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A new cytotoxic flavonoid from the fruit of Sinopodophyllum hexandrum.
TLDR
A new flavonoid, 8,2'-diprenylquercetin 3-methyl ether exhibited cytotoxic activities against MDA-231 and T47D breast cancer cell lines and was isolated from Sinopodophylli Fructus for the first time.
[Immune regulating activity of a novel organoselenium compound ethaselen-1 in C57/BL mice].
TLDR
The novel organoselenium compound Eb1 has immune regulating activity in vivo, and could obviously increase the relative weight of spleen and increase LAK cell activity of LLC mice.
Flavonoids isolated from Sinopodophylli Fructus and their bioactivities against human breast cancer cells.
TLDR
Four prenylated flavonoids compounds 1-4, named sinopodophyllines A-D, and a flavonoid glycoside (compound 13), sinopODophylliside A, together with 19 known compounds were isolated from the fruits of Sinopodphyllum hexandrum.
[Cytological study on osteoblasts and in-situ setting calcium phosphate cements].
TLDR
The process of solidification of the three kinds of CPC pastes has the toxic effect on cells, which is irreversible and further study needs to explore a method to protect osteoblasts when seeded into the CPC paste.
[The antitumor activity of Shuang-Xi-Zuo-Wan-1 in C57/BL mice].
TLDR
The novel organoselenium compound Eb has antitumor activity in vivo, which can inhibit the growth and infiltration of LLC in mice, and induce the apoptosis of cancer cells.
[Culture of osteoblasts by serial explant culture and comparison of their characteristics].
TLDR
Investigation of a simple, economical and efficient method of primary osteoblast culture found it can harvest the same kind of osteoblasts as the explant culture, and more osteoblast can be obtained at a single time.
[Development of a novel in-vitro culture device simulating distraction osteogenesis and expression of osteoblast cytoskeleton].
TLDR
The novel in vitro culture device simulating distraction osteogenesis is suitable for the study of distraction osteogenic in vitro and results in reorganization and disruption of actin cytoskeleton.