2016
DOI: 10.1016/j.msec.2016.03.094
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Development and pharmacological evaluation of in vitro nanocarriers composed of lamellar silicates containing copaiba oil-resin for treatment of endometriosis

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Cited by 19 publications
(6 citation statements)
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“…The oral administration of copaiba has been used as another form of alternative therapy with controversial results. With 28.6%, in the present meta-analysis, the oral administration of copaiba has been shown to be an effective agent against certain parasites, 14 gastrointestinal cancer, 8 6,7,15 arthritis, 16 and other conditions. Contrary to what was thought, the oral administration of copaiba was shown to be non-toxic to rat liver when used as a carrier for amphotericin B.…”
Section: Resultsmentioning
confidence: 72%
“…The oral administration of copaiba has been used as another form of alternative therapy with controversial results. With 28.6%, in the present meta-analysis, the oral administration of copaiba has been shown to be an effective agent against certain parasites, 14 gastrointestinal cancer, 8 6,7,15 arthritis, 16 and other conditions. Contrary to what was thought, the oral administration of copaiba was shown to be non-toxic to rat liver when used as a carrier for amphotericin B.…”
Section: Resultsmentioning
confidence: 72%
“…2A, free DETC presents characteristic peaks at 837, 909, 985 cm -1 (CeS), 1070, 2104 (C]S) and 1423 cm −1 N-CS 2 ) [11,40,41]. Copaiba oil presents a characteristic peak at 1740 cm -1 (C] O) and a broad medium band between 3100 and 2700 cm -1 , attributed to carboxylic acids [42,43]. In the FTIR spectra of beeswax, it was observed peaks at 2922, 2848 cm -1 (stretching vibrations of CeH groups), 1736 cm −1 (stretching vibrations of the carbonyls of esters), 1467 cm -1 (hydrocarbon vibrations) and peaks located at 1300 to 728 cm -1 related to the ester group [44,45].…”
Section: Resultsmentioning
confidence: 99%
“…[ 200 ] Therefore, several research groups proposed that encapsulating copaiba oil extracts within nanomaterials may provide advantages for their bioavailability, delivery, safety, and therapeutic effect. [ 43,45,44 ]…”
Section: Nanoparticle‐based Treatment Modalitiesmentioning
confidence: 99%
“…In contrast to CPO‐loaded PLGA nanoparticles, the same research group demonstrated that copaiba oleoresin encapsulated in a non‐toxic lamellar silicate nanocomposite (Viscogel B8, VB8) significantly reduces the cell viability and proliferation of all three endometrial cell lines (CESCs, EuESCs, and EctESCs). [ 43 ] Moreover, the observed therapeutic effect of COPA nanocomposites was the most pronounced in the endometrial stromal cells obtained from endometriotic lesions (EctESCs). For example, a 60% reduction in proliferation of EctESCs was observed when treated with 300 µg mL −1 VB8 COPA nanocomposite, while the proliferation of CESCs and EuSCs decreased by 20% and 35%, respectively, with the same formulation and concentration.…”
Section: Nanoparticle‐based Treatment Modalitiesmentioning
confidence: 99%