Bioequivalence evaluation of two omeprazole enteric-coated formulations in humans

被引:25
作者
Farinha, A [1 ]
Bica, A [1 ]
Pais, JP [1 ]
Toscano, MC [1 ]
Tavares, P [1 ]
机构
[1] Lab Estudos Farmaceut, P-1400 Lisbon, Portugal
关键词
omeprazole; bioequivalence; enteric-coating; presentation of results; liquid chromatography;
D O I
10.1016/S0928-0987(98)00043-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Omeprazole, a proton pump inhibitor, effectively suppresses the gastric acid secretion in the parietal cells of the stomach. Several previously published papers focus on the pharmacokinetics of the drug and its interactions with physiological aspects or with other drugs. The increasing number of omeprazole containing products available in the market, raises questions of therapeutic equivalence and/or generic substitution. The bioequivalence evaluation between two or more formulations provides information about in vivo performance. In a favorable decision regarding bioequivalence, the products are considered to have a similar therapeutic efficacy when used under the same therapeutic conditions. This paper reports the design, results and some important aspects involved in a bioequivalence study between two solid oral formulations from different manufacturers. Some important findings were the high intra-suject variability observed for C-max and the variability observed between subject profiles, probably caused by the multi-unit type of formulations studied. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:311 / 315
页数:5
相关论文
共 11 条
[1]   ORAL BIOAVAILABILITY OF OMEPRAZOLE BEFORE AND AFTER CHRONIC THERAPY IN PATIENTS WITH DUODENAL-ULCER [J].
CHING, MS ;
MIHALY, GW ;
ANGUS, PW ;
MORGAN, DJ ;
DEVENISHMEARES, S ;
YEOMANS, ND ;
SMALLWOOD, RA .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1991, 31 (02) :166-170
[2]  
*CPMP, 1992, WORK PART EFF MED PR
[3]  
*FDA, 1992, 1090BA CFR FDA
[4]  
HAUSCHKE D, 1992, INT J CLIN PHARM TH, V28, P105
[5]   ORAL PHARMACOKINETICS OF OMEPRAZOLE [J].
HOWDEN, CW ;
MEREDITH, PA ;
FORREST, JAH ;
REID, JL .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1984, 26 (05) :641-643
[6]   CLINICAL-PHARMACOLOGY OF OMEPRAZOLE [J].
HOWDEN, CW .
CLINICAL PHARMACOKINETICS, 1991, 20 (01) :38-49
[7]   SIMULTANEOUS DETERMINATION OF OMEPRAZOLE AND ITS METABOLITES IN PLASMA AND URINE BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH AN ALKALINE-RESISTANT POLYMER-COATED C18 COLUMN [J].
KOBAYASHI, K ;
CHIBA, K ;
SOHN, DR ;
KATO, Y ;
ISHIZAKI, T .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1992, 579 (02) :299-305
[8]   STABILITY OF OMEPRAZOLE SOLUTIONS AT VARIOUS PH VALUES AS DETERMINED BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
MATHEW, M ;
DASGUPTA, V ;
BAILEY, RE .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1995, 21 (08) :965-971
[9]   A COMPARISON OF THE 2 ONE-SIDED TESTS PROCEDURE AND THE POWER APPROACH FOR ASSESSING THE EQUIVALENCE OF AVERAGE BIOAVAILABILITY [J].
SCHUIRMANN, DJ .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1987, 15 (06) :657-680
[10]  
STEINIJANS VW, 1995, INT J CLIN PHARM TH, V33, P427