Direct resolution and quantitative analysis of flurbiprofen enantiomers using microcrystalline cellulose triacetate plates: applications to the enantiomeric purity control and optical isomer determination in widely consumed drugs

• Published in: Biomedical chromatography Vol. 28; no. 1; pp. 127 - 134
• Main Authors: Del Bubba, M., Checchini, L., Ciofi, L., Furlanetto, S., Lepri, L.
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01.01.2014
• Subjects: Cellulose - chemistry; Chromatography, Thin Layer - instrumentation; Chromatography, Thin Layer - methods; Flurbiprofen - chemistry; flurbiprofen enantiomers; microcrystalline cellulose triacetate; non-commercial plates; Pharmaceutical Preparations - chemistry; quantitative determination; Stereoisomerism; thin-layer chromatography; non-commercial plates; microcrystalline cellulose triacetate; flurbiprofen enantiomers; quantitative determination; thin-layer chromatography
• ISSN: 0269-3879; 1099-0801
• DOI: 10.1002/bmc.2972

ABSTRACT Flurbiprofen enantiomers have very different pharmacological properties, since the (S)‐(+) form has a much higher anti‐inflammatory activity than the (R)‐(−) isomer, the latter being responsible for very undesirable side effects, such as gastrointestinal irritation. Based on the different biological properties of flurbiprofen enantiomers, the development of chiral chromatographic methods for the control of the enantiomeric purity is a very important topic. In this study the separation of flurbiprofen enantiomers was achieved using for the first time noncommercial MCTA layers with polyvinyl alcohol as binder, which gives to these plates a mechanical stability equivalent to that of marketed ones. Baseline resolution (α = 1.31; RS = 2.0) was obtained with ethanol–acetic acid solution (pH 3.0 ± 0.1; 60:40, v/v) as eluent and a migration distance of about 14.5 cm. Under these experimental conditions, the thin‐layer chromatography determination of the enantiomeric purity of the pharmacologically active (S)‐(+)‐flurbiprofen in the presence of 1% of the undesired (R)‐(−) form was demonstrated. Moreover, the quantitative analysis of flurbiprofen enantiomers was achieved, obtaining quantification limits and detection limits of 50 and 25 ng of each enantiomer applied to the plate, respectively. The method was succesfully applied to the enantiomer determination in widely consumed drugs, obtaining results consistent with the flurbiprofen content declared in the drug facts. Copyright © 2013 John Wiley & Sons, Ltd.