Validation of an ultra-fast UPLC-UV method for the separation of antituberculosis tablets

Journal of Separation Science

Volumn 31, Issue 6-7, 2008, Pages 1050-1056

  Nguyen, Dao T T ^a,b   Guillarme, Davy ^a,b   Rudaz, Serge ^a,b   Veuthey, Jean Luc ^a,b  

^a UNIVERSITY OF GENEVA   (Switzerland)

^b UNIVERSITY OF LAUSANNE   (Switzerland)

Author keywords

Antituberculosis; Fast LC; High temperature; HT UPLC; Method validation

Indexed keywords

DRUG DOSAGE; DRUG PRODUCTS; FLOW RATE; HIGH TEMPERATURE EFFECTS;

ANTITUBERCULOSIS DRUGS; ANTITUBERCULOSIS TABLETS; DOSAGE FORM; METHOD VALIDATION;

LIQUID CHROMATOGRAPHY;

ISONIAZID; PYRAZINAMIDE; RIFAMPICIN; RIFATER; TUBERCULOSTATIC AGENT;

ACCURACY; ARTICLE; CONTROLLED STUDY; DRUG DETERMINATION; DRUG MIXTURE; DRUG STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIGH TEMPERATURE PROCEDURES; INTERMETHOD COMPARISON; PRIORITY JOURNAL; QUALITY CONTROL; REPRODUCIBILITY; RESPONSE TIME; TABLET FORMULATION; TEMPERATURE SENSITIVITY; ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY; ULTRAVIOLET RADIATION; VALIDATION PROCESS;

ANTITUBERCULAR AGENTS; CHROMATOGRAPHY, LIQUID; MOLECULAR STRUCTURE; REPRODUCIBILITY OF RESULTS; TABLETS; TEMPERATURE; TIME FACTORS;

EID: 43249115914     PISSN: 16159306     EISSN: 16159314     Source Type: Journal    
DOI: 10.1002/jssc.200700537     Document Type: Article

References (24)

1. U.S. Pharmacopeia 28-NF23,2005, pp. 1731-1732.
2. Mazzeo, J. R., Neue, U. D., Kele, M., Plumb, R. S., Anal. Chem. 2005, 77, 460A-467A.
3. Swartz, M. E., LCGC North Am. 2005, Suppl., 8-14.
4. Novakova, L., Matysova, L., Solich, P., Talanta 2006, 68, 908-918.
5. Nguyen, D. T. T., Guillarme, D., Rudaz, S., Veuthey, J. L., J. Sep. Sci. 2006, 29, 1836-1848.
6. Nguyen, D. T. T., Guillarme, D., Rudaz, S., Veuthey, J. L., J. Chromatogr. A 2006, 1128, 105-113.
7. Guìllarme, D., Nguyen, D. T. T., Rudaz, S., Veuthey, J. L., Eur. J. Pharm. Biopharm. 2007, 66, 475-482.
8. Guìllarme, D., Nguyen, D. T. T., Rudaz, S., Veuthey, J. L., Eur. J. Pharm. Biopharm. 2008, 68, 30-440.
9. Yan, B., Zhao, J., Brown, J. S., Blackwell, J., Carr, P. W., Anal. Chem. 2000, 72, 1253-1262.
10. Clark, J., Pharm. Technol. Europe 2004, 16, 41-42, 45.
11. Dolan, J. W., J. Chromatogr. A 2002, 965, 195-205.
12. Yang, X., Ma, L., Carr, P. W., J. Chromatogr. A 2005, 1079, 213-220.
13. Barrioulet, M. P., Heinisch, S., Rocca, J. L., Spectra Anal. 2007, 36, 38-44.
14. Guillarme, D., Heinisch, S., Rocca, J. L., J. Chromatogr. A 2004, 1052, 39-51.
15. Guillarme, D., Russo, R., Rudaz, S., Bicchi, C., Veuthey, J. L., Curr. Pharm. Anal. 2007, 4, 221-229.
16. Nguyen, D. T. T., Guillarme, D., Heinisch, S., Barrioulet, M. P., Rocca, J. L., Rudaz, S., Veuthey, J. L., J. Chromatogr. A 2007, 1167, 76-84.
17. Hubert, P., Nguyen-Hu, J. J., Boulanger, B., Chapuzet, E., Chiap, P., Cohen, N., Compagnon, P. A., Dewe, W,, Feinberg, M., Lallier, M., Laurentie, M., Mercier, N., Muzard, G., Nivet, C., Valat, L., STP Pharma Pratiques 2003, 13, 101-138.
18. International conference on harmonization (ICH) of technical requirements for registration of pharmaceuticals for human use, topic Q2 (R1): Validation of analytical procedures: Text and methodology, Geneva, 2005.
19. Hubert, P., Chiap, P., Crommen, J., Boulanger, B., Chapuzet, E., Mercier, N., Bervoas-Martin, S., Chevalier, P., Grandjean, D., Lagorce, P., Lallier, M., Laparra, M. C., Laurentie, M., Nivet, J. C., Anal. Chim. Acta 1999, 391, 135-148.
20. Boulanger, B., Chiap, P., Dewe, W., Crommen, J., Hubert, P., J. Pharm. Biomed. Anal. 2003, 32, 753-765.
21. Mohan, B., Sharda, N., Singh, S., J. Pharm. Biomed. Anal. 2003, 31, 607-612.
22. Heinisch, S., Puy, G., Barrioulet, M. P., Rocca, J. L., J. Chromatogr. A 2006, 1118, 234-243.
23. Cuadros-Rodriguez, L., Bagur-Gonzalez, M. G., Sanchez-Vinas, M., Gonzalez-Casado, A., Gomez-Saez, A. M., J. Chromatogr. A 2007, 1158, 33-46.
24. Thompson, J. D., Carr, P. W., Anal. Chem. 2002, 74, 1017-1023.