ArticleJournal of liquid chromatography & related technologies2017
Determination of the enantiomeric purity of epinephrine by HPLC with circular dichroism detection.
Article in Journal of liquid chromatography & related technologies, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 33 citations in OpenAlex.
- Glycine-Copper Nanozyme with Dual Oxidase Activity: for Colorimetric Detection of Epinephrine and Oxidation of Phenolic Pollutants.ACS omega · 2026Article
- Latest developments in the detection and quantification of adrenaline: advances and clinical applications.Bioanalysis · 2025Review
- Review
- Screen-printed disposable electrodes using graphite-polyurethane composites modified with magnetite and chitosan-coated magnetite nanoparticles for voltammetric epinephrine sensing: a comparative study.Mikrochimica acta · 2020Article
- Fluorescence Sensing Platforms for Epinephrine Detection Based on Low Temperature Cofired Ceramics.Sensors (Basel, Switzerland) · 2020Article
- Enantiomeric impurity analysis using circular dichroism spectroscopy with United States Pharmacopeia liquid chromatographic methods.Journal of pharmaceutical and biomedical analysis · 2018Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
Several hundred drug substances approved by the U.S. Food and Drug Administration are chiral molecules. For the enantiomeric purity assessment, current practice is to develop separation techniques using chiral columns or mobile phase modifiers to separate enantiomers before detection. An alternative approach is to use currently accepted HPLC assay methods and use chiral-specific detectors to confirm whether the correct enantiomer is present. In this paper, adding a circular dichroism (CD) detector to an achiral HPLC method from the US Pharmacopeia (USP) is shown to be amenable for the determination of the enantiomeric purity of epinephrine, a substance used to treat anaphylaxis. This HPLC-UV-CD approach was able to detect the inactive D-(+) enantiomer at 1% of the total epinephrine composition. The linearity, accuracy, and precision of HPLC-UV-CD were evaluated and compared to analyses using a chiral HPLC method. Additionally, an epinephrine drug product was analyzed for assay (concentration) and enantiomeric purity. The results from achiral and chiral methods were identical within the experimental error. Overall, achiral chromatography performed using a USP method with CD detection may serve as a general means of determining chiral drug enantiomer purity and avoids the need for the development of additional chiral-specific methods for each individual drug.
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Registered trials
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