Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5161
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dc.contributor.authorAlwera, Shiv-
dc.date.accessioned2023-08-24T09:57:26Z-
dc.date.available2023-08-24T09:57:26Z-
dc.date.issued2021-
dc.identifier.citationJPC – Journal of Planar Chromatography –Modern TLC, 34(3), 211–215.en_US
dc.identifier.urihttps://doi.org/10.1007/s00764-021-00109-5-
dc.identifier.urihttp://hdl.handle.net/123456789/5161-
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractThis work reports the enantioresolution of (RS)-acebutolol (ACB) by a thin-layer chromatographic method involving colistin sulfate (CS) as chiral selector. For this purpose, glass plates of dimension (12 cm × 4 cm × 0.4 cm) were prepared and used in four different approaches. The chiral selector was used in four different approaches before or during the chromatographic processes. Out of several mobile phase systems tried, the mobile phase system MeCN–MeOH−H2O (5.5:2.5:1.0, V/V) was found to be successful for better resolution (RS  =  2.2). To confirm the elution order, the chromatograms of (RS)-ACB were developed along with the pure enantiomer of ACB, i.e., (R)-ACB, and it was concluded that (R)-ACB eluted before (S)-enantiomer. The detection limit for each enantiomer of ACB was found in the range 12−15 μg spot−1. The developed method can be applied for the enantioresolution of ACB and its analogs in dosage formulations.en_US
dc.language.isoen_USen_US
dc.publisherSpringer Linken_US
dc.subjectthin-layeren_US
dc.subjectchromatographyen_US
dc.subjectenantioresolutionen_US
dc.subjectacebutololen_US
dc.titleDifferent approaches in thin-layer chromatography for enantioresolution of acebutolol using colistin sulfate as chiral selectoren_US
dc.typeArticleen_US
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