A validated chiral LC method for the enantiomeric separation of Zolmitriptan key intermediate, ZTR-5
A new and accurate chiral liquid chromatographic method was described for the enantiomeric separation of ZTR-5 [(4 S)-4-(4-aminobenzyl)-2-oxazolidinone, ( S)-isomer], a key intermediate of Zolmitriptan in bulk drugs. The enantiomers of ZTR-5 were baseline resolved on a Chiralpak AD-H (250 mm × 4.6 m...
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Veröffentlicht in: | Journal of pharmaceutical and biomedical analysis 2005-09, Vol.39 (3), p.796-800 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A new and accurate chiral liquid chromatographic method was described for the enantiomeric separation of ZTR-5 [(4
S)-4-(4-aminobenzyl)-2-oxazolidinone, (
S)-isomer], a key intermediate of Zolmitriptan in bulk drugs. The enantiomers of ZTR-5 were baseline resolved on a Chiralpak AD-H (250
mm
×
4.6
mm, 5
μm) column using a mobile phase system containing hexane:ethanol (70:30, v/v). The resolution between the enantiomers was not less than four and interestingly distomer was eluted prior to eutomer. The limit of detection and limit of quantification of (4
R)-4-(4-aminobenzyl)-2-oxazolidinone [(
R)-isomer] were found to be 250 and 750
ng/ml, respectively, for 10
μl injection volume. The percentage recovery of (
R)-isomer ranged from 92.0 to 105.6 in the bulk drug samples of ZTR-5. The validated method yielded good results regarding precision, linearity, accuracy and ruggedness. The proposed method was found to be suitable and accurate for the quantitative determination of (
R)-isomer in bulk drug samples of ZTR-5. |
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ISSN: | 0731-7085 1873-264X |
DOI: | 10.1016/j.jpba.2005.04.043 |