Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/61011
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dc.contributor.authorTran, Chieu An-
dc.contributor.authorPham, Hong Ngoc-
dc.contributor.authorPham, Minh Sang-
dc.contributor.authorPham, Ngoc Truc-
dc.contributor.authorNguyen, Huynh Thuy Tien-
dc.contributor.authorTran, Phan Huynh Nhu-
dc.contributor.authorPhan, Thi Thanh Tam-
dc.contributor.authorLe, Ngoc Hung-
dc.contributor.authorPhung, Van Trung-
dc.date.accessioned2021-08-11T03:23:49Z-
dc.date.available2021-08-11T03:23:49Z-
dc.date.issued2021-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/61011-
dc.description.abstractOstruthin was successfully isolated from the extract of Paramignya trimera (Oliver) Burkill roots by centrifugal partition chromatography (CPC) in one run. The two-phase solvent system composed of n-hexane-ethyl acetate- methanol-water (2:1:2:1 v/v) in ascending mode (the upper organic phase was the mobile phase), with flow rate of 8.0 (mL/min) and rotation speed of 1600 rpm, was used. The purity of the ostruthin after isolation is 97.5 % confirmed by HPLC-DAD at 320 nm. The present study highlights the ability of a CPC system to obtain high purity ostruthin directly from the P. trimera roots ethyl acetate extract.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesVietnam Journay of Chemistry;No.59(1) .- P.69-72-
dc.subjectParamignya trimera rootsvi_VN
dc.subjectCPCvi_VN
dc.subjectHPLC-DADvi_VN
dc.subjectOstruthinvi_VN
dc.subjectPurificationvi_VN
dc.titleDirectly Purification of Ostruthin from Paramignya trimera roots by CPC (centrifugal partition chromatography)vi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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