Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Cromatografia líquida de alta eficiência/fase reversa/análise quantitativa"'
Autor:
Janaíne Micheli Chassot, Luana Mota Ferreira, Felipe Pereira Gomes, Letícia Cruz, Leandro Tasso
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 51, Iss 4, Pp 803-810 (2015)
abstract A simple stability-indicating RP-HPLC/UV method was validated for determination of beclomethasone dipropionate (BD) in nanocapsule suspensions. Chromatographic conditions consisted of a RP C18column (250 mm x 4.60 mm, 5 µm, 110 Å), using m
Externí odkaz:
https://doaj.org/article/f7d2fab6cb2642eaa9d03ce088adc154
Autor:
Lis Marie Monteiro, Guilherme Diniz Tavares, Elizabeth Igne Ferreira, Vladi Olga Consiglieri, Nadia Araci Bou-Chacra, Raimar Löbenberg
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 51, Iss 3, Pp 561-567 (2015)
Hydroxymethylnitrofurazone (NFOH) is a new compound with potential leishmanicidal and trypanocidal activity. Despite its effectiveness, the formulators have to overcome its poor aqueous solubility. Recently, polymeric nano-scale drug delivery systems
Externí odkaz:
https://doaj.org/article/b0b4203dce2f4996bd3890ab7bf8e3c6
Autor:
Vanita Somasekhar
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 50, Iss 4, Pp 793-797 (2014)
A reverse phase HPLC method is described for the determination of 6-mercaptopurine in bulk and tablets. Chromatography was carried on a C18 column using a mixture of acetonitrile and 0.05 mol/L sodium acetate buffer (10:90 v/v) as the mobile phase at
Externí odkaz:
https://doaj.org/article/47dfd25f8f224fa3975cb8f3f35ae07b
Autor:
Ramakrishna Kommana, Gouthami Kannabattula, Sunitha Gurrala, Venkat Raj Yeradesi, Panikumar Anumolu Durga
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 50, Iss 4, Pp 895-901 (2014)
A simple, specific, precise, accurate, linear, rapid, economic and validated stability indicating an RP-HPLC method for the simultaneous quantification of cefepime and tazobactam in a dry injection dosage form has been developed. Separation was perfo
Externí odkaz:
https://doaj.org/article/2a8f3b7cc5c44bbfbcab4f4bc8099828
Autor:
Sunitha Gurrala, Panikumar Anumolu Durga, Ramakrishna Kommana, Venkat Raj Yeradesi, Gouthami Kannabattula
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Volume: 50, Issue: 4, Pages: 895-901, Published: DEC 2014
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 No. 4 (2014); 895-901
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 Núm. 4 (2014); 895-901
Brazilian Journal of Pharmaceutical Sciences; v. 50 n. 4 (2014); 895-901
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Vol 50, Iss 4, Pp 895-901 (2014)
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 No. 4 (2014); 895-901
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 Núm. 4 (2014); 895-901
Brazilian Journal of Pharmaceutical Sciences; v. 50 n. 4 (2014); 895-901
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Vol 50, Iss 4, Pp 895-901 (2014)
Desenvolveu-se método específico, preciso, exato, linear, rápido e econômico, de validação de estabilidade, indicando o método de CLAE-FR para a quantificação simultânea de cefepima e tazobactam na forma de dosagem injetável seca. A separa
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 No. 1 (2014); 213-223
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 Núm. 1 (2014); 213-223
Brazilian Journal of Pharmaceutical Sciences; v. 50 n. 1 (2014); 213-223
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Volume: 50, Issue: 1, Pages: 213-223, Published: MAR 2014
Web of Science
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 No. 1 (2014); 213-223
Brazilian Journal of Pharmaceutical Sciences; Vol. 50 Núm. 1 (2014); 213-223
Brazilian Journal of Pharmaceutical Sciences; v. 50 n. 1 (2014); 213-223
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Volume: 50, Issue: 1, Pages: 213-223, Published: MAR 2014
Web of Science
A reversed-phase high performance liquid chromatography method was validated for the determination of cefazolin sodium in lyophilized powder for solution for injection to be applied for quality control in pharmaceutical industry. The liquid chromatog
Autor:
Elizabeth Igne Ferreira, Vladi Olga Consiglieri, Nadia Araci Bou-Chacra, Guilherme Diniz Tavares, Lis Marie Monteiro, Raimar Löbenberg
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Volume: 51, Issue: 3, Pages: 561-567, Published: SEP 2015
Brazilian Journal of Pharmaceutical Sciences, Vol 51, Iss 3, Pp 561-567 (2015)
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 No. 3 (2015); 561-567
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 Núm. 3 (2015); 561-567
Brazilian Journal of Pharmaceutical Sciences; v. 51 n. 3 (2015); 561-567
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Vol 51, Iss 3, Pp 561-567 (2015)
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 No. 3 (2015); 561-567
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 Núm. 3 (2015); 561-567
Brazilian Journal of Pharmaceutical Sciences; v. 51 n. 3 (2015); 561-567
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Hidroximetilnitrofural (NFOH) é um novo composto que possui atividade leishmanicida e tripanomicida potencial. Um método apropriado foi desenvolvido e validado para a determinação de NFOH em nanopartículas de poli(n-butil cianoacrilato) (PBCA).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec17ef1be5f2739aab6128936e695e31
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502015000300561&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502015000300561&lng=en&tlng=en
Validation of analytical methodology for quantification of cefazolin sodium by liquid chromatography
Publikováno v:
Currículo Lattes
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
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Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::b59f4c6d0a387a7f5956282dc5b46131