Untargeted UHPLC-Q-Exactive Orbitrap MS and Targeted UHPLC-QqQ-MS/MS for Exploring the Effective Components of "Wen Tong Plaster" Cataplasm in Treating Rats With Primary Dysmenorrhea

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This study analyzed the chemical composition and transdermal delivery of Wen Tong Plaster in rats with primary dysmenorrhea, identifying four key bioactive components that reach uterine tissue and bind to cytochrome P450 1A1.

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Abstract

"Wen Tong Plaster" is renowned for its therapeutic effects of warming meridians, dispelling cold, and promoting blood circulation. However, its chemical composition and active pharmacological substances have yet to be fully elucidated. In this study, the chemical components of "Wen Tong Plaster" cataplasm and the transdermal components in vivo and in vitro were comprehensively analyzed by mass spectrometry targeted quantification method, and the release kinetics of the main transdermal components in vitro were evaluated, and the concentration-time variation of key active transdermal components in vivo was studied, finally molecular docking technology was used to predict the mechanism of action of key bioactive transdermal components. Using UHPLC-Q-Exactive Orbitrap MS, a total of 129 plant chemical components were found in the "Wen Tong Plaster" cataplasm extract, with 41 components detected as in vitro transdermal compounds. In subcutaneous tissue and uterine tissue, 53 and 36 in vivo transdermal components were characterized, respectively. The release kinetics of "Wen Tong Plaster" cataplasm were evaluated by tetrahydropalmatine, corydaline, and dihydrotanshinone I, three marker components, and fitted to a first-order kinetic model based on integrated release kinetics. After "Wen Tong Plaster" cataplasm administration, tetrahydropalmatine, corydaline, dihydrotanshinone I, and α-cyperone were accurately quantified in the subcutaneous tissue, plasma, and uterus tissue by UHPLC-QqQ-MS/MS, while the concentration-time changes of them in the subcutaneous tissue, plasma, and uterus tissue were investigated. The molecular docking results indicated that all four components exhibited favorable binding affinity with the targets, particularly demonstrating strong binding capacity to the cytochrome P450 1A1 target, suggesting it as a potential therapeutic target for "Wen Tong Plaster" cataplasm. In summary, the study revealed the pharmacodynamic material basis and in vitro release kinetics of "Wen Tong Plaster" cataplasm, providing a theoretical foundation and data support for further research on the mechanism of action and clinical application.

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MeSH descriptors

Drugs, Chinese Herbal Drugs, Chinese Herbal Drugs, Chinese Herbal Drugs, Chinese Herbal Drugs, Chinese Herbal Animals Chromatography, High Pressure Liquid Female Molecular Docking Simulation Rats Rats, Sprague-Dawley Tandem Mass Spectrometry

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SciLite annotations

organisms 25
mosquito plant rattus sp. primulina sp. 'dongguanica' corydalis yanhusuo rhizoma peanut ligusticum chuanxiong cyperus rotundus cinnamon cinnamomum cassia psylla evodiae tetradium ruticarpum zingiber cyperus rhizomaticola zingiber officinale corydalis sp. salvia miltiorrhiza tetradium ruticarpum zitter rats rodents multicellular animals rattus sp. human mus sp. noordeloos 2009062
chemicals 42
tetrahydropalmatine corydaline dihydrotanshinone i tetrahydropalmatine alkaloid fructuronic acids sterol anthraquinone nucleotide polysaccharide octahydronaphthalenes tetracyclic diterpenoid ferulic acids terpene flavonoids evodiamine tetrahydropalmatine cinnamaldehydes cinnamyl alcohol cinnamic acid isotanshinone iib salvianolic acid b corydaline dihydrotanshinone i puerarin acetonitrile methanol formic acid water nitrogen isoflurane sodium sulfide hydroquinones phenylpropanoid phenols amine alkaloid quinone dihydroxyquinoline ibuprofen diclofenac sodium

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