Planta Med 2004; 70(8): 764-770
DOI: 10.1055/s-2004-827209
Original Paper
Analytical Methods
© Georg Thieme Verlag KG Stuttgart · New York

Development and Validation of a High Performance Liquid Chromatographic Method for Quantitative Determination of Aporphine Alkaloids from Different Samples of Cassytha filiformis

Caroline Stévigny1 , Marie-Caroline Wautier1 , Jean-Louis Habib Jiwan2 , Patrice Chiap3 , Philippe Hubert3 , Joëlle Quetin-Leclercq1
  • 1Laboratoire de Pharmacognosie, Unité d’Analyse Chimique et Physico-Chimique des Médicaments, Université Catholique de Louvain, UCL 72.30-CHAM, Bruxelles, Belgium
  • 2Laboratoire de Spectrométrie de Masse, Université Catholique de Louvain, Faculté des Sciences, Département de Chimie, Louvain-la-Neuve, Belgium
  • 3Laboratoire d’Analyse des Médicaments, Université de Liège, Département de Pharmacie, CHU, B36, Liège, Belgium
Further Information

Publication History

Received: January 22, 2004

Accepted: May 8, 2004

Publication Date:
24 August 2004 (online)

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Abstract

A sensitive and accurate procedure based on an alkaloid extraction coupled to an HPLC-UV-MS determination has been developed for the separation and quantification of the major aporphines in Cassytha filiformis. The extraction step and the liquid chromatography conditions were optimized in order to improve the selectivity of the method. The HPLC mobile phase consisted of a mixture of water containing 10 mM ammonium acetate adjusted to pH 3 with acetic acid-acetonitrile (90 : 10, v/v) (A) and acetonitrile (B) used in a gradient mode (0 to 40 %). The stationary phase was an RP-select B (5 μm) column. The method was completely validated using cassythine, one of the major aporphines in our samples, as reference standard and successfully applied to the determination of these pharmacologically interesting aporphines in seven different batches of C. filiformis. The detection and quantitation limits of cassythine were found to be 13 and 20 μg/mL, respectively. The results showed variations in the total alkaloid content in samples from 0.11 to 0.43 %.

References

Prof. J. Quetin-Leclercq

Laboratoire de Pharmacognosie

Unité CHAM

UCL 72.30

Avenue E. Mounier 72

1200 Brussels

Belgium

Fax: +32-2-764-72-53

Email: leclercq@cham.ucl.ac.be