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Registro Completo |
Biblioteca(s): |
Embrapa Pecuária Sudeste; Embrapa Solos. |
Data corrente: |
23/02/2017 |
Data da última atualização: |
10/11/2021 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
GONZALEZ, M. H.; SILVA, C. S. da; AMARAL, C. D. B.; BIANCHI, S. R.; OLIVEIRA, L. H. B. de; COELHO, J. S.; OLIVEIRA, A.; NOGUEIRA, A. R. de A. |
Afiliação: |
Mario Henrique Gonzalez, UNESP; Caroline Santos da Silva, UFSCar; Clarice Dias Britto do Amaral, UFSCar; SILMARA ROSSANA BIANCHI, CNPS; Luciano Henrique Barca de Oliveira, UNESP; Jessica Silva Coelho, UNESP; Andrea Oliveira, UFPR; ANA RITA DE ARAUJO NOGUEIRA, CPPSE. |
Título: |
Determination of elemental impurities in acyclovir ointment and raw materials using microwave acid digestion (MW-AD) and ICP-MS. |
Ano de publicação: |
2017 |
Fonte/Imprenta: |
Journal of the Brazilian Chemical Society, v. 28, n. 1, p. 98-105, 2017. |
DOI: |
https://doi.org/10.5935/0103-5053.20160151 |
Idioma: |
Inglês Português |
Conteúdo: |
Inorganic elements present in pharmaceutical products were determined by inductively coupled plasma-mass spectrometer (ICP-MS), employing microwave acid digestion as a sample preparation method. The most abundant isotopes, 75As+ , 65Cu+ , 52Cr+ , 58Ni+ , 208Pb+ , and 51V+ , were determined in acyclovir ointment and its constituents. Elemental impurities in the pharmaceutical samples were determined using an inductively coupled plasma-universal cell technology-mass spectrometer (ICP-UCT-MS) operated in kinetic energy discrimination (KED) and standard mode. The accuracy of the method was assessed by means of addition and recovery experiments. Except for Cr, spiked recoveries of the elements added to the samples before microwave acid digestion (MW-AD) step were between 95.1 and 126%, and after MW-AD step ranged from 85.6 to 132%. Limits of detection (LOD) obtained by proposed method is in agreement to those required by the U.S. Pharmacopeia Convention (USP), showing that the ICP-MS technique is well suited for quantification of these elements. The LOD's (ng L-1) for 51V+ , 52Cr+ , 58Ni+ , 65Cu+ , 75As+ and 208Pb+ in 1% v v-1 HNO3 medium were: 2.2, 81.3, 91.9, 6.9, 0.2 and 3.1, respectively. The concentration of the analytes in these samples presented a wide range, varying from 2.3 ± 0.8 µg kg-1 for As to 3446 ± 47 µg kg-1 for Cr. |
Palavras-Chave: |
Acyclovir; Elemental impurity; Impureza elementar; Pharmaceutical product; Produto farmacêutico. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/156641/1/0103-5053-jbchs-28-01-0098.pdf
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Marc: |
LEADER 02269naa a2200277 a 4500 001 2067515 005 2021-11-10 008 2017 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.5935/0103-5053.20160151$2DOI 100 1 $aGONZALEZ, M. H. 245 $aDetermination of elemental impurities in acyclovir ointment and raw materials using microwave acid digestion (MW-AD) and ICP-MS.$h[electronic resource] 260 $c2017 520 $aInorganic elements present in pharmaceutical products were determined by inductively coupled plasma-mass spectrometer (ICP-MS), employing microwave acid digestion as a sample preparation method. The most abundant isotopes, 75As+ , 65Cu+ , 52Cr+ , 58Ni+ , 208Pb+ , and 51V+ , were determined in acyclovir ointment and its constituents. Elemental impurities in the pharmaceutical samples were determined using an inductively coupled plasma-universal cell technology-mass spectrometer (ICP-UCT-MS) operated in kinetic energy discrimination (KED) and standard mode. The accuracy of the method was assessed by means of addition and recovery experiments. Except for Cr, spiked recoveries of the elements added to the samples before microwave acid digestion (MW-AD) step were between 95.1 and 126%, and after MW-AD step ranged from 85.6 to 132%. Limits of detection (LOD) obtained by proposed method is in agreement to those required by the U.S. Pharmacopeia Convention (USP), showing that the ICP-MS technique is well suited for quantification of these elements. The LOD's (ng L-1) for 51V+ , 52Cr+ , 58Ni+ , 65Cu+ , 75As+ and 208Pb+ in 1% v v-1 HNO3 medium were: 2.2, 81.3, 91.9, 6.9, 0.2 and 3.1, respectively. The concentration of the analytes in these samples presented a wide range, varying from 2.3 ± 0.8 µg kg-1 for As to 3446 ± 47 µg kg-1 for Cr. 653 $aAcyclovir 653 $aElemental impurity 653 $aImpureza elementar 653 $aPharmaceutical product 653 $aProduto farmacêutico 700 1 $aSILVA, C. S. da 700 1 $aAMARAL, C. D. B. 700 1 $aBIANCHI, S. R. 700 1 $aOLIVEIRA, L. H. B. de 700 1 $aCOELHO, J. S. 700 1 $aOLIVEIRA, A. 700 1 $aNOGUEIRA, A. R. de A. 773 $tJournal of the Brazilian Chemical Society$gv. 28, n. 1, p. 98-105, 2017.
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Registro original: |
Embrapa Solos (CNPS) |
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Registro Completo
Biblioteca(s): |
Embrapa Arroz e Feijão. |
Data corrente: |
21/12/2020 |
Data da última atualização: |
20/12/2022 |
Tipo da produção científica: |
Nota Técnica/Nota Científica |
Autoria: |
BRAY, A. W.; KIM, J. H.; SCHRUMPF, M.; PEACOCK, C.; BANWART, S.; SCHIPPER, L.; ANGERS, D.; CHIRINDA, N.; ZINN, Y. L.; ALBRECHT, A.; KUIKMAN, P.; JOUQUET, P.; DEMENOIS, J.; FARRELL, M.; SOUSSANA, J.-F.; KUHNERT, M.; MILNE, E.; FONTAINE, S.; TAGHIZADEH-TOOSI, A.; CERRI, C. E. P.; CORBEELS, M.; CARDINAEL, R.; CERVANTES, V. A.; OLESEN, J. E.; BATJES, N.; HEUVELINK, G.; MAIA, S. M. F.; KEESSTRA, S.; CLAESSEN, L.; MADARI, B. E.; VERCHOT, L.; NIE, W.; BRUNELLE, T.; MORAN, D.; FRANK, S.; BODLE, R.; FRELIH-LARSEN, A.; DOUGILL, A.; MONTANARELLA, L.; STRINGER, L.; CHENU, C.; HIEDERER, R.; SMITH, P.; ARIAS-NAVARRO, C. |
Afiliação: |
ANDREW W. BRAY; JOHN H. KIM; MARION SCHRUMPF; CAROLINE PEACOCK; STEVEN BANWART; LOUIS SCHIPPER; DENIS ANGERS; NGONIDZASHE CHIRINDA; YURI LOPES ZINN; ALAIN ALBRECHT; PETER KUIKMAN; PASCAL JOUQUET; JULIEN DEMENOIS; MARK FARRELL; JEAN-FRANCOIS SOUSSANA; MATTHIAS KUHNERT; ELEANOR MILNE; SEBASTIEN FONTAINE; AREZOO TAGHIZADEH-TOOSI; CARLOS EDUARDO PELLEGRINO CERRI; MARC CORBEELS; REMI CARDINAEL; VIRIDIANA ALCÁNTARA CERVANTES; JØRGEN E. OLESEN; NIELS BATJES; GERARD HEUVELINK; STOÉCIO MALTA FERREIRA MAIA; SASKIA KEESSTRA; LIEVEN CLAESSEN; BEATA EMOKE MADARI, CNPAF; LOUIS VERCHOT; WAN NIE; THIERRY BRUNELLE; DOMINIC MORAN; STEFAN FRANK; RALPH BODLE; ANA FRELIH-LARSEN; ANDREW DOUGILL; LUCA MONTANARELLA; LINDSAY STRINGER; CLAIRE CHENU; ROLAND HIEDERER; PETE SMITH; CRISTINA ARIAS-NAVARRO. |
Título: |
The science base of a strategic research agenda: executive summary. |
Ano de publicação: |
2019 |
Fonte/Imprenta: |
Wageningen: CIRCASA, 2019. |
Páginas: |
15 p. |
DOI: |
https://doi.org/10.15454/YUFPFD |
Idioma: |
Inglês |
Notas: |
European Union's Horizon 2020 Research and Innovation Programme Grant Agreement No 774378. Coordination of International Research Cooperation on Soil Carbon Sequestration in Agriculture. |
Conteúdo: |
Identifying the challenges around soil organic carbon sequestration in agriculture. Questionnaire. Twelve Testable Hypotheses for Soil Organic Carbon Sequestration in Agriculture. Key research and innovation advances. |
Thesagro: |
Carbono; Solo. |
Thesaurus NAL: |
Carbon sequestration; Research and development; Soil organic carbon. |
Categoria do assunto: |
P Recursos Naturais, Ciências Ambientais e da Terra |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/219512/1/D1.3-The-science-base-of-a-strategic-research-agenda.pdf
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Marc: |
LEADER 02217nam a2200721 a 4500 001 2128518 005 2022-12-20 008 2019 bl uuuu u0uu1 u #d 024 7 $ahttps://doi.org/10.15454/YUFPFD$2DOI 100 1 $aBRAY, A. W. 245 $aThe science base of a strategic research agenda$bexecutive summary.$h[electronic resource] 260 $aWageningen: CIRCASA$c2019 300 $a15 p. 500 $aEuropean Union's Horizon 2020 Research and Innovation Programme Grant Agreement No 774378. Coordination of International Research Cooperation on Soil Carbon Sequestration in Agriculture. 520 $aIdentifying the challenges around soil organic carbon sequestration in agriculture. Questionnaire. Twelve Testable Hypotheses for Soil Organic Carbon Sequestration in Agriculture. Key research and innovation advances. 650 $aCarbon sequestration 650 $aResearch and development 650 $aSoil organic carbon 650 $aCarbono 650 $aSolo 700 1 $aKIM, J. H. 700 1 $aSCHRUMPF, M. 700 1 $aPEACOCK, C. 700 1 $aBANWART, S. 700 1 $aSCHIPPER, L. 700 1 $aANGERS, D. 700 1 $aCHIRINDA, N. 700 1 $aZINN, Y. L. 700 1 $aALBRECHT, A. 700 1 $aKUIKMAN, P. 700 1 $aJOUQUET, P. 700 1 $aDEMENOIS, J. 700 1 $aFARRELL, M. 700 1 $aSOUSSANA, J.-F. 700 1 $aKUHNERT, M. 700 1 $aMILNE, E. 700 1 $aFONTAINE, S. 700 1 $aTAGHIZADEH-TOOSI, A. 700 1 $aCERRI, C. E. P. 700 1 $aCORBEELS, M. 700 1 $aCARDINAEL, R. 700 1 $aCERVANTES, V. A. 700 1 $aOLESEN, J. E. 700 1 $aBATJES, N. 700 1 $aHEUVELINK, G. 700 1 $aMAIA, S. M. F. 700 1 $aKEESSTRA, S. 700 1 $aCLAESSEN, L. 700 1 $aMADARI, B. E. 700 1 $aVERCHOT, L. 700 1 $aNIE, W. 700 1 $aBRUNELLE, T. 700 1 $aMORAN, D. 700 1 $aFRANK, S. 700 1 $aBODLE, R. 700 1 $aFRELIH-LARSEN, A. 700 1 $aDOUGILL, A. 700 1 $aMONTANARELLA, L. 700 1 $aSTRINGER, L. 700 1 $aCHENU, C. 700 1 $aHIEDERER, R. 700 1 $aSMITH, P. 700 1 $aARIAS-NAVARRO, C.
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