0886-2021-17-3-21-34

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