1. Academic Validation
  2. Online acetylcholinesterase inhibition evaluation by high-performance liquid chromatography-mass spectrometry hyphenated with an immobilized enzyme reactor

Online acetylcholinesterase inhibition evaluation by high-performance liquid chromatography-mass spectrometry hyphenated with an immobilized enzyme reactor

  • J Chromatogr A. 2020 Jan 4;1609:460506. doi: 10.1016/j.chroma.2019.460506.
Ye Yuan 1 Minjie Zhao 1 Ludivine Riffault-Valois 1 Saïd Ennahar 1 Martine Bergaentzlé 1 Eric Marchioni 2
Affiliations

Affiliations

  • 1 IPHC, UNISTRA, CNRS, Faculté de pharmacie, 74, route du Rhin, 67400 Illkirch, France.
  • 2 IPHC, UNISTRA, CNRS, Faculté de pharmacie, 74, route du Rhin, 67400 Illkirch, France. Electronic address: eric.marchioni@unistra.fr.
Abstract

A high-performance liquid chromatography-mass spectrometry technique hyphenated on-line with an immobilized Enzyme reactor (IMER) was developed by the use of 3 known acetylcholinesterase (AChE) inhibitors (galanthamine, huperzine A and tacrine). This bioanalytical device allows qualitative comparison of the inhibitory strengths of AChE inhibitors. The AChE inhibitory strengths were evaluated and compared by the corresponding acetylcholine peak areas (mass signal) obtained after a chromatographic separation and the elution through the IMER. Only one injection of the analytes is needed to get this comparative analysis. This bioanalytical device was then applied to the extract of a natural plant, Lycoris radiata, which is known to contain AChE inhibitors such as galanthamine and lycoramine. Aside from the demonstration of the inhibitory activity of the two known AChE inhibitors, the AChE inhibitory activity of another compound (dihydro-latifaliumin C) was revealed. This is the first report describing the AChE inhibitory activity of this compound.

Keywords

Acetylcholinesterase inhibitor; Alkaloid; Bioanalytical device; Immobilized enzyme reactor; MS.

Figures
Products