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dc.contributor.authorPohlit, Adrian Martin-
dc.contributor.authorTigre, Ryuga Frota-
dc.contributor.authorCoelho Cavalcanti, Bruno-
dc.contributor.authorMoraes, Manœl Odorico de-
dc.contributor.authorCosta-Lotufo, Leticia Veras-
dc.contributor.authorMoraes, Maria Elisabete Amaral de-
dc.contributor.authorSantos, Elba Vieira Mustafa dos-
dc.contributor.authorMorais, Sabrina Kelly Reis-
dc.contributor.authorNunomura, Sergio Massayoshi-
dc.contributor.authorPessoa, Cláudia Ó.-
dc.date.accessioned2020-06-15T22:02:27Z-
dc.date.available2020-06-15T22:02:27Z-
dc.date.issued2007-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/18656-
dc.description.abstractThis work is part of a larger screening program, which seeks to discover new antitumor plants and compounds from the Brazilian Amazon. In a prescreen of stem and leaf extracts of Tachia grandiflora Maguire & Weaver (Gentianaceae) based on the SRB method, leaf methanol and ethanol extracts showed appreciable cytotoxicity in human breast (MCF-7) and colon (HCT-8) tumor cell lines. Liquid-liquid partitioning of the leaf ethanol extract yielded hexane, chloroform, butanol, and water-methanol fractions. Only the hexane and chloroform fractions were active, inhibiting murine melanoma (B-16) and HCT-8 cells. The chloroform fraction suffered sequential column chromatography on silica gel using different eluent systems and yielded a number of very active subfractions. In all, 25 fractions and subfractions were tested, and 10 exhibited high growth inhibition of HCT-8, and two of these presented strong inhibition of murine melanoma (B-16) cells. The most active subfractions were tested against five tumor cell lines (leukemia CEM and HL-60, as well as the three used previously) using the MTT assay, and four fractions demonstrated significant cytotoxicity based on IC50. Cell lysis was discarded as a possible mechanism for in vitro cytotoxicity given that these fractions did not exhibit hemolytic activity. The greatest antiproliferative potential was found in the second (two samples) and third generation (two samples) chromatographic subfractions of the chloroform fraction (obtained from partitioning of the ethanol extract). These subfractions proved to be complex mixtures from which no pure substance could be isolated after further chromatographic separations. © 2007 Informa Healthcare.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 45, Número 5, Pags. 429-433pt_BR
dc.rightsRestrito*
dc.subjectAlcoholen
dc.subjectButanolen
dc.subjectChloroformen
dc.subjectDoxorubicinen
dc.subjectHexaneen
dc.subjectMethanolen
dc.subjectPlant Extracten
dc.subjectSilica Gelen
dc.subjectTachia Grandiflora Extracten
dc.subjectUnclassified Drugen
dc.subjectWateren
dc.subjectAnimals Cellen
dc.subjectAntineoplastic Activityen
dc.subjectBreast Tumoren
dc.subjectCancer Inhibitionen
dc.subjectCell Strain Hl 60en
dc.subjectCell Strain Mcf 7en
dc.subjectColon Tumoren
dc.subjectColumn Chromatographyen
dc.subjectConcentration Responseen
dc.subjectConfidence Intervalen
dc.subjectControlled Studyen
dc.subjectCytolysisen
dc.subjectDrug Activityen
dc.subjectDrug Cytotoxicityen
dc.subjectDrug Isolationen
dc.subjectDrug Researchen
dc.subjectDrug Screeningen
dc.subjectDrug Synthesisen
dc.subjectHemolysisen
dc.subjectHumanen
dc.subjectHuman Cellen
dc.subjectIc 50en
dc.subjectIn Vitro Studyen
dc.subjectLeukemiaen
dc.subjectMedicinal Planten
dc.subjectMelanoma B16en
dc.subjectMouseen
dc.subjectNonhumanen
dc.subjectPlant Leafen
dc.subjectPlant Stemen
dc.subjectTachia Grandifloraen
dc.subjectCell Line, Tumoren
dc.subjectGentianaceaeen
dc.subjectMurinaeen
dc.subjectTachia Grandifloraen
dc.titleCytotoxic fractions from the leaves of Tachia grandifloraen
dc.typeArtigopt_BR
dc.identifier.doi10.1080/13880200701215422-
dc.publisher.journalPharmaceutical Biologypt_BR
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