2017
DOI: 10.1016/j.mrgentox.2017.05.001
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Copaifera multijuga oleoresin and its constituent diterpene (−)-copalic acid: Genotoxicity and chemoprevention study

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Cited by 13 publications
(10 citation statements)
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“…The identification of the plant material was undertaken by Silvana Tavares Rodrigues at the Herbarium of the Brazilian Agricultural Research Corporation (EMBRAPA) in Belém, Pará, Brazil, where a voucher specimen was deposited under the number NID: 62/2013. Isolation of (−)-copalic acid from C. multijuga oleoresin and its identification The chromatographic process to isolate CA was previously reported by Alves et al (2017). Briefly, 100 g of crude oleoresin were fractionated on Vacuum Liquid Chromatography using a gradient elution with hexanes and ethyl acetate.…”
Section: Collection Of Oleoresin Isolation and Identification Of (−)mentioning
confidence: 99%
“…The identification of the plant material was undertaken by Silvana Tavares Rodrigues at the Herbarium of the Brazilian Agricultural Research Corporation (EMBRAPA) in Belém, Pará, Brazil, where a voucher specimen was deposited under the number NID: 62/2013. Isolation of (−)-copalic acid from C. multijuga oleoresin and its identification The chromatographic process to isolate CA was previously reported by Alves et al (2017). Briefly, 100 g of crude oleoresin were fractionated on Vacuum Liquid Chromatography using a gradient elution with hexanes and ethyl acetate.…”
Section: Collection Of Oleoresin Isolation and Identification Of (−)mentioning
confidence: 99%
“…Furtado et al [28] showed no genotoxic effects in both in vitro and in vivo micronucleus assays using different concentrations of C. multijuga leaf extracts and oleoresin. No genotoxic effects were also observed by Alves et al [29] in their micronucleus tests with C. multijuga oleoresin.…”
Section: /8mentioning
confidence: 55%
“…To date, there are few reports in the literature related to the use of C.O as P.E (Quiñones et al ., 2017, epub ahead of print). However, studies on commercial product safety reveal that this substance is not genotoxic or mutagenic and has shown to be safe after topical application …”
Section: Discussionmentioning
confidence: 99%
“…To date, there are few reports in the literature related to the use of C.O as P.E (Quiñones et al, 2017, epub ahead of print). However, studies on commercial product safety reveal that this substance is not genotoxic or mutagenic [55,63] and has shown to be safe after topical application. [64] Altogether, the results obtained with formulation F4, composed of 2% Cxb and 25% C.O in PEG-400/PG, indicate that it is suitable for the treatment of superficial inflammation of the skin (including skin cancer induced by UVB) and inflammation process from rheumatoid arthritis.…”
Section: Discussionmentioning
confidence: 99%