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Isolation and high-performance thin layer chromatographic estimation of Lupeol from Oxystelma esculentum

BACKGROUND: Oxystelma esculentum R. Br. (Family: Asclepiadaceae) is a perennial twiner growing in water-logged areas of the Indian sub-continent. It is used traditionally as a diuretic, laxative and an anti-ulcer agent. However, there is no method available for isolation and estimation of a marker c...

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Detalles Bibliográficos
Autores principales: Pandya, Devang J., Anand, Indermeet S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658039/
https://www.ncbi.nlm.nih.gov/pubmed/23781438
http://dx.doi.org/10.4103/2229-4708.84446
Descripción
Sumario:BACKGROUND: Oxystelma esculentum R. Br. (Family: Asclepiadaceae) is a perennial twiner growing in water-logged areas of the Indian sub-continent. It is used traditionally as a diuretic, laxative and an anti-ulcer agent. However, there is no method available for isolation and estimation of a marker compound from this plant. The present work deals with the isolation and structure elucidation of Lupeol from O. esculentum and high-performance thin layer chromatographic (HPTLC) method development for its estimation. MATERIALS AND METHODS: The petroleum ether extract of the entire plant of O. esculentum was subjected to further fractionation followed by pilot thin layer chromatographic (TLC) experiments and column chromatography. This yielded a pure, white, crystalline solid which resolved at R(f) 0.65 upon TLC of chloroform fraction of the petroleum ether extract using the mobile phase toluene: methanol (9:1). RESULTS: This compound was subjected to ultraviolet (UV), infrared (IR), gas chromatography-mass spectroscopy (GC-MS) and (1) H-nuclear magnetic resonance ((1)H-NMR) spectral analysis and its structure elucidation revealed it to be Lupeol. A novel HPTLC method for the estimation of Lupeol from O. esculentum was developed, in which it was found to be 0.829 ± 0.09% w/w. CONCLUSIONS: The method developed was found to be easy, simple, precise, efficient, accurate, reproducible, specific and sensitive, and could serve as a suitable tool for routine analysis and phytochemical authentication of O. esculentum.