# Electrospray–Mass Spectrometry-Guided Targeted Isolation of Indole Alkaloids from Leaves of Catharanthus roseus by Using High-Performance Countercurrent Chromatography

**Authors:** Mahdi Yahyazadeh, Dirk Selmar, Gerold Jerz

PMC · DOI: 10.3390/molecules30102115 · 2025-05-09

## TL;DR

Scientists isolated six major indole alkaloids from Catharanthus roseus leaves using a mass spectrometry-guided chromatography method.

## Contribution

A novel electrospray-mass spectrometry guided HPCCC method was developed for targeted isolation of indole alkaloids.

## Key findings

- Six indole alkaloids were successfully isolated and identified using NMR spectroscopy.
- The biphasic solvent system with trifluoroacetic acid improved separation efficiency.
- Electrospray mass spectrometry enabled real-time monitoring of metabolite recovery.

## Abstract

Electrospray mass spectrometry off-line profiling monitored the recovery of targeted indole alkaloids from a fortified crude extract of Catharanthus roseus (790 mg) using semi-preparative high-performance countercurrent chromatography (HPCCC) fractionation. Visualization of selected single-ion traces projected the HPCCC molecular weight elution profile. Experimental partition-ratio values KD and peak widths for detected metabolites were determined. Structural characterization of metabolites and co-elution effects were monitored in the scan range m/z 100–2000. In this study, the biphasic solvent system containing n-hexane–n-butanol–water with 0.5% ion-pair reagent trifluoro-acetic acid [1:1:2, v/v/v] was used based on partition ratio KD-value liquid chromatography–electrospray ionization–mass spectrometry (LC-ESI-MS) analysis prediction. The monitoring of target ions resulted in the isolation of six major concentrated indole alkaloids (akuammicine, catharanthine, perivine, vindoline, vindorosine, and 19R-vindolinine), which were fully elucidated by 1D and 2D nuclear magnetic resonance (NMR) spectroscopy.

## Linked entities

- **Chemicals:** trifluoro-acetic acid (PubChem CID 6422), akuammicine (PubChem CID 10314057), catharanthine (PubChem CID 197771), perivine (PubChem CID 6473766), vindoline (PubChem CID 260535), vindorosine (PubChem CID 261578)
- **Species:** Catharanthus roseus (taxon 4058)

## Full-text entities

- **Chemicals:** hexane (MESH:D006586), trifluoro-acetic acid (MESH:D014269), Indole Alkaloids (MESH:D026121), butanol (MESH:D000440), catharanthine (MESH:C017836), vindoline (MESH:C009667), water (MESH:D014867), 19R (-), vindolinine (MESH:C009668), vindorosine (MESH:C514721), akuammicine (MESH:C434103)
- **Species:** Catharanthus roseus (chatas, species) [taxon 4058]

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12113773/full.md

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Source: https://tomesphere.com/paper/PMC12113773