2004
VALIDATION OF A CAPILLARY ZONE ELECTROPHORESIS METHOD FOR DETERMINATION OF RIMANTADINE HYDROCHLORIDE IN RIMANTADIN100 TABLETS AND THE METHOD APPLICATION TO DISSOLUTION TEST MONITORING
PAZOUREK, Jiří; Alma REVILLA; Dagmar GAJDOŠOVÁ a Josef HAVELZákladní údaje
Originální název
VALIDATION OF A CAPILLARY ZONE ELECTROPHORESIS METHOD FOR DETERMINATION OF RIMANTADINE HYDROCHLORIDE IN RIMANTADIN100 TABLETS AND THE METHOD APPLICATION TO DISSOLUTION TEST MONITORING
Název česky
VALIDACE METODY KAPILARNI ZONOVE ELEKTROFOREZY PRO STANOVENI RIMANTADIN HYDROCHLORIDU V TABLETACH RIMANTADIN100 A APLIKACE METODY NA DISOLUCNI TESTYN TEST MONITORING
Autoři
PAZOUREK, Jiří; Alma REVILLA; Dagmar GAJDOŠOVÁ a Josef HAVEL
Vydání
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, Dekker, 2004, 0363-9045
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10406 Analytical chemistry
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 0.917
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/04:00010941
Organizační jednotka
Přírodovědecká fakulta
UT WoS
Klíčová slova anglicky
capillary zone electrophoresis
Změněno: 18. 5. 2005 13:32, doc. RNDr. Bc. Jiří Pazourek, Ph.D.
V originále
A capillary zone electrophoretic method with indirect UV-detection for determination of rimantadine, an antiviral drug against influenza A, in tablets was validated. Instrumental precision, the method precision, accuracy, calibration curve linearity, selectivity, robustness and time stability of the sample and the standard were tested. The method was also applied to monitor dissolution tests of the tablets. The possibility of internal standard for improvement of method precision was discussed.
Česky
A capillary zone electrophoretic method with indirect UV-detection for determination of rimantadine, an antiviral drug against influenza A, in tablets was validated. Instrumental precision, the method precision, accuracy, calibration curve linearity, selectivity, robustness and time stability of the sample and the standard were tested. The method was also applied to monitor dissolution tests of the tablets. The possibility of internal standard for improvement of method precision was discussed.
Návaznosti
| MSM 143100011, záměr |
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