Molecules (Jan 2022)

Bioassay-Guided Fractionation of <i>Siparuna glycycarpa</i> <i>n</i>-Butanol Extract with Inhibitory Activity against Influenza A(H1N1)pdm09 Virus by Centrifugal Partition Chromatography (CPC)

  • Carla Monteiro Leal,
  • Suzana Guimarães Leitão,
  • Leonardo Luiz Oliveira de Mello,
  • Isabel de Castro Rangel,
  • Carlos Vinicius Azevedo da Silva,
  • Milene Dias Miranda,
  • Amanda Resende Tucci,
  • Camilla Blanco de Assis,
  • Carolina de Queiroz Sacramento,
  • Natalia Fintelman-Rodrigues,
  • Hector Henrique Ferreira Koolen,
  • Boniek Gontijo Vaz,
  • Rosineide Costa Simas,
  • Gilda Guimarães Leitão

DOI
https://doi.org/10.3390/molecules27020399
Journal volume & issue
Vol. 27, no. 2
p. 399

Abstract

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Siparuna glycycarpa occurs in the Amazon region, and some species of this genus are used in Brazilian folk medicine. A recent study showed the inhibitory effect of this species against influenza A(H1N1)pdm09 virus, and in order to acquire active fractions, a polar solvent system n-butanol-methanol-water (9:1:10, v/v) was selected and used for bioassay-guided fractionation of n-butanol extract by centrifugal partition chromatography (CPC). The upper phase was used as stationary phase and the lower phase as mobile (descending mode). Among the collected fractions, the ones coded SGA, SGC, SGD, and SGO showed the highest antiviral inhibition levels (above 74%) at 100 µg·mL−1 after 24 h of infection. The bioactive fractions chemical profiles were investigated by LC-HRMS/MS data in positive and negative ionization modes exploring the Global Natural Products Social Molecular Networking (GNPS) platform to build a molecular network. Benzylisoquinoline alkaloids were annotated in the fractions coded SGA, SGC, and SGD collected during elution step. Aporphine alkaloids, O-glycosylated flavonoids, and dihydrochalcones in SGO were acquired with the change of mobile phase from lower aqueous to upper organic. Benzylisoquinolinic and aporphine alkaloids as well as glycosylated flavonoids were annotated in the most bioactive fractions suggesting this group of compounds as responsible for antiviral activity.

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