Preview

Regulatory Research and Medicine Evaluation

Advanced search

Basic requirements for biological criteria in drug quality evaluation. validation of biological control methods

Abstract

Drug quality evaluation and control involve extensive use of biological methods in addition to chemical, physico-chemical and microbiological ones in order to ensure drug identity, purity and safety. Basic requirements for biological testing criteria are stated in the State Pharmacopoeia of the Russian Federation, however some aspects of testing are not described in sufficient detail and depend on the nature of a medicine to be tested. The present article describes basic requirements for introducing «Bacterial endotoxins» and «Abnormal toxicity» parameters to normative documentation. It also outlines basic aspects of test conditions validation and determination of an adequate level of drug quality standards.

About the Authors

N. P. Neugodova
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


M. S. Ryabtseva
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


G. A. Sapozhnikova
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


References

1. Severtsev VA, Mashkovskiy MD, Bagirova VL, et al. Guidelines for the introduction of the section «pyrogen test» in the technical documentation for the newly developed injectable drugs, as well as water and other fluids used in their manufacture, and articles, which touch or that contain solutions for injection. Guidelines. Moscow; 1990 (in Russian).

2. Yurgel NV, Kosenko VV, Davydova KS, Budanov SV, Bagirova VL, Kovaleva EL, et al. Rules of compilation, presentation and design quality standards for pharmaceutical substances. Guidelines. Moscow; 2009 (in Russian).

3. State register of medicines. V. II, parts 1 and 2. Moscow: Official publication; 2009 (in Russian).

4. Shapovalova OV, Dolgova GV, Neugodova NP. Features of the development of section «Bacterial endotoxins» for antibiotic substances. Antibiotiki i himioterapiya 2008; 53(11–12): 34–58 (in Russian).

5. Shapovalova OV, Dolgova GV, Neugodova NP, Sapozhnikova GA. Methodological approaches to the elaboration of «Bacterial endotoxins » index in the pharmaceutical substances. Vedomosti Nauchnogo tsentra ekspertizy sredstv meditsinskogo primeneniya

6. 2012; (2): 47–50 (in Russian).

7. Shapovalova OV, Dolgova GV, Neugodova NP, Sapozhnikova GA. The use of organic solvents to determine of «Bacterial endotoxins» index in the water-insoluble pharmaceutical substances. Antibiotiki i himioterapiya 2013; (9): 41–4 (in Russian).

8. Merkulova YuV, Dolgova GV, Neugodova NP, Chayka LA, Gomon ON, Shapovalova OV. Properties of the test to bacterial endotoxins of medicines in the form of oily solutions. Farmakom 2008; (1): 67–73 (in Russian).

9. Pershin GN. Methods of experimental chemotherapy. Moscow: Meditsina; 1971 (in Russian).

10. Krylov YuF, Kivman GYa. Biological control of drug safety. Moscow: Meditsina; 1985 (in Russian).

11. Neugodova NP, Dolgova GV, Hayretdinova MN, Pomerantseva TYa, Sapozhnikova GA, Verstakova OL. The procedure of the implementation of pharmaceutical index «Abnormal Toxicity» by the example of antibiotics. Antibiotiki i himioterapiya 2008; 53(7–8): 19–26 (in Russian).

12. Neugodova NP, Dolgova GV, Sapozhnikova GA, Lutseva AI. Approaches to the assessment of biosimilars safety. Vedomosti Nauchnogo tsentra ekspertizy sredstv meditsinskogo primeneniya 2013; (3): 32–4 (in Russian).

13. Sharoykina MV, Kovaleva EL, Neugodova NP. Methodical approaches to the estimation of abnormal toxicity cephalosporin antibiotics. Sechenovskiy vestnik 2014; 16(2): 111 (in Russian).

14. Neugodova NP, Dolgova GV, Pomerantseva TYa, Hayretdinova MN, Sapozhnikova GA. Effect of parameter «Injection rate» during the test «The test for toxicity». Antibiotiki i himioterapiya 2009; (1): 53–5 (in Russian).

15. Sharoykina MV, Ryabtseva MS, Kovaleva EL, Neugodova NP. Effect of parameter «Injection rate» during the test «Abnormal Toxicity» to ensure the quality of the antibiotic cephalosporin group—ceftriaxone. Antibiotiki i himioterapiya 2015; (1–2): 35–8 (in Russian).

16. Karkischenko NN, Grachev SV. Guide to laboratory animals and alternative models in biomedical research. Moscow: Profile–2C; 2010 (in Russian).

17. The Triptofan Incident. European Federation of Biotechnology. Fact Sheet 1. Available from: http://www.quackwatch.com/01Quackery-RelatedTopics/DSH/trypto.html.

18. U. S. Food and Drug Administration. Available from: http://www.fda.gov/default.htm.

19. Garbe YHO, Osborne C, Beggs K, Bopst M, Jos A, Kitashova AA, et al. Exclusion of test for abnormal toxicity as a quality control test: a historical analysis of the data and scientific knowledge. Razrabotka i registratsiya lekarstvennyh sredstv 2015; 2(11): 184–92 (in Russian).

20. Karkischenko NN. Alternatives of biomedicine. Moscow: Mezhakademicheskoe izdatelstvo VPK; 2010 (in Russian).


Review

For citations:


Neugodova N.P., Ryabtseva M.S., Sapozhnikova G.A. Basic requirements for biological criteria in drug quality evaluation. validation of biological control methods. The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products. 2016;(3):3-8. (In Russ.)

Views: 2446


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 3034-3062 (Print)
ISSN 3034-3453 (Online)