Planta Medica International Open 2017; 4(S 01): S1-S202
DOI: 10.1055/s-0037-1608215
Poster Session
Georg Thieme Verlag KG Stuttgart · New York

Combined determination of sennosides, monomeric hydroxyanthacene glycosides and anthraquinone aglycones by UHPLC-DAD

A Schenk
1   Department of Analytical Development, Max Zeller Söhne AG, Romanshorn, Switzerland
,
LN Ziegler
1   Department of Analytical Development, Max Zeller Söhne AG, Romanshorn, Switzerland
,
N Meier
2   Department of Life Sciences of Zurich University of Applied Sciences, Wädenswil, Switzerland
,
S Peter
2   Department of Life Sciences of Zurich University of Applied Sciences, Wädenswil, Switzerland
,
E Wolfram
2   Department of Life Sciences of Zurich University of Applied Sciences, Wädenswil, Switzerland
› Author Affiliations
Further Information

Publication History

Publication Date:
24 October 2017 (online)

 
 

    Using a coreshell column, the new UHPLC-DAD method allows almost a baseline separation of seven sennosides and the monomeric hydroxyanthracene glycosides rhein 8-glycoside and aloe emodin 8-glycoside in senna pod dry extract and in a senna-fig syrup preparation. UV and mass spectrometry studies show that none of the peaks of interest is underlaid by flavonoids, a fact which, in the case of other LC methods for sennosides, requires a sample processing by means of SPE. Sennosides are determined by sennoside B, monomeric hydroyanthracene glycosides by rhein 8-glycoside as external standard. The combined determination of all hyrdoxyanthracene glycosides is important for pharmaceutical stability testing because sennosides are partly degraded to rhein- and aloe emodin 8-glycoside. In the posterior part of the chromatogram the aglycones rhein and aloe emodine can be determined. The complete assay runs 19 min.


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