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Extraction and Conversion Studies of the Antiaddictive Alkaloids Coronaridine, Ibogamine, Voacangine, and Ibogaine from Two Mexican Tabernaemontana Species (Apocynaceae).

Felix Krengel, Marco V Mijangos, Marisol Reyes-Lezama, Ricardo Reyes-Chilpa

Chemistry & biodiversity July 1, 2019 DOI: 10.1002/cbdv.201900175 via PubMed

Summary

AI-generated from the abstract

Methanol effectively extracts the antiaddictive alkaloids coronaridine, ibogamine, voacangine, and ibogaine (the CIVI-complex) from the root barks of Mexican Tabernaemontana alba and Tabernaemontana arborea. A one-step demethoxycarbonylation process then converts coronaridine and voacangine directly into ibogamine and ibogaine, simplifying the mixture from four to two major compounds. This protocol improves qualitative and quantitative analysis and offers a viable method for bulk production of these therapeutically important substances from these promising plant sources.

Study at a glance

Characteristics Experimental study Qualitative Peer reviewed
Population Root barks of Tabernaemontana alba and Tabernaemontana arborea
Interventions acetone ethyl acetate dichloromethane chloroform
Topics Ibogaine
Keywords Tabernaemontana apocynaceae Alkaloids Phytochemistry: detailed phytochemistry Convert
Citations 17
Key finding Methanol is the most suitable solvent for extracting the CIVI-complex from Mexican Tabernaemontana species, and a one-step demethoxycarbonylation process converts coronaridine and voacangine into ibogamine and ibogaine, simplifying analysis and enabling bulk production.

Abstract

Several species from the Apocynaceae family, such as Tabernanthe iboga, Voacanga africana, and many Tabernaemontana species, produce ibogan type alkaloids, some of which present antiaddictive properties. In this study, we used gas chromatography/mass spectrometry (GC/MS) to examine the efficiency of methanol, acetone, ethyl acetate, dichloromethane, chloroform, and hydrochloric acid in extracting the antiaddictive compounds coronaridine, ibogamine, voacangine, and ibogaine (altogether the CIVI-complex) from the root barks of Tabernaemontana alba and Tabernaemontana arborea. These Mexican species have recently shown great potential as alternative natural sources of the aforementioned substances. Methanol proved to be the most suitable solvent. Furthermore, the crude methanolic extracts could be engaged in a one-step demethoxycarbonylation process that converted coronaridine and voacangine directly into its non-carboxylic counterparts ibogamine and ibogaine, respectively, without the intermediacy of their carboxylic acids. The established protocol straightforwardly simplifies the alkaloid mixture from four to two majority compounds. In summary, our findings facilitate and improve both the qualitative and quantitative analysis of CIVI-complex-containing plant material, as well as outlining a viable method for the bulk production of these scientifically and pharmaceutically important substances from Mexican Tabernaemontana species.

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