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1.
Nat Prod Res ; 33(4): 577-579, 2019 Feb.
Article in English | MEDLINE | ID: mdl-29130346

ABSTRACT

The composition and the antinociceptive activity of the essential oil of Stevia serrata Cav. from a population located in the west highlands of Guatemala were evaluated. A yield of 0.2% (w/w) of essential oil was obtained by hydrodistillation of the dried aerial parts of the plant. The essential oil analysed by GC-FID and GC-MS showed a high content of sesquiterpenoids, with chamazulene (60.1%) as the major component and 91.5% of the essential oil composition was identified. To evaluate antinociceptive activity in mice, the essential oil of S. serrata Cav. was administered as gavage, using three different doses. In the formalin test, the animals were pre-treated with oral doses of the essential oil before the administration of formalin. Oral administration of S. serrata Cav. essential oil produced a marked antinociceptive activity. Therefore, the plant could be domesticated as a source of essential oil rich in chamazulene for developing medicinal products.


Subject(s)
Analgesics/isolation & purification , Oils, Volatile/pharmacology , Stevia/chemistry , Analgesics/chemistry , Analgesics/pharmacology , Animals , Azulenes/analysis , Gas Chromatography-Mass Spectrometry , Guatemala , Mice , Oils, Volatile/chemistry , Pain Measurement , Sesquiterpenes/analysis
2.
Food Chem ; 218: 305-312, 2017 Mar 01.
Article in English | MEDLINE | ID: mdl-27719914

ABSTRACT

Extracts with water:ethanol (100:0, 70:30, 50:50, 30:70, 0:100) solutions from fresh (F), just dried (JD), dried and stored for one year (DS) Justicia spicigera leaves were obtained using the stirring and ultrasound techniques. Extracts were analyzed in physicochemical and antioxidant characteristics. Identification of chemical compounds by gas chromatography-mass spectroscopy (GC-MS) was also performed. 2.14±0.91, 5.67±1.70, and 8.52±4.97g Gallic acid equivalents/100g dry weight (d.w.) of phenolic compounds were found, in average, for F, JD, and DS J. spicigera, respectively. 2.22±1.31, 2.58±2.11, and 8.48±3.78g Trolox equivalents/100g d.w. were detected with the ABTS method and 0.49±0.33, 1.23±0.87, and 0.88±0.94g with the DPPH method for F, JD and DS J. spicigera, respectively. Eucalyptol, phytol, and azulene were identified as the main compounds. J. spicigera showed colors (green-iridescent, green-yellow, or pink of different intensities) and antioxidant characteristics depending on the solvent concentration. Extracts could be used in the food and pharmaceutical industries.


Subject(s)
Antioxidants/analysis , Chemical Phenomena , Justicia/chemistry , Azulenes/analysis , Chromans/analysis , Color , Cyclohexanols/analysis , Eucalyptol , Gallic Acid/analysis , Gas Chromatography-Mass Spectrometry , Monoterpenes/analysis , Phenols/analysis , Phytol/analysis , Plant Extracts/analysis , Plant Extracts/pharmacology , Plant Leaves/chemistry
3.
Nat Prod Res ; 27(9): 841-6, 2013.
Article in English | MEDLINE | ID: mdl-22840199

ABSTRACT

The chemical composition of the Pelargonium graveolens essential oil allowed the identification of 15 compounds (93.86% of the total essential oil). The major fractions were citronellol (35%) and geraniol (28.8%). The chemical composition of the Artemisia arborescens essential oil revealed twenty-one compounds representing 93.57% of the total essential oil. The main compounds were chamazulene (31.9%) and camphor (25.8%). The insecticidal effects were tested towards the insect Rhysopertha dominica. Results revealed that these two essential oils were highly effective against R. dominica at the dose of 50 µL on Petri dish of 8.5 cm of diameter. The antifungal activity was evaluated against Rhizoctonia solani and results showed that both of the essential oils were highly active at a dose of 12.5 µL/20 mL of PDA. Moreover, the inhibitory effect of P. graveolens essential oil was evidenced as stronger than that of the A. arborescens oil for all the tested doses.


Subject(s)
Antifungal Agents/pharmacology , Artemisia/chemistry , Coleoptera/drug effects , Insecticides/pharmacology , Oils, Volatile/chemistry , Oils, Volatile/pharmacology , Pelargonium/chemistry , Rhizoctonia/drug effects , Acyclic Monoterpenes , Animals , Antifungal Agents/chemistry , Azulenes/analysis , Camphor/analysis , Dose-Response Relationship, Drug , Gas Chromatography-Mass Spectrometry , Insecticides/chemistry , Monoterpenes/analysis , Plant Oils/chemistry , Plant Oils/pharmacology , Terpenes/analysis , Tunisia
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