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Resolution and determination of enantiomeric purity of the enantiomers of felodipine using chiral‐AGP® as stationary phase
Author(s) -
Karlsson Anders,
Pettersson Karin,
Hernqvist Kerstin
Publication year - 1995
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.530070307
Subject(s) - chemistry , felodipine , enantiomer , racemization , resolution (logic) , chromatography , phase (matter) , detection limit , organic chemistry , medicine , artificial intelligence , computer science , blood pressure , radiology
A direct chiral chromatographic reversed phase method for the determination of the enantiomers of felodipine is described. The influence of charged and uncharged modifiers as well as the effect of the mobile phase pH on the enantiomeric resolution is discussed. A high mobile phase pH and the addition of 2‐propanol as organic modifier gave the highest separation factor (α = 1.3). The high mobile phase pH (pH = 7.6) is outside the recommended pH limit of silica based columns but was necessary to achieve baseline resolution of (R)‐ and (S)‐felodipine. Improvement of column efficiency by increasing column temperature was utilized for optimization of the enantiomeric resolution (Rs = 1.7). The enantiomers of felodipine and three related compounds were separated within 15 min. The enantiomeric purity of (R)‐ and (S)‐felodipine in injections and (R)‐felodipine in bulk substance was higher than 99.5% and no racemization was observed after storage at accelerated conditions. A poor Chiral‐AGP® column used for a long period was restored using a simple wash step together with repacking the top of the chromatographic column. © 1995 Wiley‐Liss, Inc.