Enantiomeric separation of proton pump inhibitors on new generation chiral columns using LC and supercritical fluid chromatography

被引:26
作者
Chennuru, Lakshmi Narayana [1 ]
Choppari, Thirupathi [1 ]
Duvvuri, Subrahmanyam [2 ]
Dubey, Pramod Kumar [3 ]
机构
[1] Daicel Chiral Technol India Pvt Ltd, Hyderabad 500078, Andhra Pradesh, India
[2] Rat Labs Pvt Ltd, Hyderabad, Andhra Pradesh, India
[3] JNT Univ, Dept Chem, Hyderabad, Andhra Pradesh, India
关键词
CHIRALPAK IC; Enantioselectivity; Laser polarimetry; Proton pump inhibitors; Supercritical fluid chromatography; PERFORMANCE LIQUID-CHROMATOGRAPHY; STATIONARY-PHASE; ENANTIOSELECTIVE DISPOSITION; CYP2C19; GENOTYPES; PHARMACOKINETIC DIFFERENCES; LANSOPRAZOLE ENANTIOMERS; OMEPRAZOLE; RESOLUTION; DRUGS; 3,5-DIMETHYLPHENYLCARBAMATE;
D O I
10.1002/jssc.201300419
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The enantioselectivity of proton pump inhibitors, namely, omeprazole, lansoprazole, rabeprazole, pantoprazole, tenatoprazole, and ilaprazole were studied using new generation chiral packing materials: CHIRALPAK IA, CHIRALPAK IB, and CHIRALPAK IC. Two versatile techniques, HPLC and supercritical fluid chromatography (SFC) were used in this study. CHIRALPAK IC has shown superior selectivity under both LC and SFC conditions, whereas CHIRALPAK IA has shown good selectivity in SFC when compared to LC under primary screening conditions. The chiral recognition ability in LC and SFC modes were found to be in the order CHIRALPAK IC > CHIRALPAK IA > CHIRALPAK IB. In addition to diode array detection, chiral detection was carried out using a laser polarimeter and the elution orders were found to be the same in both LC and SFC elution modes. Mobile phase modifiers and column temperature effects were also studied. In SFC, modifiers (co-solvent) elution strength was found to be in the order ethanol > methanol > 2-propanol > acetonitrile. In both LC and SFC, a decrease in retention and increase in resolution with an increase in temperature was noticed for all the proton pump inhibitors.
引用
收藏
页码:3004 / 3010
页数:7
相关论文
共 39 条
[1]   Putting chirality to work: The strategy of chiral switches [J].
Agranat, I ;
Caner, H ;
Caldwell, A .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (10) :753-768
[2]   Intellectual property and chirality of drugs [J].
Agranat, I ;
Caner, H .
DRUG DISCOVERY TODAY, 1999, 4 (07) :313-321
[3]   DIRECT OPTICAL RESOLUTION OF A SERIES OF PHARMACOLOGICALLY ACTIVE RACEMIC SULFOXIDES BY HIGH-PERFORMANCE LIQUID AFFINITY-CHROMATOGRAPHY [J].
ALLENMARK, S ;
BOMGREN, B ;
BOREN, H ;
LAGERSTROM, PO .
ANALYTICAL BIOCHEMISTRY, 1984, 136 (02) :293-297
[4]   Single-isomer drugs - True therapeutic advances [J].
Andersson, T .
CLINICAL PHARMACOKINETICS, 2004, 43 (05) :279-285
[5]   Pharmacokinetic studies with esomeprazole, the (S)-isomer of omeprazole [J].
Andersson, T ;
Hassan-Alin, M ;
Hasselgren, G ;
Röhss, K ;
Weidolf, L .
CLINICAL PHARMACOKINETICS, 2001, 40 (06) :411-426
[6]   STEREOSELECTIVE EFFECTS IN THE SEPARATION OF ENANTIOMERS OF OMEPRAZOLE AND OTHER SUBSTITUTED BENZIMIDAZOLES ON DIFFERENT CHIRAL STATIONARY PHASES [J].
BALMER, K ;
PERSSON, BA ;
LAGERSTROM, PO .
JOURNAL OF CHROMATOGRAPHY A, 1994, 660 (1-2) :269-273
[7]   LANSOPRAZOLE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND ITS THERAPEUTIC EFFICACY IN ACID-RELATED DISORDERS [J].
BARRADELL, LB ;
FAULDS, D ;
MCTAVISH, D .
DRUGS, 1992, 44 (02) :225-250
[8]  
BERGER T, 1995, PACKED COLUMN SUPERC
[9]   Pharmaceutical analysis by supercritical fluid chromatography: Optimization of the mobile phase composition on a 2-ethylpyridine column [J].
Brunellil, Claudio ;
Zha, Yining ;
Brown, Melissa-Hanna ;
Sandra, Pat .
JOURNAL OF SEPARATION SCIENCE, 2008, 31 (08) :1299-1306
[10]   High-performance liquid chromatography enantioseparation of proton pump inhibitors using the immobilized amylose-based Chiralpak IA chiral stationary phase in normal-phase, polar organic and reversed-phase conditions [J].
Cirilli, Roberto ;
Ferretti, Rosella ;
Gallinella, Bruno ;
De Santis, Emiliana ;
Zanitti, Leo ;
La Torre, Francesco .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1177 (01) :105-113