Determination of glucosamine and monitoring of its mutarotation by hydrophilic interaction liquid chromatography with evaporative light scattering detector
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
30120782
DOI
10.1002/bmc.4368
Knihovny.cz E-resources
- Keywords
- ELSD, HILIC, calibration, glucosamine, mutarotation,
- MeSH
- Chromatography, Liquid methods MeSH
- Glucosamine analysis chemistry MeSH
- Hydrophobic and Hydrophilic Interactions MeSH
- Isomerism MeSH
- Linear Models MeSH
- Scattering, Radiation * MeSH
- Reproducibility of Results MeSH
- Light MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Glucosamine MeSH
Saccharides and their derivatives are typical polar analytes without a suitable UV-chromophore that are nowadays analyzed by HPLC (high-performance liquid chromatography) under HILIC (hydrophilic interaction liquid chromatography) mode. Usually an evaporative light scattering detector (ELSD) is utilized which, however, gives a nonlinear response. A procedure to overcome the problem of mutarotating (time-varying) analytes recorded with such a nonlinear response detector is described. The procedure was applied for determination of glucosamine in two commercially available pharmaceutical formulations containing the common inorganic ions that the detector gives a response to. Under optimized conditions, both the anomers of glucosamine were separated and could be determined separately. Owing to the short retention time of the analyte (a run time <4 min) and relatively slow kinetics of the anomeric conversion (equilibration time 2.5 h), mutarotation could be monitored and corresponding rate constants calculated.
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