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1.
Food Res Int ; 191: 114735, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39059967

ABSTRACT

The present study was carried out to investigate the proximate composition, fatty acid (FA) profile and volatile compounds (VC) of cooked green licuri (Syagrus coronata) - an unripe stage that is then cooked - and naturally ripe licuri almonds. The FA profiles were determined by gas chromatography (GC) and the VC composition was evaluated using headspace-solid-phase microextraction coupled with GC-MS. The cooked green licuri presented higher moisture, and lower contents of ashes, proteins and lipids than naturally ripe licuri almonds. The FA profiles of cooked green licuri and naturally ripe licuri almonds showed that saturated FAs were predominant (80%) in both samples, and the concentrations of lauric, palmitic, and oleic acids in naturally ripe licuri almonds were higher than those in cooked green licuri. Limonene was the predominant compound in naturally ripe licuri almonds. The main class of VC in the cooked green licuri were aldehydes, with 3-methyl-butanal and furfural being the main species. Alcohols, such as 3-methyl-butanol and 2-heptanol, were the main class of VC in naturally ripe licuri almonds. Among the volatile compounds, 1-hexanol and 2-nonanone contributed to the aroma of cooked green licuri almonds, whereas 2-heptanone, ethanol, and limonene contributed to the aroma of naturally ripe licuri almonds (almonds not subjected to any cooking process). In a word, cooked green licuri and naturally riped licuri almonds, despite having different proximate compositions, present similar fatty acid profile and distinct aromatic characteristics. Therefore, cooked green licuri and naturally riped licuri almonds are an alternative source of nutrient and could be investigated for the use in the food industry to enhance flavor and aroma to new products.


Subject(s)
Cooking , Fatty Acids , Gas Chromatography-Mass Spectrometry , Volatile Organic Compounds , Volatile Organic Compounds/analysis , Fatty Acids/analysis , Brazil , Solid Phase Microextraction , Cyclohexenes/analysis , Terpenes/analysis , Limonene/analysis , Odorants/analysis , Palmitic Acid/analysis , Oleic Acid/analysis , Aldehydes/analysis , Lauric Acids/analysis , Pentanols/analysis
2.
Biomed Chromatogr ; 35(4): e5037, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33238042

ABSTRACT

Perillyl alcohol (POH) is a monocyclic terpene that has strong antitumor activity. Brain tumors are particularly difficult to treat with therapeutic agents, and clinical trials have shown their low tolerance through oral administration. We proposed the entrapment of POH into an oil-in-water chitosan nanoemulsion aiming its intranasal administration for brain targeting. An ultra-performance liquid chromatography/tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for the quantitation of total metabolite perillic acid (PA) in plasma and brain of rats. The rat samples containing the metabolite were treated by liquid-liquid extraction with acetonitrile. The mobile phase was 0.1% formic acid in water (solvent A) and 0.1% formic acid in methanol (solvent B), at a flow rate of 0.3 mL min-1 in gradient elution. The chromatography was run for 10 min, and analytical curves were built in acetonitrile, plasma, and brain. The PA was detected in positive ion mode with multiple reaction monitoring. The method has shown high selectivity, sensitivity, and throughput. The low quantification limits of 162, 178, and 121 ng mL-1 for acetonitrile, brain, and plasma, respectively, indicate a good detectability of the method. The repeatability and precision observed were within the limits recommended in the literature. The accuracy of the method was verified through high recovery rates (106-118%). The validated method was successfully applied to the pharmacokinetic study of the metabolite PA after the intranasal administration of free or POH-loaded nanoemulsion in rats. The results showed that chitosan nanoemulsion improved the plasma and brain bioavailability of POH, representing a promising alternative to free POH treatment.


Subject(s)
Brain Chemistry/drug effects , Chromatography, High Pressure Liquid/methods , Cyclohexenes , Emulsions , Monoterpenes , Administration, Intranasal , Animals , Cyclohexenes/analysis , Cyclohexenes/blood , Cyclohexenes/pharmacokinetics , Emulsions/administration & dosage , Emulsions/chemistry , Emulsions/pharmacokinetics , Limit of Detection , Linear Models , Monoterpenes/administration & dosage , Monoterpenes/analysis , Monoterpenes/blood , Monoterpenes/chemistry , Monoterpenes/pharmacokinetics , Nanostructures/administration & dosage , Rats , Reproducibility of Results , Tandem Mass Spectrometry/methods
3.
Molecules ; 24(8)2019 Apr 25.
Article in English | MEDLINE | ID: mdl-31027274

ABSTRACT

The chemical composition and biological activity of essential oils isolated from the leaves of Siparuna aspera, Siparuna macrotepala, Piper leticianum, Piper augustum and the rhizome of Hedychium coronarium were evaluated. These species are used medicinally in different ways by the Amazonian communities that live near the Kutukú mountain range. Chemical studies revealed that the main components for the two Siparuna species were germacrene D, bicyclogermacrene, α-pinene, δ-cadinene, δ-elemene, α-copaene and ß-caryophyllene; for the two Piper species ß-caryophyllene, germacrene D, α-(E,E)-farnesene, ß-elemene, bicyclogermacrene, δ-cadinene and for H. coronarium 1,8-cineole, ß-pinene, α-pinene and α-terpineol. The antioxidant activity of all essential oils was evaluated by 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS), photochemiluminescence (PCL) quantitative assays, and DPPH and ABTS bioautographic profiles, with different results for each of them. Antimicrobial activity studies were carried out on three yeasts, six Gram positive and four Gram negative bacteria, by means of the disc diffusion method. The essential oil of H. coronarium showed the most relevant results on L. grayi, K. oxytoca and S. mutans, P. augustum and P. leticianum on S. mutans. An antibacterial bioautographic test for H. coronarium was also carried out and highlighted the potential activity of terpinen-4-ol and 1,8-cineole.


Subject(s)
Oils, Volatile/analysis , Zingiberaceae/chemistry , Anti-Bacterial Agents/analysis , Anti-Bacterial Agents/pharmacology , Bicyclic Monoterpenes , Bridged Bicyclo Compounds/analysis , Bridged Bicyclo Compounds/pharmacology , Cyclohexane Monoterpenes , Cyclohexenes/analysis , Cyclohexenes/pharmacology , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Microbial Sensitivity Tests , Monoterpenes/analysis , Monoterpenes/pharmacology , Oils, Volatile/pharmacology , Rainforest , Sesquiterpenes/analysis , Sesquiterpenes/pharmacology
4.
J Sci Food Agric ; 98(9): 3409-3415, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29280145

ABSTRACT

BACKGROUND: Propolis is a complex mixture that honey bees produce from the exudates of various plants and presents many medicinal properties. Its chemical composition varies according to the phytogeography characteristics of each region, among others. The aim of this study was to identify and characterize the volatile organic compounds (VOCs) present in Venezuelan propolis and compare with reference samples such as Brazilian and Argentinian propolis. RESULTS: A total of 90 VOCs were identified in a series of propolis samples using both solid-phase microextraction and dynamic headspace (DHS), both coupled to a gas chromatograph-electron ionization mass spectrometer. In the case of Venezuelan propolis, sesquiterpenes, esters, aromatic compounds, and aliphatic hydrocarbons were identified. Limonene was found only in Venezuelan samples, this being the first time it has been identified in samples from this country. In the case of green propolis, ß-caryophyllene and nerolidol were the major compounds. As for the Argentinian samples, prenyl acetate, benzyl acetate, and 2-phenylethyl acetate were detected only in these samples. CONCLUSIONS: Possible chemical markers of natural sources such as limonene were detected using DHS extraction. Several compounds have also been identified for the first time in Venezuelan propolis. Cluster analysis allowed the relating of the propolis VOCs profile to their provenance. © 2017 Society of Chemical Industry.


Subject(s)
Propolis/chemistry , Volatile Organic Compounds/analysis , Animals , Argentina , Bees , Brazil , Cyclohexenes/analysis , Gas Chromatography-Mass Spectrometry/methods , Limonene , Sesquiterpenes/analysis , Solid Phase Microextraction , Spectrometry, Mass, Electrospray Ionization/methods , Terpenes/analysis , Venezuela
5.
An Acad Bras Cienc ; 88(3 Suppl): 1899-1907, 2016.
Article in English | MEDLINE | ID: mdl-27901194

ABSTRACT

Aldama arenaria and A. robusta are morphologically similar aromatic species that have seasonal development. The yield and chemical composition of essential oils from aerial and underground vegetative organs of these species were compared to verify the production of volatile metabolites in flowering and dormant phases of development and to identify if there are unique compounds for either species. The major compound in the essential oils from A. arenaria leaves was palustrol (16.22%) and for aerial stems was limonene (15.3%), whereas limonene (11.16%) and α-pinene (19.64%) were the major compounds for leaves and aerial stems from A. robusta, respectively. The major compound for the underground organs was α-pinene, in both species and phenological stages. High amounts of diterpenes were found especially for A. arenaria essential oils. Each analyzed species presented unique compounds, which can provide a characteristic chemical profile for both species helping to solve their taxonomic problems. This study characterized for the first time the yield and essential oil composition of A. arenaria and A. robusta, which have medicinal potential, and some of the compounds in their essential oils are unique to each one and may be useful in helping the correct identification of them.


Subject(s)
Asteraceae/chemistry , Oils, Volatile/chemistry , Plant Oils/chemistry , Seasons , Bicyclic Monoterpenes , Brazil , Cyclohexenes/analysis , Gas Chromatography-Mass Spectrometry , Limonene , Monoterpenes/analysis , Plant Leaves/chemistry , Plant Roots/chemistry , Plant Stems/chemistry , Terpenes/analysis
6.
Exp Parasitol ; 165: 64-70, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26993082

ABSTRACT

Essential oil from fresh leaves of the shrub Piper corcovadensis (Miq.) C. DC was obtained in 0.21% (w/w) yield by hydrodistillation in a Clevenger type apparatus. Thirty-one components, accounting for 96.61% of the leaf oil, were identified by gas chromatography-mass spectrometry. The major constituents of the oil were 1-butyl-3,4-methylenedioxybenzene (30.62%), terpinolene (17.44%), trans -caryophyllene (6.27%), α-pinene (5.92%), δ-cadinene (4.92%), and Limonene (4.46%). Bioassays against larvae of the Dengue mosquito (Aedes aegypti) revealed that leaf oil (LC50 = 30.52 ppm), terpinolene (LC50 = 31.16 ppm), and pure 1-butyl-3,4-methylenedioxybenzene (LC50 = 22.1 ppm) possessed larvicidal activities and are able to interfere with the activity of proteases from L4 gut enzymes. Additionally, the essential oil exhibited a strong oviposition deterrent activity at 50 and 5 ppm. This paper constitutes the first report of biological activities associated with the essential oil of leaves of P. corcovadensis.


Subject(s)
Aedes , Mosquito Vectors , Oils, Volatile/chemistry , Piper/chemistry , Aedes/drug effects , Aedes/physiology , Animals , Bicyclic Monoterpenes , Biological Assay , Cyclohexane Monoterpenes , Cyclohexenes/analysis , Dengue/transmission , Electrophoresis, Polyacrylamide Gel , Gas Chromatography-Mass Spectrometry , Larva/enzymology , Limonene , Monoterpenes/analysis , Mosquito Vectors/drug effects , Mosquito Vectors/physiology , Oils, Volatile/isolation & purification , Oils, Volatile/pharmacology , Oviposition/drug effects , Peptide Hydrolases/analysis , Plant Leaves/chemistry , Polycyclic Sesquiterpenes , Protease Inhibitors/pharmacology , Sesquiterpenes/analysis , Terpenes/analysis , Trypsin/drug effects , Trypsin/metabolism
7.
J Sep Sci ; 38(17): 3038-46, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26140379

ABSTRACT

The Baccharis genus has more than 400 species of aromatic plants. However, only approximately 50 species have been studied in oil composition to date. From these studies, very few take into consideration differences between male and female plants, which is a significant and distinctive factor in Baccharis in the Asteraceae family. Baccharis articulata is a common shrub that grows wild in south Brazil, northern and central Argentina, Bolivia, Paraguay and Uruguay. It is considered to be a medicinal plant and is employed in traditional medicine. We report B. articulata male and female volatile composition obtained by simultaneous distillation-extraction technique and analyzed by gas chromatography with mass spectrometry. Also, an assessment of aromatic differences between volatile extracts was evaluated by gas chromatography with olfactometry. The results show a very similar chemical composition between male and female extracts, with a high proportion of terpene compounds of which ß-pinene, limonene and germacrene D are the main components. Despite the chemical similarity, great differences in aromatic profile were found: male plant samples exhibited the strongest odorants in number and intensity of aromatic attributes. These differences explain field observations which indicate differences between male and female flower aroma, and might be of ecological significance in the attraction of pollinating insects.


Subject(s)
Baccharis/chemistry , Gas Chromatography-Mass Spectrometry/methods , Olfactometry/methods , Plant Extracts/analysis , Baccharis/physiology , Bicyclic Monoterpenes , Bridged Bicyclo Compounds/analysis , Chromatography, Thin Layer , Cyclohexenes/analysis , Distillation , Limonene , Monoterpenes/analysis , Odorants/analysis , Oils, Volatile/analysis , Plants, Medicinal/chemistry , Plants, Medicinal/physiology , Sesquiterpenes, Germacrane/analysis , Temperature , Terpenes/analysis , Volatile Organic Compounds/analysis
8.
Chem Biodivers ; 12(4): 652-61, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25879508

ABSTRACT

Climate change, unseasonal fire and urbanization are contributing to the decline of Pinus caribaea var. bahamensis populations in the Turks and Caicos Islands (TCI). Infestation of pines with the invasive pine tortoise scale (PTS, Toumeyella parvicornis) is accelerating this decline. Pine trees in the Bahamas are larger and healthier and are not infested with PTS although they are subject to some of the same environmental pressures as the trees in TCI. Volatile compounds were collected from wild and nursery-reared P. caribaea var. bahamensis from TCI and the Bahamas and characterized using GC/MS analysis, to look for differences between the compounds detected in insect-infested pines of TCI and the healthy pines of the Bahamas. Ten compounds contributing at least 1% of the total detected peak areas in any one of the samples were selected for further study. Eight of these compounds were identified using authentic standards and mass spectral libraries. The main constituents in the samples were α- and ß-pinene as well as ß-phellandrene, and, together with ß-myrcene, their contents varied the most between samples collected at different locations. Principal-component analysis showed that the two structural isomers of pinene, together with ß-myrcene and ß-phellandrene, contributed 98.4% of the variance between samples. There was a positive relationship between the concentrations of the two structural isomers of pinene and between levels of ß-myrcene and ß-phellandrene. The results are discussed in relation to the biology and adaptations of invasive scale insects, the importance of monoterpenes in pine as a defense against insect predation, whether these compounds can be used as indicators of tree health, and future directions for research into conserving the Caicos pine.


Subject(s)
Hemiptera , Herbivory , Pinus/chemistry , Pinus/physiology , Volatile Organic Compounds/chemistry , Acyclic Monoterpenes , Adaptation, Physiological , Animals , Bahamas , Bicyclic Monoterpenes , Bridged Bicyclo Compounds/analysis , Cyclohexane Monoterpenes , Cyclohexenes/analysis , Gas Chromatography-Mass Spectrometry , Hemiptera/physiology , Introduced Species , Monoterpenes/analysis , Principal Component Analysis , Volatile Organic Compounds/analysis , West Indies
9.
Nat Prod Res ; 29(7): 667-70, 2015.
Article in English | MEDLINE | ID: mdl-25421822

ABSTRACT

The species Myrocarpus frondosus is native to southern Brazil, and it is known as cabreúva. It is a large tree, and its wood is used as a reservoir for distilled spirits, especially Cachaça. In this pioneering work, the essential oil was extracted monthly from the leaves of M. frondosus, for a period of 1 year. The essential oil was extracted by using hydrodistillation and the determination of the chemical composition of essential oil was performed by using the chromatographic techniques GC-FID and GC-MS. Thirty-three compounds were identified in the essential oil and bicyclogermacrene was the major compound. Through multivariate analysis, it was determined that ß-caryophyllene, limonene and terpinen-4-ol were directly proportional to climatic factors. The yield of the oil was directly proportional to temperature and radiation.


Subject(s)
Climate , Fabaceae/chemistry , Oils, Volatile/chemistry , Plant Leaves/chemistry , Plant Oils/chemistry , Brazil , Cyclohexenes/analysis , Gas Chromatography-Mass Spectrometry , Limonene , Polycyclic Sesquiterpenes , Seasons , Sesquiterpenes/analysis , Sesquiterpenes, Germacrane/analysis , Terpenes/analysis
10.
Nat Prod Commun ; 8(10): 1477-8, 2013 Oct.
Article in English | MEDLINE | ID: mdl-24354206

ABSTRACT

The volatile components from the leaves of Erechtites valerianaefolia (Wolf) DC. were obtained by hydrodistillation and analyzed by GC/MS. A total of 12 compounds, representing 99.8% of the oil, were identified. The dominant compounds were limonene (56.7%), myrcene (12.7%), trans-beta-farnesene (10.2%) and l-phellandrene (8.7%).


Subject(s)
Asteraceae/chemistry , Oils, Volatile/chemistry , Cyclohexenes/analysis , Limonene , Terpenes/analysis , Venezuela
11.
Planta Med ; 79(14): 1307-12, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23945759

ABSTRACT

This study aimed to determine the composition of the essential oil of Mentha x villosa and to evaluate its biological effects in vitro on adult worms of S. mansoni. Rotundifolone (70.96 %), limonene (8.75 %), trans-caryophyllene (1.46 %), and ß-pinene (0.81 %) were shown to be the major constituents of this oil. Adult worms of S. mansoni were incubated with different concentrations of the essential oil (1, 10, 100, 250, 500, and 1000 µg/mL) and of its constituents rotundifolone (0.7, 3.54, 7.09, 70.96, 177.4, 354.8, and 700.96 µg/mL), limonene (43.75 µg/mL), trans-caryophyllene (7.3 µg/mL), and ß-pinene (4.03 µg/mL). No schistosomicidal activity was identified at the trans-caryophyllene and ß-pinene concentrations studied. However, use of the essential oil (10 µg/mL), rotundifolone (7.09 µg/mL), and limonene (43.75 µg/mL) resulted in decreased worm motility continuing until 96 hours of observation. At higher concentrations (100 and 70.96 µg/mL, respectively), both the essential oil and rotundifolone caused mortality among adult worms of S. mansoni. The positive control praziquantel caused the death of all parasites after 24 h of evaluation. The results from this study suggest that the essential oil of Mentha x villosa presents schistosomicidal efficacy.


Subject(s)
Mentha/chemistry , Oils, Volatile/pharmacology , Plant Extracts/pharmacology , Schistosoma mansoni/drug effects , Schistosomicides/pharmacology , Animals , Bicyclic Monoterpenes , Bridged Bicyclo Compounds/analysis , Bridged Bicyclo Compounds/pharmacology , Cyclohexenes/analysis , Cyclohexenes/pharmacology , Limonene , Monoterpenes/analysis , Monoterpenes/pharmacology , Oils, Volatile/chemistry , Plant Extracts/chemistry , Polycyclic Sesquiterpenes , Sesquiterpenes/analysis , Sesquiterpenes/pharmacology , Terpenes/analysis , Terpenes/pharmacology
12.
J Food Sci ; 76(7): C997-1002, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21819399

ABSTRACT

UNLABELLED: For the first time, the production of an extracellular ß-glucosidase (Sp-ß-gl) by a Sporidiobolus pararoseus yeast strain is reported. The Sp-ß-gl activity was quantified, characterized, and assessed for its efficiency in releasing aroma-enhancing compounds in wines. The maximum enzymatic synthesis was after 72 h of growth in a complex media with 20 g/L of cellobiose. The optimal pH and temperature were 5.5 and at 50 °C, respectively. It showed a wide range of pH stability and exhibited quite high thermostability at low temperatures. In addition, this ß-glucosidase revealed tolerance to wine-associated inhibitory compounds (sugars and ethanol), showing suitable characteristics for all the stages of alcoholic fermentation. The hydrolysis of the glycosidic terpenes by Sp-ß-gl was studied by gas chromatography, and its ability to efficiently release free terpenols has been demonstrated. The concentrations of geraniol, linalool, α-terpineol, and nerol were significantly increased in treated wines. These results suggest the potential application of this new yeast ß-glucosidase as an aroma-enhancing enzyme in winemaking. PRACTICAL APPLICATION: The search for new ß-glucosidase from yeast sources is important to improve the quality of wines. In this work, an S. pararoseus yeast strain has shown to be capable to produce a ß-glucosidase with suitable combination of properties for functionality in wines and with potential to increase the concentration of free aroma compounds, showing good prospects for an industrial application.


Subject(s)
Basidiomycota/enzymology , Food Handling/methods , Wine , beta-Glucosidase/metabolism , Acyclic Monoterpenes , Cyclohexane Monoterpenes , Cyclohexenes/analysis , Enzyme Stability , Fermentation , Hydrogen-Ion Concentration , Monoterpenes/analysis , Odorants/analysis , Temperature , Terpenes/analysis , Terpenes/metabolism
13.
J Chem Ecol ; 37(6): 565-74, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21559877

ABSTRACT

The tomato leafminer Tuta absoluta (Lepidoptera: Gelechiidae) is a devastating pest of cultivated tomato Solanum lycopersicum throughout South and Central America and Europe. We aimed to characterize the behavioral mechanisms and the chemical cues involved in host selection of T. absoluta females by chemical analysis of tomato leaf volatiles, wind tunnel attraction assays, and oviposition bioassays. Tomato leaf odor elicited in mated females upwind orientation flight followed by landing as well as egg-laying, demonstrating the essential role of plant volatiles in T. absoluta host-finding behavior. In wind tunnel and oviposition choice experiments, T. absoluta females significantly preferred tomato S. lycopersicum over wild tomato Solanum habrochaites, which is resistant to larval feeding. This indicates that leaf volatiles provide information on the suitability of plants as larval hosts. Mated females also discriminated three cultivars of S. lycopersicum according to their volatile profiles. Headspace collections from leaves of these three cultivars contained large amounts of ß-phellandrene, followed by limonene, 2-carene, and (E)-ß-caryophyllene, which together accounted for more than 70% of tomato foliage headspace. Most leaf volatiles were released by all three cultivars, but they showed significant differences with respect to the presence of a few minor compounds and blend proportion. This is an initial study of the volatile signatures that mediate attraction and oviposition of tomato leafminer T. absoluta in response to its main host, tomato.


Subject(s)
Behavior, Animal/drug effects , Moths/physiology , Solanum lycopersicum/chemistry , Volatile Organic Compounds/pharmacology , Animals , Brazil , Cues , Cyclohexenes/analysis , Cyclohexenes/pharmacology , Female , Moths/drug effects , Odorants , Oviposition , Plant Leaves/chemistry , Terpenes/analysis , Terpenes/pharmacology , Volatile Organic Compounds/chemistry
14.
Nat Prod Commun ; 6(11): 1711-4, 2011 Nov.
Article in English | MEDLINE | ID: mdl-22224294

ABSTRACT

Lemon verbena (Aloysia citriodora Palau) is indigenous to South America and was introduced into Europe. It is cultivated mainly due to the lemon-like aroma emitted from its leaves, which are utilized for the preparation of herbal tea reputed to have antispasmodic, antipyretic, sedative and digestive properties. In this work we introduce the enantiomeric distribution of sabinene and limonene by bidimensional gas chromatography (chiral GC-GC) as a genuine quantitative parameter in order to improve the knowledge so far available on A. citriodora oil. Multivariate analysis afforded information on the similarities and differences of wild and cultivated A. citriodora populations during different seasons in the same environmental conditions. The results indicated that it was possible to discard the environmental and seasonal effect on the chemical composition of A. citriodora for wild and cultivated materials belonging to the same genetic origin.


Subject(s)
Cyclohexenes/analysis , Environment , Monoterpenes/analysis , Oils, Volatile/chemistry , Terpenes/analysis , Verbenaceae/chemistry , Argentina , Bicyclic Monoterpenes , Cyclohexenes/chemistry , Limonene , Monoterpenes/chemistry , Seasons , Stereoisomerism , Terpenes/chemistry
15.
Rev Cubana Med Trop ; 59(2): 154-8, 2007.
Article in Spanish | MEDLINE | ID: mdl-23427450

ABSTRACT

Gas chromatography test and Gas chromatography/mass spectrometry test allowed examining the essential oil from Pimenta racemosa leaves (Mill.) J.W. Moore (Myrtales: Myrtaceae). A total of 26 volatile compounds representing 99.5% of the whole composition were identified, being ternipen 4-ol and 1.8 cineol those having the largest portions. Lab bioassays were performed with 5 different oil doses on Blattella germanica. DL50, 15.55 and DL95 = 48.16% were estimated by a probit-log analysis as well as diagnostic dose of 2 microg/insect of 50% oil that is recommended for field surveillance of the use of various formulations in insect control programs.


Subject(s)
Blattellidae , Insecticides/analysis , Oils, Volatile/analysis , Pimenta/chemistry , Plant Oils/analysis , Administration, Topical , Allylbenzene Derivatives , Animals , Anisoles/analysis , Cyclohexane Monoterpenes , Cyclohexanols/analysis , Cyclohexenes/analysis , Eucalyptol , Eugenol/analysis , Gas Chromatography-Mass Spectrometry , Insecticides/administration & dosage , Lethal Dose 50 , Male , Monoterpenes/analysis , Oils, Volatile/administration & dosage , Oils, Volatile/isolation & purification , Plant Leaves/chemistry , Plant Oils/administration & dosage , Plant Oils/isolation & purification , Terpenes/analysis
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