2013
DOI: 10.1016/j.jep.2012.12.010
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Development of an SPE–HPLC–MS method for simultaneous determination and pharmacokinetic study of bioactive constituents of Yu Ping Feng San in rat plasma after oral administration

Abstract: This analytical method is a selective, sensitive, precise, accurate, and reliable assay for simultaneous determination of cycloastragenol, calycosin, formononetin, GMV, and cimifugin in rat plasma.

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Cited by 17 publications
(9 citation statements)
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“…In pharmacokinetic studies, oral administration of a cimifugin-containing crude drug to rats resulted in a high concentration of cimifugin in the blood [ 13 , 14 ]. For instance, cimifugin was measured at 881–1510 ng/mL in the blood of rats given a traditional Chinese medicine (Yu Ping Feng San) [ 33 ]. Cimifugin suppressed nitric oxide production by murine macrophages and exhibited 1,1-diphenyl-2-picrylhydrazyl free-radical scavenging activity in a cell-free bioassay system [ 34 ].…”
Section: Discussionmentioning
confidence: 99%
“…In pharmacokinetic studies, oral administration of a cimifugin-containing crude drug to rats resulted in a high concentration of cimifugin in the blood [ 13 , 14 ]. For instance, cimifugin was measured at 881–1510 ng/mL in the blood of rats given a traditional Chinese medicine (Yu Ping Feng San) [ 33 ]. Cimifugin suppressed nitric oxide production by murine macrophages and exhibited 1,1-diphenyl-2-picrylhydrazyl free-radical scavenging activity in a cell-free bioassay system [ 34 ].…”
Section: Discussionmentioning
confidence: 99%
“…The rats were fasted overnight and injected a dose of 132.8 mg/kg. Blood samples (about 2.0 mL) from intraocular angular vein of rats were collected and placed into EDTA-2Na anticoagulant tubes at predetermined interval times (5,10,20,30,60,90,120,180, and 240 min). Then, blood samples were centrifuged at 3800 rpm for 10 min, and the separated plasma samples were stored at −20 ∘ C for next analysis.…”
Section: Animal Administration and Samplingmentioning
confidence: 99%
“…It can explain the variation of the intensity of the pharmacological effects and explore many in vivo key issues during a pharmacokinetics study, such as absorption and distribution of chemical drugs, bioavailability, biotransformation and excretion pathway. As for TCM, only one or more effective components with known chemical structures in mixtures were selected as targets to investigate the pharmacokinetics by determining the individual metabolomic component concentration in the blood, which is the same as the method of western chemical drugs' pharmacokinetics studies [7][8][9][10]. Even if a single herb of TCM contains dozens or hundreds of kinds of chemical components [11,12], not to mention the Chinese herbal formula [13,14], some individual metabolomic components' in vivo tests cannot represent pharmacokinetics process of TCM with complicated multicomponents and cannot clarify the relationship between a variety of components and integral efficacy [15].…”
Section: Introductionmentioning
confidence: 99%
“…Some analytical techniques based on LC-MS have been reported for the detection of several high-abundance components and their counterparts in YPF in biological samples [ 21 , 22 ]. Most of these reports are focused on one kind of compound in single herbal plant of YPF, especially Astragali radix and Saposhnikoviae radix , using the most abundant compounds such as saponins and their aglycones as chemical markers [ 23 ]. Only a small number of reports are available on the simultaneous analysis of the bioactive constituents in Atractylodis rhizoma , such as atractylenolide I–III [ 24 , 25 , 26 ], as its low content and similar retention behaviors make the detection difficult.…”
Section: Introductionmentioning
confidence: 99%