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Métodos Terapêuticos e Terapias MTCI
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1.
Phytochem Anal ; 34(5): 560-570, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-37202874

RESUMO

INTRODUCTION: Lanqin Oral Liquid (LQL) is a traditional Chinese medicine preparation (TCMP) containing five herbal medicines and has been commonly used for the treatment of pharyngitis and hand-foot-and-mouth disease in clinic. The material basis of LQL has been reported in our previous study, but the contents of the major components and the features of saccharide in LQL are still unclear. OBJECTIVES: This study aimed to establish accurate and rapid methods for the quantification of the major components and profiling of saccharide in LQL. The quantitative results combined with similarity evaluation were applied to improve the quality control of LQL. METHODOLOGY: An ultra-high performance liquid chromatography coupled with triple-quadrupole tandem mass spectrometry (UPLC-QQQ-MS) method was utilised to determine 44 major components. Cosine similarity was used to evaluate the similarities among 20 batches of LQL based on the quantitative results of 44 major components. The physicochemical properties, structure, composition, and contents of saccharide in LQL were detected by a combination of chemical and instrumental analysis. RESULTS: A total of 44 compounds, including flavonoids, iridoid glycosides, alkaloids, and nucleosides, were accurately determined. The 20 batches of LQL were remarkably similar (> 0.95). In addition, d-glucose, galactose, d-glucuronic acid, arabinose, and d-mannose were detected in saccharide of LQL. The contents of saccharide in LQL were 13.52-21.09 mg/ml. CONCLUSIONS: The established methods can be applied for the comprehensive quality control of LQL, including characterisation of saccharide and quantification of representative components. Our study will provide a robust chemical foundation for disclosing the quality markers of its therapeutic effect.


Assuntos
Medicamentos de Ervas Chinesas , Medicamentos de Ervas Chinesas/química , Medicina Tradicional Chinesa , Espectrometria de Massas em Tandem/métodos , Flavonoides/análise , Controle de Qualidade , Cromatografia Líquida de Alta Pressão/métodos
2.
Zhong Yao Cai ; 37(2): 240-2, 2014 Feb.
Artigo em Chinês | MEDLINE | ID: mdl-25095343

RESUMO

OBJECTIVE: To study the chemical constituents from the leaf of Bombax ceiba. METHODS: The compounds were isolated and purified with silica gel and Sephadex LH-20 column chromatography. Their structures were determined on the basis of physicochemical properties and spectroscopic analysis. RESULTS: Eleven compounds were isolated and identified as taraxeryl acetate (1), squalene (2), taraxerone (3), beta-sitosterol palmitate (4), taraxerol (5), 4-methyl stigmast-7-en-3-ol (6), 1H-indole-3-carboxylic acid (7), 6-O-palmitoylsitosteryl-D-glucoside (8), 12beta-hydroxyl-pregnane-4, 16-diene-3, 20-dione (9), loliolide (10) and 5-(hydroxymethyl) furfural (11). CONCLUSION: All the compounds are isolated from this genus for the first time.


Assuntos
Bombax/química , Medicamentos de Ervas Chinesas/química , Folhas de Planta/química , Cromatografia em Camada Fina , Medicamentos de Ervas Chinesas/isolamento & purificação , Estrutura Molecular , Ácido Oleanólico/análogos & derivados , Ácido Oleanólico/química , Ácido Oleanólico/isolamento & purificação , Sitosteroides/química , Sitosteroides/isolamento & purificação , Esqualeno/química , Esqualeno/isolamento & purificação , Triterpenos/química , Triterpenos/isolamento & purificação
3.
Zhongguo Zhong Yao Za Zhi ; 38(2): 204-7, 2013 Jan.
Artigo em Chinês | MEDLINE | ID: mdl-23672042

RESUMO

OBJECTIVE: To study the chemical constituents in the seeds of Oroxylum indicum. METHOD: Twenty compounds were isolated and purified by silica gel, and Sephadex LH-20 column chromatography, and their structures were determined by spectroscopic analysis including NMR and MS. RESULT: Twenty compounds were isolated and identified as oroxin A (1), oroxin B (2), chrysin (3), baicalein (4), quercetin (5), apigenin (6), kaempferol (7), quercetin-3-O-ara-binopyranoside (8), lupeol C9), lup-20 (29)-ene-2alpha,3beta-diol (10), pinosylvin (11), dihydropinosylvin (12), cholest-5-ene-3, 7-diol (13), rengyol (14), isorengyol (15), zarzissine (16), (E) -pinosylvin-3-O-beta-D-glucopyranoside (17), adenosine (18), sitosterol (19) and daucosterol (20). CONCLUSION: Compounds 11-13 and 15-18 were obtained from the genus Oroxylum for the first time, and except compound 18, the remaining 6 compounds were obtained from the family Bignoniaceae for the first time.


Assuntos
Bignoniaceae/química , Medicamentos de Ervas Chinesas/química , Sementes/química , Cromatografia , Medicamentos de Ervas Chinesas/isolamento & purificação , Espectroscopia de Ressonância Magnética , Espectrometria de Massas
4.
J Asian Nat Prod Res ; 14(5): 491-5, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22423627

RESUMO

A new eudesmane sesquiterpene glycoside, ophiopogonoside B (1), along with five known compounds, ophiopogonoside A (2), ruscogenin-1-O-[ß-D-glucopyranosyl (1 → 2)]-[ß-D-xylopyranosyl (1 → 3)]-ß-D-fucopyranoside (3), palmitic acid (4), palmitic acid glyceride (5), and ß-sitosterol-D-glucopyranoside (6),was isolated from the tuberous roots of Liriope muscari (Decn.) Bailey (Liliaceae). Their structures were confirmed by 1D and 2D NMR spectroscopy. Among them, compounds 1, 2, 4, and 5 were the first reported from the genus Liriope. Ophiopogonoside B (1) showed moderate inhibitory activity to glycogen phosphorylase a.


Assuntos
Medicamentos de Ervas Chinesas/isolamento & purificação , Glicogênio Fosforilase/efeitos dos fármacos , Glicosídeos/isolamento & purificação , Liriope (Planta)/química , Sesquiterpenos de Eudesmano/isolamento & purificação , Algoritmos , Animais , Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/farmacologia , Glicogênio Fosforilase/metabolismo , Glicosídeos/química , Glicosídeos/farmacologia , Fígado/enzimologia , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Raízes de Plantas/química , Coelhos , Sesquiterpenos de Eudesmano/química , Sesquiterpenos de Eudesmano/farmacologia , Estereoisomerismo
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