LC UV methodology for simultaneous.

Registro completo de metadados
MetadadosDescriçãoIdioma
Autor(es): dc.creatorSouza, Jacqueline de-
Autor(es): dc.creatorKano, Eunice Kazue-
Autor(es): dc.creatorKoono, Eunice Emiko Mori-
Autor(es): dc.creatorSchramm, Simone Grigoleto-
Autor(es): dc.creatorPorta, Valentina-
Autor(es): dc.creatorStorpirtis, Sílvia-
Data de aceite: dc.date.accessioned2025-08-21T15:07:48Z-
Data de disponibilização: dc.date.available2025-08-21T15:07:48Z-
Data de envio: dc.date.issued2017-03-20-
Data de envio: dc.date.issued2017-03-20-
Data de envio: dc.date.issued2008-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/handle/123456789/7399-
Fonte completa do material: dc.identifierhttp://link.springer.com/article/10.1365/s10337-008-0913-y-
Fonte completa do material: dc.identifierhttps://doi.org/10.1365/s10337-008-0913-y-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1003083-
Descrição: dc.descriptionThis study describes an accurate, sensitive, and specific chromatographic method for the simultaneous quantitative determination of lamivudine and zidovudine in human blood plasma, using stavudine as an internal standard. The chromatographic separation was performed using a C8 column (150 9 4.6 mm, 5 lm), and ultraviolet absorbency detection at 270 nm with gradient elution. Two mobile phases were used. Phase A contained 10 mM potassium phosphate and 3% acetonitrile, whereas Phase B contained methanol. A linear gradient was used with a variability of A-B phase proportion from 98–2% to 72–28%, respectively. The drug extraction was performed with two 4 mL aliquots of ethyl acetate.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Direitos: dc.rightsrestrito-
Palavras-chave: dc.subjectColumn liquid chromatography-
Palavras-chave: dc.subjectLamivudine-
Palavras-chave: dc.subjectZidovudine-
Palavras-chave: dc.subjectStavudine-
Título: dc.titleLC UV methodology for simultaneous.-
Aparece nas coleções:Repositório Institucional - UFOP

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