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Artigo de periodico
Effect of different sampling schedules on results of bioavailability and bioequivalence studies: evaluation by means of Monte Carlo simulations (2017)
Kano, Eunice Kazue; Chiann, Chang ; Fukuda, Kazuo; Porta, Valentina
Source: Drug Research. Unidades: FCF, IME
Subjects: FARMACOCINÉTICA, BIODISPONIBILIDADE, BIOEQUIVALÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KANO, Eunice Kazue et al. Effect of different sampling schedules on results of bioavailability and bioequivalence studies: evaluation by means of Monte Carlo simulations. Drug Research, v. 67, n. 8, p. 451-457, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0043-105797. Acesso em: 12 nov. 2024.
APA
Kano, E. K., Chiann, C., Fukuda, K., & Porta, V. (2017). Effect of different sampling schedules on results of bioavailability and bioequivalence studies: evaluation by means of Monte Carlo simulations. Drug Research, 67( 8), 451-457. doi:10.1055/s-0043-105797
NLM
Kano EK, Chiann C, Fukuda K, Porta V. Effect of different sampling schedules on results of bioavailability and bioequivalence studies: evaluation by means of Monte Carlo simulations [Internet]. Drug Research. 2017 ; 67( 8): 451-457.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1055/s-0043-105797
Vancouver
Kano EK, Chiann C, Fukuda K, Porta V. Effect of different sampling schedules on results of bioavailability and bioequivalence studies: evaluation by means of Monte Carlo simulations [Internet]. Drug Research. 2017 ; 67( 8): 451-457.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1055/s-0043-105797
Artigo de periodico
Average bioequivalence of single 500 mg doses of two oral formulations of levofloxacin: a randomized, open-label, two-period crossover study in healthy adult Brazilian volunteers (2015)
Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Schramm, Simone Grigoleto; Serra, Cristina Helena dos Reis ; Abib Junior, Eduardo; Pereira, Renata; Freitas, Marcia Sayuri Takamatsu; Iecco, Maria Cristina; Porta, Valentina
Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: FCF
Subjects: BIOEQUIVALÊNCIA, FARMACOCINÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KANO, Eunice Kazue et al. Average bioequivalence of single 500 mg doses of two oral formulations of levofloxacin: a randomized, open-label, two-period crossover study in healthy adult Brazilian volunteers. Brazilian Journal of Pharmaceutical Sciences, v. 51, n. 1, p. 503-511, 2015Tradução . . Disponível em: https://doi.org/10.1590/S1984-82502015000100020. Acesso em: 12 nov. 2024.
APA
Kano, E. K., Koono, E. E. M., Schramm, S. G., Serra, C. H. dos R., Abib Junior, E., Pereira, R., et al. (2015). Average bioequivalence of single 500 mg doses of two oral formulations of levofloxacin: a randomized, open-label, two-period crossover study in healthy adult Brazilian volunteers. Brazilian Journal of Pharmaceutical Sciences, 51( 1), 503-511. doi:10.1590/S1984-82502015000100020
NLM
Kano EK, Koono EEM, Schramm SG, Serra CH dos R, Abib Junior E, Pereira R, Freitas MST, Iecco MC, Porta V. Average bioequivalence of single 500 mg doses of two oral formulations of levofloxacin: a randomized, open-label, two-period crossover study in healthy adult Brazilian volunteers [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51( 1): 503-511.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1590/S1984-82502015000100020
Vancouver
Kano EK, Koono EEM, Schramm SG, Serra CH dos R, Abib Junior E, Pereira R, Freitas MST, Iecco MC, Porta V. Average bioequivalence of single 500 mg doses of two oral formulations of levofloxacin: a randomized, open-label, two-period crossover study in healthy adult Brazilian volunteers [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51( 1): 503-511.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1590/S1984-82502015000100020
Artigo de periodico
Metronidazole immediate release formulations: A fasting randomized open-label crossover bioequivalence study in healthy volunteers (2012)
Freitas Silva, M; Schramm, Simone Grigoleto; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Manfio, Josélia Larger; Porta, Valentina ; Serra, Cristina Helena dos Reis
Source: Arzneimittelforschung Drug Research. Unidade: FCF
Subjects: BIODISPONIBILIDADE, FARMACOCINÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS SILVA, M et al. Metronidazole immediate release formulations: A fasting randomized open-label crossover bioequivalence study in healthy volunteers. Arzneimittelforschung Drug Research, v. 62, n. 10, p. 490-495, 2012Tradução . . Acesso em: 12 nov. 2024.
APA
Freitas Silva, M., Schramm, S. G., Kano, E. K., Koono, E. E. M., Manfio, J. L., Porta, V., & Serra, C. H. dos R. (2012). Metronidazole immediate release formulations: A fasting randomized open-label crossover bioequivalence study in healthy volunteers. Arzneimittelforschung Drug Research, 62( 10), 490-495.
NLM
Freitas Silva M, Schramm SG, Kano EK, Koono EEM, Manfio JL, Porta V, Serra CH dos R. Metronidazole immediate release formulations: A fasting randomized open-label crossover bioequivalence study in healthy volunteers. Arzneimittelforschung Drug Research. 2012 ; 62( 10): 490-495.[citado 2024 nov. 12 ]
Vancouver
Freitas Silva M, Schramm SG, Kano EK, Koono EEM, Manfio JL, Porta V, Serra CH dos R. Metronidazole immediate release formulations: A fasting randomized open-label crossover bioequivalence study in healthy volunteers. Arzneimittelforschung Drug Research. 2012 ; 62( 10): 490-495.[citado 2024 nov. 12 ]
Artigo de periodico
An efficient HPLC-UV method for the quantitative determination of cefadroxil in human plasma and its application in pharmacokinetic studies (2012)
Kano, Eunice Kazue; Serra, Cristina Helena dos Reis ; Koono, Eunice Emiko Mori; Fukuda, Kazuo; Porta, Valentina
Source: Journal of Liquid Chromatography & Related Technologies. Unidade: FCF
Subjects: BIODISPONIBILIDADE, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, FARMACOCINÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KANO, Eunice Kazue et al. An efficient HPLC-UV method for the quantitative determination of cefadroxil in human plasma and its application in pharmacokinetic studies. Journal of Liquid Chromatography & Related Technologies, v. 35, n. 13, p. 1871-1881, 2012Tradução . . Disponível em: https://doi.org/10.1080/10826076.2011.627607. Acesso em: 12 nov. 2024.
APA
Kano, E. K., Serra, C. H. dos R., Koono, E. E. M., Fukuda, K., & Porta, V. (2012). An efficient HPLC-UV method for the quantitative determination of cefadroxil in human plasma and its application in pharmacokinetic studies. Journal of Liquid Chromatography & Related Technologies, 35( 13), 1871-1881. doi:10.1080/10826076.2011.627607
NLM
Kano EK, Serra CH dos R, Koono EEM, Fukuda K, Porta V. An efficient HPLC-UV method for the quantitative determination of cefadroxil in human plasma and its application in pharmacokinetic studies [Internet]. Journal of Liquid Chromatography & Related Technologies. 2012 ; 35( 13): 1871-1881.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1080/10826076.2011.627607
Vancouver
Kano EK, Serra CH dos R, Koono EEM, Fukuda K, Porta V. An efficient HPLC-UV method for the quantitative determination of cefadroxil in human plasma and its application in pharmacokinetic studies [Internet]. Journal of Liquid Chromatography & Related Technologies. 2012 ; 35( 13): 1871-1881.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1080/10826076.2011.627607
Artigo de periodico
HPLC-FLD methods to quantify chloroaluminum phthalocyanine in nanoparticles, plasma and tissue: application in pharmacokinetic and biodistribution studies (2011)
Oliveira,Líliam Teixeira; Garcia, Giani Martins; Kano, Eunice Kazue; Tedesco, Antonio Claudio; Mosqueira, Vanessa Carla Furtado
Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FCF, FFCLRP
Subjects: TERAPIA FOTODINÂMICA, NANOPARTÍCULAS, FLUORESCÊNCIA, CROMATOGRAFIA LÍQUIDA, FARMACOCINÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Líliam Teixeira et al. HPLC-FLD methods to quantify chloroaluminum phthalocyanine in nanoparticles, plasma and tissue: application in pharmacokinetic and biodistribution studies. Journal of Pharmaceutical and Biomedical Analysis, v. 56, n. 1, p. 70-77, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2011.04.016. Acesso em: 12 nov. 2024.
APA
Oliveira, L. T., Garcia, G. M., Kano, E. K., Tedesco, A. C., & Mosqueira, V. C. F. (2011). HPLC-FLD methods to quantify chloroaluminum phthalocyanine in nanoparticles, plasma and tissue: application in pharmacokinetic and biodistribution studies. Journal of Pharmaceutical and Biomedical Analysis, 56( 1), 70-77. doi:10.1016/j.jpba.2011.04.016
NLM
Oliveira LT, Garcia GM, Kano EK, Tedesco AC, Mosqueira VCF. HPLC-FLD methods to quantify chloroaluminum phthalocyanine in nanoparticles, plasma and tissue: application in pharmacokinetic and biodistribution studies [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2011 ; 56( 1): 70-77.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.jpba.2011.04.016
Vancouver
Oliveira LT, Garcia GM, Kano EK, Tedesco AC, Mosqueira VCF. HPLC-FLD methods to quantify chloroaluminum phthalocyanine in nanoparticles, plasma and tissue: application in pharmacokinetic and biodistribution studies [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2011 ; 56( 1): 70-77.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.jpba.2011.04.016
Artigo de periodico
Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers (2010)
Silva, Marina de Freitas; Schramm, Simone Grigoleto; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Porta, Valentina ; Serra, Cristina Helena dos Reis
Source: Clinical Therapeutics. Unidade: FCF
Subjects: BIOEQUIVALÊNCIA, FARMACOCINÉTICA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Marina de Freitas et al. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers. Clinical Therapeutics, v. 32, n. 4, p. 758-765, 2010Tradução . . Disponível em: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf. Acesso em: 12 nov. 2024.
APA
Silva, M. de F., Schramm, S. G., Kano, E. K., Koono, E. E. M., Porta, V., & Serra, C. H. dos R. (2010). Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers. Clinical Therapeutics, 32( 4), 758-765. Recuperado de http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
NLM
Silva M de F, Schramm SG, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers [Internet]. Clinical Therapeutics. 2010 ; 32( 4): 758-765.[citado 2024 nov. 12 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
Vancouver
Silva M de F, Schramm SG, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers [Internet]. Clinical Therapeutics. 2010 ; 32( 4): 758-765.[citado 2024 nov. 12 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
Tese (Doutorado)
Avaliação de diferentes cronogramas de coletas de amostras biológicas em estudos de bioequivalência e análise da influência do teor de fármaco sobre os resultados destes estudos (2008)
Kano, Eunice Kazue; Porta, Valentina (Orientador)
Unidade: FCF
Subjects: BIOEQUIVALÊNCIA, FARMACOCINÉTICA, FÁRMACOS (ESTUDO CLÍNICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KANO, Eunice Kazue. Avaliação de diferentes cronogramas de coletas de amostras biológicas em estudos de bioequivalência e análise da influência do teor de fármaco sobre os resultados destes estudos. 2008. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2008. Disponível em: http://www.teses.usp.br/teses/disponiveis/9/9139/tde-27052008-104740/. Acesso em: 12 nov. 2024.
APA
Kano, E. K. (2008). Avaliação de diferentes cronogramas de coletas de amostras biológicas em estudos de bioequivalência e análise da influência do teor de fármaco sobre os resultados destes estudos (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/9/9139/tde-27052008-104740/
NLM
Kano EK. Avaliação de diferentes cronogramas de coletas de amostras biológicas em estudos de bioequivalência e análise da influência do teor de fármaco sobre os resultados destes estudos [Internet]. 2008 ;[citado 2024 nov. 12 ] Available from: http://www.teses.usp.br/teses/disponiveis/9/9139/tde-27052008-104740/
Vancouver
Kano EK. Avaliação de diferentes cronogramas de coletas de amostras biológicas em estudos de bioequivalência e análise da influência do teor de fármaco sobre os resultados destes estudos [Internet]. 2008 ;[citado 2024 nov. 12 ] Available from: http://www.teses.usp.br/teses/disponiveis/9/9139/tde-27052008-104740/

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