http://dx.doi.org/10.4314/tjpr.v12i4.13
Abstract
Purpose: To isolate and identify
the cytotoxicity of the constituents of Sarcopyramis
bodinieri var. delicate.
Methods: S. bodinieri var. delicate
was extracted with hydrochloric acid-methanol and
fractionated with ethyl acetate further. The chemical
constituents of the ethyl acetate fraction were purified
by a combination of D101 macroporous resin and Sephadex
LH-20 column chromatography. The structure was
characterized by 1H-Nuclear Magnetic
Resonance (NMR) and electrospray ionization tandem mass
spectrometry (ESI-MS). Apoptosis was evaluated by
fluorescence staining and Western blot analysis using
4,6-diamidino-2-phenylindole (DAPI) staining and poly
(ADP-ribose) polymerase (PARP)
SDS-PAGE tests in HepG2 liver cancer
cells.
Results: One flavonoid with high
purity was purified by the combination of D101
macroporous resin and Sephadex LH-20 column
chromatography. The flavonoid compound was identified as
quercetin by 1H-NMR and ESI-MS analyses. DAPI
staining and PARP SDS-PAGE tests showed 60 mM quercetin
could induce potential apoptotic activity in HepG2 liver
cancer cells.
Conclusion: Quercetin was the major
cytotoxicity constituent in S. bodinieri var. delicate.
Keywords: Apoptotic
activity, Quercetin, Sarcopyramis bodinieri var.
delicate, HepG2 liver cancer cells, Electrospray
ionization tandem