Ping Zhou
Xi'an Jiaotong University
6 Papers
21 Citations
Ping Zhou is an academic researcher from Xi'an Jiaotong University. The author has contributed to research in topics: Houttuynia cordata & Chelerythrine. The author has an hindex of 5, co-authored 6 publications.
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Papers
A Combined Peritoneal Macrophage/Cell Membrane Chromatography and Offline GC–MS Method for Screening Anti-Inflammatory Components from Chinese Traditional Medicine Houttuynia cordata Thunb.
TL;DR: The major component retained by CMC was identified as methyl nonyl ketone (MNK) by GC–MS, and in vitro experiments revealed that MNK was able to inhibit LPS-induction of TNF-α, NO, and H2O2 production in a dose-dependent manner.
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The pharmacokinetics of chelerythrine solution and chelerythrine liposomes after oral administration to rats.
TL;DR: Results showed that the chelerythrine-liposome has been successfully prepared by the emulsion/solvent evaporation method, and it can be concluded that incorporation into liposomes prolonged chelersythrine retention within the systemic circulation.
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Determination of 2-undecanone in rat plasma and tissue by a high performance liquid chromatography method: an application for the pharmacokinetic and tissue distribution research
TL;DR: In this paper, a reliable high performance liquid chromatography (HPLC) method was established to investigate the pharmacokinetic and tissue distribution profiles of 2-undecanone.
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Effects of chelerythrine, a specific inhibitor of cyclooxygenase-2, on acute inflammation in mice
TL;DR: Results clearly suggested that CHE is a bioactive agent which has a significant anti-inflammatory action, which may be relevant to the inhibition of the release/production of exudates and prostaglandin E(2) mediated through cyclooxygenase-2 regulation.
Houttuynia cordata Thunb. Volatile Oil Exhibited Anti‐inflammatory Effects In Vivo and Inhibited Nitric Oxide and Tumor Necrosis Factor‐α Production in LPS‐stimulated Mouse Peritoneal Macrophages In Vitro
TL;DR: In vitro exposure of mouse resident peritoneal macrophages to 1, 10, 100 and 1000 µg/mL of HC volatile oil significantly suppressed lipopolysaccharide (LPS)‐stimulated production of NO and tumor necrosis factor‐α (TNF‐α) in a dose‐dependent manner.