Antitumor activity of extracts from Peperomia elongata
dc.contributor.author | de Castro Campos, Patricia Bonavides | |
dc.contributor.author | Torres Gama, Juliana Julian [UNESP] | |
dc.contributor.author | Pereira, Licia Pacheco | |
dc.contributor.author | Costa-Lotufo, Leticia Veras | |
dc.contributor.author | de Moraes, Manoel Odorico | |
dc.contributor.author | Guimaraes, Elsie Franklin | |
dc.contributor.author | Kato, Massuo Jorge | |
dc.contributor.author | Furlan, Maysa [UNESP] | |
dc.contributor.author | Pessoa, Claudia | |
dc.contributor.institution | Universidade Federal do Ceará (UFC) | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Inst Pesquisas Jardim Bot Rio de Janeiro | |
dc.contributor.institution | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2014-05-20T15:27:34Z | |
dc.date.available | 2014-05-20T15:27:34Z | |
dc.date.issued | 2007-01-01 | |
dc.description.abstract | The cytotoxic potential of ethanol extracts from Peperomia elongata H. B. & K. (Piperaceae) were evaluated against human cancer cell lines by the MTT method. The samples considered cytotoxic were tested for antimitotic activity with the sea urchin egg development test and for hemolytic activity using mice erythrocytes. The extracts from leaves (hexane), stems (ethanol, hexane, hexane: AcOEt, AcOEt, and MeOH: H2O insoluble), and roots (R4) presented potential cytotoxic action. The stems extracts showed the highest toxicity in all tumor cell lines tested, with an IC50 <= 9.0 mu g/mL for ethanol extract, IC50 <= 11.6 mu g/mL for MeOH:H2O insoluble, IC50 <= 7.3 mu g/mL for hexane extract, IC50 <= 11.4 mu g/mL for hexane: AcOEt, and IC50 <= 16.2 mu g/mL for AcOEt extract. All extracts considered cytotoxic for tumoral cell lines presented antimitotic activity. The samples from roots (R4) and stems (ethanol, MeOH: H2O insoluble, and hexane extract from leaves) were found to possess lytic activity in mice erythrocytes but in higher doses (> 125 mu g/mL). Further studies for the isolation and identification of the active principles of these extracts should be undertaken. | en |
dc.description.affiliation | Univ Fed Ceara, Expt Oncol Lab, Fortaleza, Ceara, Brazil | |
dc.description.affiliation | Univ Estadual Paulista, Inst Quim, Araraquara, SP, Brazil | |
dc.description.affiliation | Inst Pesquisas Jardim Bot Rio de Janeiro, Rio de Janeiro, Brazil | |
dc.description.affiliation | Univ São Paulo, Inst Quim, São Paulo, Brazil | |
dc.description.affiliationUnesp | Univ Estadual Paulista, Inst Quim, Araraquara, SP, Brazil | |
dc.format.extent | 760-765 | |
dc.identifier | http://dx.doi.org/10.1080/13880200701585857 | |
dc.identifier.citation | Pharmaceutical Biology. Philadelphia: Taylor & Francis Inc., v. 45, n. 10, p. 760-765, 2007. | |
dc.identifier.doi | 10.1080/13880200701585857 | |
dc.identifier.issn | 1388-0209 | |
dc.identifier.lattes | 1308042794786872 | |
dc.identifier.uri | http://hdl.handle.net/11449/37519 | |
dc.identifier.wos | WOS:000251972600006 | |
dc.language.iso | eng | |
dc.publisher | Taylor & Francis Inc | |
dc.relation.ispartof | Pharmaceutical Biology | |
dc.relation.ispartofjcr | 1.918 | |
dc.relation.ispartofsjr | 0,563 | |
dc.rights.accessRights | Acesso restrito | pt |
dc.source | Web of Science | |
dc.subject | antitumor | pt |
dc.subject | cytotoxic activity | pt |
dc.subject | MTT assay | pt |
dc.subject | Peperomia | pt |
dc.subject | piperaceae | pt |
dc.title | Antitumor activity of extracts from Peperomia elongata | en |
dc.type | Artigo | pt |
dcterms.license | http://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp | |
dcterms.rightsHolder | Taylor & Francis Inc | |
dspace.entity.type | Publication | |
relation.isOrgUnitOfPublication | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
relation.isOrgUnitOfPublication.latestForDiscovery | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
unesp.author.lattes | 1308042794786872 | |
unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Química, Araraquara | pt |
unesp.department | Química Orgânica - IQAR | pt |
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