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Development and validation of the method for quantitative determination of preservatives in sodium oxybutyrate syrup

https://doi.org/10.29235/1561-8331-2023-59-1-26-34

Abstract

A simple, fast, sensitive method for the determination of preservatives (methyl parahydroxybenzoate, propyl parahydroxybenzoate) in the finished dosage form of sodium oxybutyrate syrup based on the simultaneous determination of preservatives using high performance liquid chromatography (HPLC) is proposed. The HPLC method was validated. The correlation coefficient of the linearity of the technique was 0.999 in the application range of 80–120 % of the normalized value. The calibration graph is linear in the region of 0.495–0.990 mg/ml of methyl 4-hydroxybenzoate and 0.165–0.330 mg/ml of propyl 4-hydroxybenzoate. It has been established that the analytical characteristics of the test procedure (selectivity, linearity, correctness, repeatability, reproducibility) satisfy the selected acceptance criteria.

About the Authors

Z. I. Kuvaeva
Institute of Physical Organic Chemistry of the National Academy of Sciences of Belarus
Belarus

Kuvaeva Zoya I. – D. Sc. (Chemistry), Professor, Head
of the Department

13, Surganov Str., 220072, Minsk



S. P. Kacherskaya
Institute of Physical Organic Chemistry of the National Academy of Sciences of Belarus
Belarus

Kacherskaya Svetlana P. – Head of the thematic group
for the analytical control of medicinal substances

13, Surganov Str., 220072, Minsk



O. S. Mastitskaya
Institute of Physical Organic Chemistry of the National Academy of Sciences of Belarus
Belarus

Mastitskaya Olga S. – Junior Researcher

13, Surganov Str., 220072, Minsk



E. A. Khvalova
Institute of Physical Organic Chemistry of the National Academy of Sciences of Belarus
Belarus

Khvalova Evgeniya A. – Junior Researcher

13, Surganov Str., 220072, Minsk



References

1. Egoshina Yu. A., Potselueva L. A., Galiullina T. N. Auxiliary substances in tablet production. Kazan: KSMU, 2003. 15 p. (in Russian).

2. Bolshakov V. N. Auxiliary substances in the technology of dosage forms. Leningrad, 1991. 48 p. (in Russian).

3. Sheryakova A. A. (ed.). State Pharmacopoeia of the Republic of Belarus. GF RB II. Vol. 1. Molodechno: Pobeda Publ., 2013. 1120 p. (in Russian).

4. Drozd E. A. Parabens: synthesis and application. Nauka – shag v budushchee: tez. dokl. XIV stud. nauch.-prakt. konf., Minsk, 30 noyabrya–4 dekabrya 2020 g. [Science is a step into the future: abstracts of the XIV student scientific and practical conference of the Faculty of Technology of Organic Substances, Minsk, November 30th –December 4th, 2020]. Minsk: BSTU, 2020, pp. 25 (in Russian).

5. Kolosova L. V., Gunar O. V. Efficacies of antimicrobial conservants of various non-sterile medicines for oral use. Pharmaceutical Chemistry Journal, 2015, vol. 49, no. 9, pp. 635–638. https://doi.org/10.1007/s11094-015-1343-4

6. Lebedev A. S., Orlov V. Yu., Petrov A. S. Development of HPLC-UV techniques for quantitative analysis of 4-hydroxybenzoic acid esters (parabens) in foodstuffs, cosmetics and pharmaceutical products. Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya = ChemChemTech, 2019, vol. 63, no. 1, pp. 11–17 (in Russian). https://doi.org/10.6060/ivkkt.20206301.6059

7. Mtsariashvili M. R., Garmonov S. Yu., Nigmatullina R. I., Egorova S. N. Development and validation of a method of determining ambroxol hydrochloride and impurities in syrup with HPLC. Chelovek i ego zdorov'e = Humans and their health, 2016, no. 2, pp. 100–107 (in Russian).

8. TKP 432-2012 (02041). Technical code of practice "Manufacturing of medicines: validation of test methods". Minsk: Department of Pharmaceutical Industry of the Ministry of Health of the Republic of Belarus, 2012. 19 p. (in Russian).

9. Epshtein N. A., Emshanova S. V. Requirements to HPLC systems suitable for quality control of parent substances and dosage forms. Pharmaceutical Chemistry Journal, 2008 vol. 42, no. 11, pp. 637–643. https://doi.org/10.1007/s11094-009-0194-2

10. Kiseleva I. V., Rudoy B. A., Pirogov A. V., Tolmacheva N. G. Validation of hplc procedure for determination of gossypol in the substance Kagocel. Pharmacy, 2016, vol. 65, no. 8, pp. 18–24 (in Russian)..

11. Kasimova D. B., Gaibnozarova D. T. Validation of the method for the quantitative determination of azithromycin in the substance by HPLC. Yuzhno-ural''skie nauchnye chteniya [South Ural Scientific Readings], 2016, no. 1, pp. 59–62. (in Russian).


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ISSN 1561-8331 (Print)
ISSN 2524-2342 (Online)