Use este identificador para citar ou linkar para este item: https://repositorio.inpa.gov.br/handle/1/37383
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dc.contributor.authorOliveira, Felipe P. de-
dc.contributor.authorDa, Ana Carolina B.-
dc.contributor.authorde Lima, Emilly J.S.P.-
dc.contributor.authorSilva, Valdenizia Rodrigues-
dc.contributor.authorDe, Luciano-
dc.contributor.authorda Anunciação, Talita A.-
dc.contributor.authorNogueira, Mateus Lima-
dc.contributor.authorSoares, Milena B.P.-
dc.contributor.authorDias, Rosane Borges-
dc.contributor.authorGurgel Rocha, Clarissa Araújo-
dc.contributor.authorDuvoisin Júnior, Sérgio-
dc.contributor.authorAlbuquerque, Patricia M.-
dc.contributor.authorLima, Emerson Silva-
dc.contributor.authorGonçalves, José Francisco de Carvalho-
dc.contributor.authorBataglion, Giovana Anceski-
dc.contributor.authorCosta, Emmanoel Vilaca̧-
dc.contributor.authorda Silva, Felipe Moura Araújo-
dc.contributor.authorKoolen, Hector H.F.-
dc.contributor.authorBezerra, D. P.-
dc.date.accessioned2021-04-09T18:19:17Z-
dc.date.available2021-04-09T18:19:17Z-
dc.date.issued2021-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/37383-
dc.description.abstractAniba parviflora (Meisn.) Mez (Lauraceae) is an aromatic plant of the Amazon rainforest, which has a tremendous commercial value in the perfumery industry; it is popularly used as flavoring sachets and aromatic baths. In Brazilian folk medicine, A. parviflora is used to treat victims of snakebites. Herein, we analyzed the chemical composition of A. parviflora bark essential oil (EO) and its effect on the growth of human hepatocellular carcinoma HepG2 cells in vitro and in vivo. EO was obtained by hydrodistillation and characterized by GC-MS and GC-FID. The main constituents of EO were linalool (16.3±3.15), α-humulene (14.5±2.41 %), δ-cadinene (10.2±1.09 %), α-copaene (9.51±1.12 %) and germacrene B (7.58±2.15 %). Initially, EO's cytotoxic effect was evaluated against five cancer cell lines (HepG2, MCF-7, HCT116, HL-60 and B16-F10) and one non-cancerous one (MRC-5), using the Alamar blue method after 72 h of treatment. The calculated IC50 values were 9.05, 22.04, >50, 15.36, 17.57, and 30.46 μg/mL, respectively. The best selectivity was for HepG2 cells with a selective index of 3.4. DNA Fragmentation and cell cycle distribution were quantified in HepG2 cells by flow cytometry after a treatment period of 24 and 48 h. The effect of EO on tumor development in vivo was evaluated in a xenograft model using C.B-17 SCID mice engrafted with HepG2 cells. In vivo tumor growth inhibition of HepG2 xenograft at the doses of 40 and 80 mg/kg were 12.1 and 62.4 %, respectively.en
dc.relation.ispartofVolume 18, Número 3pt_BR
dc.subjectAniba parvifloraen
dc.subjectHepG2en
dc.subjectLauraceaeen
dc.subjectantitumor agentsen
dc.subjectcytotoxicityen
dc.titleEssential Oil from Bark of Aniba parviflora (Meisn.) Mez (Lauraceae) Reduces HepG2 Cell Proliferation and Inhibits Tumor Development in a Xenograft Modelen
dc.typeArtigopt_BR
dc.identifier.doi10.1002/cbdv.202000938-
dc.publisher.journalChemistry and Biodiversityen
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