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Registro Completo |
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Biblioteca(s): |
Embrapa Solos. |
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Data corrente: |
16/04/2010 |
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Data da última atualização: |
29/05/2017 |
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Tipo da produção científica: |
Artigo de Divulgação na Mídia |
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Autoria: |
HARTEMINK, A. E.; McBRATNEY, A. B.; HEMPEL, J.; MENDONÇA-SANTOS, M. de L.; McKENZIE, N.; SANCHEZ, P.; GAN-LIN, Z.; MONTANARELLA, L. |
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Afiliação: |
ISRIC - World Soil Information; The University of Sydney, Sydney, Australia; Jon Hempel, National Geospatial Development Center; MARIA DE LOURDES M SANTOS BREFIN, CNPS; Neil McKenzie, CSIRO Land & Water; Pedro Sanchez, CIAT-TSBF; Gan-Lin Zhang, Institute of Soil Science, Chinese Academy of Sciences; Luca Montanarella, European Commission - DG JRC. |
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Título: |
GlobalSoilMap.net: a new digital soil map of the world. |
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Ano de publicação: |
2009 |
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Fonte/Imprenta: |
MEA Bulletin, n. 71, jun. 2009. |
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Páginas: |
2 p. |
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Idioma: |
Inglês |
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Conteúdo: |
Knowledge of the world soil resources is fragmented and dated. There is a need for accurate, up-to-date and spatially referenced soil information as frequently expressed by the modelling community, farmers and land users, and policy and decision makers. This need coincides with an enormous leap in technologies that allow for accurately collecting and predicting soil properties. We are working on a new digital soil map of the world using state-of-the-art and emerging technologies for soil mapping and predicting soil properties. Our aim is to map the global land surface in 5 years ? the resulting maps will depict the primary functional soil properties at a grid resolution of 90×90 m. They will be freely available, web-accessible and widely distributed and used.The maps will be produced by a global consortium with centres in each of the continents: NRCS for North America, Embrapa for Latin America, JRC for Europe, TSBF-CIAT for Africa, ISSAS for parts of Asia and CSIRO for Oceania. This new global soil map will be supplemented by interpretation and functionality options that aim to assist better decisions in a range of global issues like food production and hunger eradication, climate change, and environmental degradation. In November 2008, a grant of US$18 million was obtained from the Bill & Melinda Gates Foundation to map most parts of Sub-Saharan Africa and make the underlying data available. From this grant there are funds for coordinating efforts in the global consortium. |
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Palavras-Chave: |
Digital soil mapping; Mapeamento digital. |
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Categoria do assunto: |
P Recursos Naturais, Ciências Ambientais e da Terra |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/66584/1/GlobalSoilMap.net-A-New-Digital-Soil-Map-of-the-World-Guest-Article-MEA-Bulletin-Issue-No.pdf
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Marc: |
LEADER 02135nam a2200229 a 4500
001 1696753
005 2017-05-29
008 2009 bl uuuu u00u1 u #d
100 1 $aHARTEMINK, A. E.
245 $aGlobalSoilMap.net$ba new digital soil map of the world.$h[electronic resource]
260 $aMEA Bulletin, n. 71, jun. 2009.$c2009
300 $a2 p.
520 $aKnowledge of the world soil resources is fragmented and dated. There is a need for accurate, up-to-date and spatially referenced soil information as frequently expressed by the modelling community, farmers and land users, and policy and decision makers. This need coincides with an enormous leap in technologies that allow for accurately collecting and predicting soil properties. We are working on a new digital soil map of the world using state-of-the-art and emerging technologies for soil mapping and predicting soil properties. Our aim is to map the global land surface in 5 years ? the resulting maps will depict the primary functional soil properties at a grid resolution of 90×90 m. They will be freely available, web-accessible and widely distributed and used.The maps will be produced by a global consortium with centres in each of the continents: NRCS for North America, Embrapa for Latin America, JRC for Europe, TSBF-CIAT for Africa, ISSAS for parts of Asia and CSIRO for Oceania. This new global soil map will be supplemented by interpretation and functionality options that aim to assist better decisions in a range of global issues like food production and hunger eradication, climate change, and environmental degradation. In November 2008, a grant of US$18 million was obtained from the Bill & Melinda Gates Foundation to map most parts of Sub-Saharan Africa and make the underlying data available. From this grant there are funds for coordinating efforts in the global consortium.
653 $aDigital soil mapping
653 $aMapeamento digital
700 1 $aMcBRATNEY, A. B.
700 1 $aHEMPEL, J.
700 1 $aMENDONÇA-SANTOS, M. de L.
700 1 $aMcKENZIE, N.
700 1 $aSANCHEZ, P.
700 1 $aGAN-LIN, Z.
700 1 $aMONTANARELLA, L.
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Registro original: |
Embrapa Solos (CNPS) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Gado de Leite. Para informações adicionais entre em contato com cnpgl.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Gado de Leite. |
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Data corrente: |
18/12/2019 |
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Data da última atualização: |
06/02/2024 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
ARAÚJO, R. S.; GARCIA, G. M.; VILELA, J. M. C.; ANDRADE, M. S.; OLIVEIRA, L. A. M.; KANO, E. K.; LANGE, C. C.; BRITO, M. A. V. P. E; BRANDAO, H. de M.; MOSQUEIRA, V. C. F. |
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Afiliação: |
RAQUEL SILVA ARAÚJO; GIANI MARTINS GARCIA; JOSÉ MARIO CARNEIRO VILELA; MARGARETH SPANGLER ANDRADE; LASER ANTÔNIO MACHADO OLIVEIRA; EUNICE KAZUE KANO; CARLA CHRISTINE LANGE, CNPGL; MARIA APARECIDA VASCONCELOS PAIVA E BRITO; HUMBERTO DE MELLO BRANDAO, CNPGL; VANESSA CARLA FURTADO MOSQUEIRA. |
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Título: |
Cloxacillin benzathine-loaded polymeric nanocapsules: Physicochemical characterization, cell uptake, and intramammary antimicrobial effect. |
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Ano de publicação: |
2019 |
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Fonte/Imprenta: |
Materials Science & Engineering C, v. 104, 110006, 2019. |
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DOI: |
https://doi.org/10.1016/j.msec.2019.110006 |
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Idioma: |
Inglês |
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Conteúdo: |
The present work shows the development and evaluation of the veterinary antibiotic cloxacillin benzathine(CLOXB) loaded into poly-ε-caprolactone (PCL) nanocapsules (NC), as a potential new treatment strategy tomanage bovine intramammary infections, such as mastitis.Staphylococcus aureus-induced mastitis is often arecurrent disease due to the persistence of bacteria within infected cells. CLOXB-PCL NC were prepared byinterfacial deposition of preformed biodegradable polymer followed by solvent displacement method. The meandiameter of NC varied from 241 to 428 nm and from 326 to 375 nm, when determined by dynamic light scat-tering and by atomic force microscopy, respectively. The zeta potential of NC was negative and varied from−28to−51 mV.In vitrorelease studies from the NC were performed in two media undersinkconditions: PBS with1% polyethylene glycol or milk. A reversed-phase HPLC method was developed to determine the NC entrapmentefficiency and kinetics of CLOXB release from the NC. Free CLOXB dissolution occurred very fast in both media,while drug release from the NC was slower and incomplete (below 50%) after 9 h. CLOXB release kinetics frompolymeric NC wasfitted with the Korsmeyer-Peppas model indicating that CLOXB release is governed by dif-fusion following Fick's law. Thefluorescence confocal microscopy images of macrophage-like J774A.1 cellsreveal NC uptake and internalizationin vitro. In addition, antimicrobial effect of the intramammary adminis-tration of CLOXB-PCL NC in cows with mastitis resulted in no clinical signs of toxicity and allowed completepathogen elimination after treatment. Thein vivoresults obtained in this work suggest that CLOXB-PCL NC couldbe a promising formulation for the treatment of intramammary infections in cattle, considering their physico-chemical properties, release profiles and effects on bovine mastitis control. MenosThe present work shows the development and evaluation of the veterinary antibiotic cloxacillin benzathine(CLOXB) loaded into poly-ε-caprolactone (PCL) nanocapsules (NC), as a potential new treatment strategy tomanage bovine intramammary infections, such as mastitis.Staphylococcus aureus-induced mastitis is often arecurrent disease due to the persistence of bacteria within infected cells. CLOXB-PCL NC were prepared byinterfacial deposition of preformed biodegradable polymer followed by solvent displacement method. The meandiameter of NC varied from 241 to 428 nm and from 326 to 375 nm, when determined by dynamic light scat-tering and by atomic force microscopy, respectively. The zeta potential of NC was negative and varied from−28to−51 mV.In vitrorelease studies from the NC were performed in two media undersinkconditions: PBS with1% polyethylene glycol or milk. A reversed-phase HPLC method was developed to determine the NC entrapmentefficiency and kinetics of CLOXB release from the NC. Free CLOXB dissolution occurred very fast in both media,while drug release from the NC was slower and incomplete (below 50%) after 9 h. CLOXB release kinetics frompolymeric NC wasfitted with the Korsmeyer-Peppas model indicating that CLOXB release is governed by dif-fusion following Fick's law. Thefluorescence confocal microscopy images of macrophage-like J774A.1 cellsreveal NC uptake and internalizationin vitro. In addition, antimicrobial effect of the intramammary adminis-tra... Mostrar Tudo |
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Palavras-Chave: |
Cell uptake; Cloxacillin benzathine; Intramammary; Release kinetics. |
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Thesaurus NAL: |
Mastitis; Nanocapsules. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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Marc: |
LEADER 02882naa a2200313 a 4500
001 2117206
005 2024-02-06
008 2019 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1016/j.msec.2019.110006$2DOI
100 1 $aARAÚJO, R. S.
245 $aCloxacillin benzathine-loaded polymeric nanocapsules$bPhysicochemical characterization, cell uptake, and intramammary antimicrobial effect.$h[electronic resource]
260 $c2019
520 $aThe present work shows the development and evaluation of the veterinary antibiotic cloxacillin benzathine(CLOXB) loaded into poly-ε-caprolactone (PCL) nanocapsules (NC), as a potential new treatment strategy tomanage bovine intramammary infections, such as mastitis.Staphylococcus aureus-induced mastitis is often arecurrent disease due to the persistence of bacteria within infected cells. CLOXB-PCL NC were prepared byinterfacial deposition of preformed biodegradable polymer followed by solvent displacement method. The meandiameter of NC varied from 241 to 428 nm and from 326 to 375 nm, when determined by dynamic light scat-tering and by atomic force microscopy, respectively. The zeta potential of NC was negative and varied from−28to−51 mV.In vitrorelease studies from the NC were performed in two media undersinkconditions: PBS with1% polyethylene glycol or milk. A reversed-phase HPLC method was developed to determine the NC entrapmentefficiency and kinetics of CLOXB release from the NC. Free CLOXB dissolution occurred very fast in both media,while drug release from the NC was slower and incomplete (below 50%) after 9 h. CLOXB release kinetics frompolymeric NC wasfitted with the Korsmeyer-Peppas model indicating that CLOXB release is governed by dif-fusion following Fick's law. Thefluorescence confocal microscopy images of macrophage-like J774A.1 cellsreveal NC uptake and internalizationin vitro. In addition, antimicrobial effect of the intramammary adminis-tration of CLOXB-PCL NC in cows with mastitis resulted in no clinical signs of toxicity and allowed completepathogen elimination after treatment. Thein vivoresults obtained in this work suggest that CLOXB-PCL NC couldbe a promising formulation for the treatment of intramammary infections in cattle, considering their physico-chemical properties, release profiles and effects on bovine mastitis control.
650 $aMastitis
650 $aNanocapsules
653 $aCell uptake
653 $aCloxacillin benzathine
653 $aIntramammary
653 $aRelease kinetics
700 1 $aGARCIA, G. M.
700 1 $aVILELA, J. M. C.
700 1 $aANDRADE, M. S.
700 1 $aOLIVEIRA, L. A. M.
700 1 $aKANO, E. K.
700 1 $aLANGE, C. C.
700 1 $aBRITO, M. A. V. P. E
700 1 $aBRANDAO, H. de M.
700 1 $aMOSQUEIRA, V. C. F.
773 $tMaterials Science & Engineering C$gv. 104, 110006, 2019.
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