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Registro Completo |
Biblioteca(s): |
Embrapa Agroenergia; Embrapa Algodão. |
Data corrente: |
29/09/2015 |
Data da última atualização: |
15/03/2016 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
BARROS, T. F. S.; ARRIEL, N. H. C.; QUEIROZ, M. F.; FERNANDES, P. D.; MENDONCA, S.; RIBEIRO, J. A. de A.; MEDEIROS, E. de A. |
Afiliação: |
Talita Farias Sousa Barros, UNIVERSIDADE DA PARAÍBA; Nair Helena Castro Arriel, EMBRAPA ALGODÃO; Messias Firmino Queiroz, UNIVERSIDADE DA PARAÍBA; Pedro Dantas Fernandes, UNIVERSIDADE DA PARAÍBA; SIMONE MENDONCA, CNPAE; JOSE ANTONIO DE AQUINO RIBEIRO, CNPAE; Everaldo Paulo Medeiros, EMBRAPA ALGODÃO. |
Título: |
Fatty acid profiles of species of Jatropha curcas L., Jatropha molíssima (Pohl) Baill. and Jatropha gossypiifolia L. |
Ano de publicação: |
2015 |
Fonte/Imprenta: |
Industrial Crops and Products, v. 73, p. 106-108, 2015. |
Idioma: |
Inglês |
Conteúdo: |
The purpose of this study was to determine a standard of fatty acids from species of Jatropha curcas L., Jatropha mollissima (Pohl) Baill., and Jatropha gossypiifolia L. The sample set consisted of 11 samples with three repetitions for each species, resulting in a total of 99 samples. Matrix of fatty acid data, principal component analyses (PCA) techniques and hierarchical cluster analyses (HCA) were applied in order to verify the similarity and discrimination of the samples for fatty acid profile. The PC1 (x-axis) discriminates against samples of J. curcas, J. mollissima and J. gossypiifolia while these latter two species are discriminated in PC2 (y-axis). In the HCA, the dendrogram also shows the separation of the three species as was observed during the PCA. The major variations in this separation were oleic (C18:1), linoleic (C18:2), stearic (C18:0) and palmitic (C16:0) acids. In both J. mollissima and J. gossypiifolia there is a predominance of linoleic acid (C18:2), whereas for J. curcas there is a balance on the equivalent proportion of oleic (C18:1) and linoleic (C18:2) acids. Oleic (C18:1) and linoleic (C18:2) acids sum constitute a mean of 76.5%, 78.5%, 84.5% of the total sample composition of J. curcas, J. mollissima and J. gossypiifolia, respectively. For the studied species of Jatropha, the mean oil content was 35.0% for J. curcas, 18.3% for J. mollissima and 22.1 % for J. gossypiifolia. The difference between the oil content in the species comes from the proportion of fatty acids in the lipid composition, especially for oleic (C18:1) and linoleic (C18:2) acids. Overlapping similarities and differences in lipid composition did allow differentiation between species studied. MenosThe purpose of this study was to determine a standard of fatty acids from species of Jatropha curcas L., Jatropha mollissima (Pohl) Baill., and Jatropha gossypiifolia L. The sample set consisted of 11 samples with three repetitions for each species, resulting in a total of 99 samples. Matrix of fatty acid data, principal component analyses (PCA) techniques and hierarchical cluster analyses (HCA) were applied in order to verify the similarity and discrimination of the samples for fatty acid profile. The PC1 (x-axis) discriminates against samples of J. curcas, J. mollissima and J. gossypiifolia while these latter two species are discriminated in PC2 (y-axis). In the HCA, the dendrogram also shows the separation of the three species as was observed during the PCA. The major variations in this separation were oleic (C18:1), linoleic (C18:2), stearic (C18:0) and palmitic (C16:0) acids. In both J. mollissima and J. gossypiifolia there is a predominance of linoleic acid (C18:2), whereas for J. curcas there is a balance on the equivalent proportion of oleic (C18:1) and linoleic (C18:2) acids. Oleic (C18:1) and linoleic (C18:2) acids sum constitute a mean of 76.5%, 78.5%, 84.5% of the total sample composition of J. curcas, J. mollissima and J. gossypiifolia, respectively. For the studied species of Jatropha, the mean oil content was 35.0% for J. curcas, 18.3% for J. mollissima and 22.1 % for J. gossypiifolia. The difference between the oil content in the species comes from the propor... Mostrar Tudo |
Palavras-Chave: |
Analise de agrupamentos hierárquicos; Análises dos componentes principais; Cromatografia em fase gasosa; Gas chrom atography; Hierarchical clusters analyses; Principal component analyses. |
Thesagro: |
Jatropha curcas. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/141191/1/Fatty-acid-profiles-of-species-of-Jatropha-curcas-L.....pdf
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Marc: |
LEADER 02646naa a2200277 a 4500 001 2041000 005 2016-03-15 008 2015 bl uuuu u00u1 u #d 100 1 $aBARROS, T. F. S. 245 $aFatty acid profiles of species of Jatropha curcas L., Jatropha molíssima (Pohl) Baill. and Jatropha gossypiifolia L.$h[electronic resource] 260 $c2015 520 $aThe purpose of this study was to determine a standard of fatty acids from species of Jatropha curcas L., Jatropha mollissima (Pohl) Baill., and Jatropha gossypiifolia L. The sample set consisted of 11 samples with three repetitions for each species, resulting in a total of 99 samples. Matrix of fatty acid data, principal component analyses (PCA) techniques and hierarchical cluster analyses (HCA) were applied in order to verify the similarity and discrimination of the samples for fatty acid profile. The PC1 (x-axis) discriminates against samples of J. curcas, J. mollissima and J. gossypiifolia while these latter two species are discriminated in PC2 (y-axis). In the HCA, the dendrogram also shows the separation of the three species as was observed during the PCA. The major variations in this separation were oleic (C18:1), linoleic (C18:2), stearic (C18:0) and palmitic (C16:0) acids. In both J. mollissima and J. gossypiifolia there is a predominance of linoleic acid (C18:2), whereas for J. curcas there is a balance on the equivalent proportion of oleic (C18:1) and linoleic (C18:2) acids. Oleic (C18:1) and linoleic (C18:2) acids sum constitute a mean of 76.5%, 78.5%, 84.5% of the total sample composition of J. curcas, J. mollissima and J. gossypiifolia, respectively. For the studied species of Jatropha, the mean oil content was 35.0% for J. curcas, 18.3% for J. mollissima and 22.1 % for J. gossypiifolia. The difference between the oil content in the species comes from the proportion of fatty acids in the lipid composition, especially for oleic (C18:1) and linoleic (C18:2) acids. Overlapping similarities and differences in lipid composition did allow differentiation between species studied. 650 $aJatropha curcas 653 $aAnalise de agrupamentos hierárquicos 653 $aAnálises dos componentes principais 653 $aCromatografia em fase gasosa 653 $aGas chrom atography 653 $aHierarchical clusters analyses 653 $aPrincipal component analyses 700 1 $aARRIEL, N. H. C. 700 1 $aQUEIROZ, M. F. 700 1 $aFERNANDES, P. D. 700 1 $aMENDONCA, S. 700 1 $aRIBEIRO, J. A. de A. 700 1 $aMEDEIROS, E. de A. 773 $tIndustrial Crops and Products$gv. 73, p. 106-108, 2015.
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Registro original: |
Embrapa Algodão (CNPA) |
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Registro Completo
Biblioteca(s): |
Embrapa Agroindústria de Alimentos. |
Data corrente: |
10/10/2017 |
Data da última atualização: |
10/10/2017 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
SILVA, E. R. DA; BIZZO, H. R.; FERNANDES, P. D.; VEIGA JUNIOR, V. F. DA; LEITÃO, S. G.; OLIVEIRA, D. R. DE. |
Afiliação: |
EDUARDO R. DA SILVA, UFRJ; HUMBERTO RIBEIRO BIZZO, CTAA; PATRÍCIA D. FERNANDES, UFRJ; VALDIR F. DA VEIGA JUNIOR, UFA; SUZANA G. LEITÃO, UFRJ; DANILO R. DE OLIVEIRA, UFRJ. |
Título: |
Development and evaluation of an inhalation chamber for in vivo tests. |
Ano de publicação: |
2017 |
Fonte/Imprenta: |
Anais da Academia Brasileira de Ciências, v. 89, n. 3, p. 1643-1653, 2017. |
Idioma: |
Inglês |
Conteúdo: |
The bioavailability, toxicity, and therapeutic efficacy of a drug is directly related to its administration route. The pulmonary route can be accessed by inhalation after fumigation, vaporization or nebulization. Thus, pharmacological and toxicological evaluation accessed by an apparatus specifically designed and validated for this type of administration is extremely important. Based on pre-existing models, an inhalation chamber was developed. This presents a central structure with five animal holders. The nebulized air passes directly and continuously through these holders and subsequently to an outlet. Evaluation of its operation was performed using clove essential oil, a nebulizer, and a flow meter. The air within the chamber was collected by static headspace and analyzed by gas chromatography with a flame ionization detector. For this purpose, a 2.5 minutes chromatographic method was developed. The air flow in each of the five outputs was 0.92 liters per minute. During the first minute, the chamber became saturated with the nebulized material. Homogeneous and continuous operation of the chamber was observed without accumulation of volatile material inside it for 25 minutes. The inhalation chamber works satisfactorily for in vivo tests with medicines designed to be administrated by inhalation. |
Palavras-Chave: |
Biological activities; Gas chromatograph; Headspace; Inhalation chamber. |
Thesagro: |
Syzygium Aromaticum. |
Thesaurus NAL: |
Gas chromatography; Headspace analysis. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
Marc: |
LEADER 02117naa a2200265 a 4500 001 2077098 005 2017-10-10 008 2017 bl uuuu u00u1 u #d 100 1 $aSILVA, E. R. DA 245 $aDevelopment and evaluation of an inhalation chamber for in vivo tests.$h[electronic resource] 260 $c2017 520 $aThe bioavailability, toxicity, and therapeutic efficacy of a drug is directly related to its administration route. The pulmonary route can be accessed by inhalation after fumigation, vaporization or nebulization. Thus, pharmacological and toxicological evaluation accessed by an apparatus specifically designed and validated for this type of administration is extremely important. Based on pre-existing models, an inhalation chamber was developed. This presents a central structure with five animal holders. The nebulized air passes directly and continuously through these holders and subsequently to an outlet. Evaluation of its operation was performed using clove essential oil, a nebulizer, and a flow meter. The air within the chamber was collected by static headspace and analyzed by gas chromatography with a flame ionization detector. For this purpose, a 2.5 minutes chromatographic method was developed. The air flow in each of the five outputs was 0.92 liters per minute. During the first minute, the chamber became saturated with the nebulized material. Homogeneous and continuous operation of the chamber was observed without accumulation of volatile material inside it for 25 minutes. The inhalation chamber works satisfactorily for in vivo tests with medicines designed to be administrated by inhalation. 650 $aGas chromatography 650 $aHeadspace analysis 650 $aSyzygium Aromaticum 653 $aBiological activities 653 $aGas chromatograph 653 $aHeadspace 653 $aInhalation chamber 700 1 $aBIZZO, H. R. 700 1 $aFERNANDES, P. D. 700 1 $aVEIGA JUNIOR, V. F. DA 700 1 $aLEITÃO, S. G. 700 1 $aOLIVEIRA, D. R. DE 773 $tAnais da Academia Brasileira de Ciências$gv. 89, n. 3, p. 1643-1653, 2017.
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Embrapa Agroindústria de Alimentos (CTAA) |
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