dc.contributorJátiva, Cumandá
dc.contributorMera, Jacinto
dc.creatorSisalema Sánchez, Diana Elizabeth
dc.date.accessioned2013-07-25T18:44:51Z
dc.date.available2013-07-25T18:44:51Z
dc.date.created2013-07-25T18:44:51Z
dc.date.issued2013-07-25T18:44:51Z
dc.identifierSisalema Sánchez, Diana Elizabeth. (2013). Separación de Metabolitos Secundarios de Martín Galvis (Senna multifuga) con actividad antibacteriana. Escuela Superior Politécnica de Chimborazo. Riobamba.
dc.identifierhttp://dspace.espoch.edu.ec/handle/123456789/2605
dc.description.abstractSeparation of secondary metabolites of Martin Galvis (Senna multijuga with antibacterial activity" aims to extract, purify and possible identification of secondary metabolites in the ethanolic extract and sub extracts this study was conducted in the laboratories of Phytochemistry of the Faculty of Sciences of the Polytechnic School of Chimborazo. The ethanolic extract shows sennosides similar to Sen (Cassia angustifolia). The phytochemical screening indicated that (Senna multijuga) contains anthraquinones, triterpenes, steroids, monoterpenes, sesquiterpene lactones, flavonoids and coumarins. For the separation of these metabolites were used chromatographic methods such as: column chromatography, microcolumn and for the purification preparative plate performing band cutting to subsequently concentrate and check in thin layer chromatography run in solvent systems the most appropriate in which it can demonstrate the 3 chromatographic parameters: efficiency effectiveness, efficiency and resolution subsequently determined in the ultraviolet spectrophotometer. The sub extracts; (II) presents 2 compounds at certain wavelengths(?) max 1=226 nm (coumarin) 2=304 (flavonoid) using solvent of run: Toluene, CH3COOH (93:3. 7), and as developer KOH and EtOAc (100%) developed with CeSO4; the (IV) 2 compounds with wavelengths (?)max 1= 228 nm (ß sitosterol); 2= 276 nm (sesquiterpene lactones) using running solvent EtOAc, MeOH (95:0. 5); EtOAc; Toluene, EtOAc ;(80:2) and as developer solvent Rosentaler and (I) presented 2 compounds at (?)max 1=302 nm (chrysophanol) and 2=313nm using running solvent CH3COOH, EtOAc,1 propanol; (1:40:40) and developed with alcoholic KOH applying the Woodward-Fieser rules it is concluded that it is rehine. It is recommended to deepen this research of these secondary metabolites identified, to be applied in the field of Phytomedicine and Phytotherapy and thus contribute to the development.
dc.languagespa
dc.publisherEscuela Superior Politécnica de Chimborazo
dc.relationUDCTFC;56T00384
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/3.0/ec/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectMETABOLITOS SECUNDARIOS
dc.subjectSEPARACIÓN QUÍMICA
dc.subjectACTIVIDAD ANTIBACTERIANA
dc.subjectMARTIN GALVIS (Senna multifuga)
dc.subjectSENNA MULTIFUGA
dc.titleSeparación de Metabolitos Secundarios de Martín Galvis (Senna multifuga) con actividad antibacteriana
dc.typeTesis


Este ítem pertenece a la siguiente institución