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Marinobufagenin extraction from Rhinella marina toad glands: alternative approaches for a systematized strategy
Lenaerts, C.; Wells, M.; Hambye, S.; Blankert, B. (2019). Marinobufagenin extraction from Rhinella marina toad glands: alternative approaches for a systematized strategy. Journal of separation science 42(7): 1384-1392. https://hdl.handle.net/10.1002/jssc.201800879
In: Journal of separation science. ISSN 1615-9306; e-ISSN 1615-9314
Peer reviewed article  

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Author keywords
    high-performance liquid chromatography; marinobufagenin; thin-layer chromatography; toad venom

Auteurs  Top 
  • Lenaerts, C.
  • Wells, M.
  • Hambÿe, S.
  • Blankert, B.

Abstract
    Marinobufagenin is a bufadienolide compound detected mainly in skin and parotoid gland secretions of Rhinella marina (L.) toad. Bufadienolides regulate the Na+/K+-ATPase pump by inhibiting the cardiotonic steroid dependent-site and act as cardiac inotropes with vasoconstrictive properties. Marinobufagenin and other bufadienolides, such as telocinobufagin and bufalin, are thought to be found endogenously in mammals in salt-sensitive hypertensive states such as essential hypertension, congestive heart-failure, and preeclampsia. The role of marinobufagenin as antimicrobial agent and its cytotoxic potential have also been recognized. The particular interest around marinobufagenin prompts us to consider the Rhinella marina toad venom as a possible source for molecules with pharmacological and/or diagnostic potential. In this article, two different approaches of extraction and purification of marinobufagenin from Rhinella marina (L.) venom are studied: (i) Preparative thin-layer chromatography combined to mass spectrometry and/or ultraviolet detection and (ii) solid-phase extraction coupled with fractionation on high-performance liquid chromatography. Different chromatographic conditions are tested for each approach. The solid-phase extraction combined with high-performance liquid chromatography fractionation approach was preferred as it offered a greater yield, was less time-consuming and allowed us to selectively isolate marinobufagenin. Both protocols aim to provide efficient and convenient methods for toad venom extraction, based on an easily automatable and systematized strategy.

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