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Title: | Cytotoxic fractions from the leaves of Tachia grandiflora |
Authors: | Pohlit, Adrian Martin Tigre, Ryuga Frota Coelho Cavalcanti, Bruno Moraes, Manœl Odorico de Costa-Lotufo, Leticia Veras Moraes, Maria Elisabete Amaral de Santos, Elba Vieira Mustafa dos Morais, Sabrina Kelly Reis Nunomura, Sergio Massayoshi Pessoa, Cláudia Ó. |
Keywords: | Alcohol Butanol Chloroform Doxorubicin Hexane Methanol Plant Extract Silica Gel Tachia Grandiflora Extract Unclassified Drug Water Animals Cell Antineoplastic Activity Breast Tumor Cancer Inhibition Cell Strain Hl 60 Cell Strain Mcf 7 Colon Tumor Column Chromatography Concentration Response Confidence Interval Controlled Study Cytolysis Drug Activity Drug Cytotoxicity Drug Isolation Drug Research Drug Screening Drug Synthesis Hemolysis Human Human Cell Ic 50 In Vitro Study Leukemia Medicinal Plant Melanoma B16 Mouse Nonhuman Plant Leaf Plant Stem Tachia Grandiflora Cell Line, Tumor Gentianaceae Murinae Tachia Grandiflora |
Issue Date: | 2007 |
metadata.dc.publisher.journal: | Pharmaceutical Biology |
metadata.dc.relation.ispartof: | Volume 45, Número 5, Pags. 429-433 |
Abstract: | This 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. |
metadata.dc.identifier.doi: | 10.1080/13880200701215422 |
Appears in Collections: | Artigos |
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