Abstract
Hot water-soluble crude polysaccharides were extracted from the rhizomes of wild turmeric, Curcuma aromatica Salisb. (Zingiberaceae), using dry grinding, boiling water extraction, and then ethanol precipitation. The crude polysaccharide extract was then fractionated by DEAE-cellulose ion exchange column chromatography, and subsequently further purified by Superdex G-200 gel filtration column chromatography, giving two relatively abundant polysaccharide fractions, called P11 and P21, and a much less common fraction P22 obtained in insufficient amounts for further analysis. The two main polysaccharide fractions were evaluated for monosaccharide composition by acid hydrolysis and high performance liquid chromatography (HPLC), whilst the molecular weight and functional groups were determined by gel permeable chromatography (GPC) and FT-IR, respectively. Fractions P11 and P21 were found to be polyxyloses with molecular weight-averages of 469,171 and 157,665Da, respectively. P11 (100μg/mL) could significantly induce human gingival fibroblast cells proliferation by 30%, while P21 (100μg/mL) could significantly inhibit gingival fibroblast cells proliferation by 92%. The in vitro human primary gingival fibroblast cell proliferation in cell culture at a concentration of 100μg/mL. © 2010 Informa UK Ltd.
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Niyomploy, P., Thunyakitpisal, P., Karnchanatat, A., & Sangvanich, P. (2010). Cell proliferative effect of polyxyloses extracted from the rhizomes of wild turmeric, Curcuma aromatica. Pharmaceutical Biology, 48(8), 932–937. https://doi.org/10.3109/13880200903305518
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