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Filtros : "FCF" "ARTIGO DE PERIODICO" "Porta, Valentina" Removido: "Irã" Limpar

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  • Artigo de periodico

    In silico prediction of plasma concentrations of Fluconazole capsules with different dissolution profiles and bioequivalence study using population simulation (2019)

    Duque, Marcelo Dutra; Silva, Daniela Amaral; Issa, Michele Georges ; Porta, Valentina ; Löbenberg, Raimar ; Ferraz, Humberto Gomes

    Source: Pharmaceutics. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, FARMACOCINÉTICA

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    • ABNT

      DUQUE, Marcelo Dutra et al. In silico prediction of plasma concentrations of Fluconazole capsules with different dissolution profiles and bioequivalence study using population simulation. Pharmaceutics, v. 11, p. 1-12 art. 215, 2019Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics11050215. Acesso em: 21 maio 2024.

    • APA

      Duque, M. D., Silva, D. A., Issa, M. G., Porta, V., Löbenberg, R., & Ferraz, H. G. (2019). In silico prediction of plasma concentrations of Fluconazole capsules with different dissolution profiles and bioequivalence study using population simulation. Pharmaceutics, 11, 1-12 art. 215. doi:10.3390/pharmaceutics11050215

    • NLM

      Duque MD, Silva DA, Issa MG, Porta V, Löbenberg R, Ferraz HG. In silico prediction of plasma concentrations of Fluconazole capsules with different dissolution profiles and bioequivalence study using population simulation [Internet]. Pharmaceutics. 2019 ; 11 1-12 art. 215.[citado 2024 maio 21 ] Available from: https://doi.org/10.3390/pharmaceutics11050215

    • Vancouver

      Duque MD, Silva DA, Issa MG, Porta V, Löbenberg R, Ferraz HG. In silico prediction of plasma concentrations of Fluconazole capsules with different dissolution profiles and bioequivalence study using population simulation [Internet]. Pharmaceutics. 2019 ; 11 1-12 art. 215.[citado 2024 maio 21 ] Available from: https://doi.org/10.3390/pharmaceutics11050215

  • 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

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    • 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: 21 maio 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 maio 21 ] 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 maio 21 ] 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

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    • 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: 21 maio 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 maio 21 ] 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 maio 21 ] Available from: https://doi.org/10.1590/S1984-82502015000100020

  • Artigo de periodico

    Dissolution efficiency and bioequivalence study using urine data from healthy volunteers: a comparison between two tablet formulations of cephalexin (2015)

    Serra, Cristina Helena dos Reis ; Chang, Kyung Hee; Dezani, Thaisa Marinho; Porta, Valentina ; Storpirtis, Silvia

    Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, COMPRIMIDOS

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    • ABNT

      SERRA, Cristina Helena dos Reis et al. Dissolution efficiency and bioequivalence study using urine data from healthy volunteers: a comparison between two tablet formulations of cephalexin. Brazilian Journal of Pharmaceutical Sciences, v. 51, n. 2, p. 383-392, 2015Tradução . . Disponível em: https://doi.org/10.1590/s1984-82502015000200016. Acesso em: 21 maio 2024.

    • APA

      Serra, C. H. dos R., Chang, K. H., Dezani, T. M., Porta, V., & Storpirtis, S. (2015). Dissolution efficiency and bioequivalence study using urine data from healthy volunteers: a comparison between two tablet formulations of cephalexin. Brazilian Journal of Pharmaceutical Sciences, 51( 2), 383-392. doi:10.1590/s1984-82502015000200016

    • NLM

      Serra CH dos R, Chang KH, Dezani TM, Porta V, Storpirtis S. Dissolution efficiency and bioequivalence study using urine data from healthy volunteers: a comparison between two tablet formulations of cephalexin [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51( 2): 383-392.[citado 2024 maio 21 ] Available from: https://doi.org/10.1590/s1984-82502015000200016

    • Vancouver

      Serra CH dos R, Chang KH, Dezani TM, Porta V, Storpirtis S. Dissolution efficiency and bioequivalence study using urine data from healthy volunteers: a comparison between two tablet formulations of cephalexin [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51( 2): 383-392.[citado 2024 maio 21 ] Available from: https://doi.org/10.1590/s1984-82502015000200016

  • Artigo de periodico

    Pharmacokinetics and bioequivalence evaluation of cyclobenzaprine tablets (2013)

    Brioschi, Tatiane Maria de Lima Souza; Schramm, Simone Grigoleto; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Ching, Ting Hui; Serra, Cristina Helena dos Reis ; Porta, Valentina

    Source: BioMed Research International. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, FARMACOGENÉTICA

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      BRIOSCHI, Tatiane Maria de Lima Souza et al. Pharmacokinetics and bioequivalence evaluation of cyclobenzaprine tablets. BioMed Research International, v. 2013, p. 1-6, 2013Tradução . . Disponível em: https://doi.org/10.1155/2013/281392. Acesso em: 21 maio 2024.

    • APA

      Brioschi, T. M. de L. S., Schramm, S. G., Kano, E. K., Koono, E. E. M., Ching, T. H., Serra, C. H. dos R., & Porta, V. (2013). Pharmacokinetics and bioequivalence evaluation of cyclobenzaprine tablets. BioMed Research International, 2013, 1-6. doi:10.1155/2013/281392

    • NLM

      Brioschi TM de LS, Schramm SG, Kano EK, Koono EEM, Ching TH, Serra CH dos R, Porta V. Pharmacokinetics and bioequivalence evaluation of cyclobenzaprine tablets [Internet]. BioMed Research International. 2013 ; 2013 1-6.[citado 2024 maio 21 ] Available from: https://doi.org/10.1155/2013/281392

    • Vancouver

      Brioschi TM de LS, Schramm SG, Kano EK, Koono EEM, Ching TH, Serra CH dos R, Porta V. Pharmacokinetics and bioequivalence evaluation of cyclobenzaprine tablets [Internet]. BioMed Research International. 2013 ; 2013 1-6.[citado 2024 maio 21 ] Available from: https://doi.org/10.1155/2013/281392

  • 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

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    • 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: 21 maio 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 maio 21 ]

    • 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 maio 21 ]

  • 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

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    • 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: 21 maio 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 maio 21 ] 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 maio 21 ] Available from: https://doi.org/10.1080/10826076.2011.627607

  • Artigo de periodico

    Biowaiver monographs for immediate release solid oral dosage forms: metronidazole (2011)

    Rediguieri, Camila Fracalossi; Porta, Valentina ; Nunes, Diana S. G; Nunes, Taina M; Junginger, Hans E; Kopp, Sabine; Midha, Kamal K; Shah, Vinod P; Stavchansky, Salomon; Dressman, Jennifer B; Barends, Dirk M

    Source: Journal of Pharmaceutical Science. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, ANTIPROTOZOÁRIOS

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    • ABNT

      REDIGUIERI, Camila Fracalossi et al. Biowaiver monographs for immediate release solid oral dosage forms: metronidazole. Journal of Pharmaceutical Science, v. 100, n. 5, p. 1618-1627, 2011Tradução . . Disponível em: https://doi.org/10.1002/jps.22409. Acesso em: 21 maio 2024.

    • APA

      Rediguieri, C. F., Porta, V., Nunes, D. S. G., Nunes, T. M., Junginger, H. E., Kopp, S., et al. (2011). Biowaiver monographs for immediate release solid oral dosage forms: metronidazole. Journal of Pharmaceutical Science, 100( 5), 1618-1627. doi:10.1002/jps.22409

    • NLM

      Rediguieri CF, Porta V, Nunes DSG, Nunes TM, Junginger HE, Kopp S, Midha KK, Shah VP, Stavchansky S, Dressman JB, Barends DM. Biowaiver monographs for immediate release solid oral dosage forms: metronidazole [Internet]. Journal of Pharmaceutical Science. 2011 ; 100( 5): 1618-1627.[citado 2024 maio 21 ] Available from: https://doi.org/10.1002/jps.22409

    • Vancouver

      Rediguieri CF, Porta V, Nunes DSG, Nunes TM, Junginger HE, Kopp S, Midha KK, Shah VP, Stavchansky S, Dressman JB, Barends DM. Biowaiver monographs for immediate release solid oral dosage forms: metronidazole [Internet]. Journal of Pharmaceutical Science. 2011 ; 100( 5): 1618-1627.[citado 2024 maio 21 ] Available from: https://doi.org/10.1002/jps.22409

  • Artigo de periodico

    Average, population and individual bioequivalence (2010)

    Lopes, Nilcéia; Ruas, K; Serra, Cristina Helena dos Reis ; Porta, Valentina

    Source: SA Pharmaceutical Journal. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, MEDICAMENTO GENÉRICO

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      LOPES, Nilcéia et al. Average, population and individual bioequivalence. SA Pharmaceutical Journal, v. 77, n. 6, p. 46-48, 2010Tradução . . Disponível em: http://www.sapj.co.za/index.php/SAPJ/article/viewFile/539/766. Acesso em: 21 maio 2024.

    • APA

      Lopes, N., Ruas, K., Serra, C. H. dos R., & Porta, V. (2010). Average, population and individual bioequivalence. SA Pharmaceutical Journal, 77( 6), 46-48. Recuperado de http://www.sapj.co.za/index.php/SAPJ/article/viewFile/539/766

    • NLM

      Lopes N, Ruas K, Serra CH dos R, Porta V. Average, population and individual bioequivalence [Internet]. SA Pharmaceutical Journal. 2010 ; 77( 6): 46-48.[citado 2024 maio 21 ] Available from: http://www.sapj.co.za/index.php/SAPJ/article/viewFile/539/766

    • Vancouver

      Lopes N, Ruas K, Serra CH dos R, Porta V. Average, population and individual bioequivalence [Internet]. SA Pharmaceutical Journal. 2010 ; 77( 6): 46-48.[citado 2024 maio 21 ] Available from: http://www.sapj.co.za/index.php/SAPJ/article/viewFile/539/766

  • 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

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    • 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: 21 maio 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 maio 21 ] 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 maio 21 ] 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

  • Artigo de periodico

    Dissolution parameters for sodium diclofenac-containing hypromellose matrix tablet (2010)

    Mourão, Samanta Cardozo; Silva, Cristiane da; Bresolin, Tania M. B; Serra, Cristina Helena dos Reis ; Porta, Valentina

    Source: International Journal of Pharmaceutics. Unidade: FCF

    Subjects: FARMACOCINÉTICA, ANTI-INFLAMATÓRIOS NÃO ESTEROIDES

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      MOURÃO, Samanta Cardozo et al. Dissolution parameters for sodium diclofenac-containing hypromellose matrix tablet. International Journal of Pharmaceutics, v. 386, n. 1-2, p. 201-207, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ijpharm.2009.11.022. Acesso em: 21 maio 2024.

    • APA

      Mourão, S. C., Silva, C. da, Bresolin, T. M. B., Serra, C. H. dos R., & Porta, V. (2010). Dissolution parameters for sodium diclofenac-containing hypromellose matrix tablet. International Journal of Pharmaceutics, 386( 1-2), 201-207. doi:10.1016/j.ijpharm.2009.11.022

    • NLM

      Mourão SC, Silva C da, Bresolin TMB, Serra CH dos R, Porta V. Dissolution parameters for sodium diclofenac-containing hypromellose matrix tablet [Internet]. International Journal of Pharmaceutics. 2010 ; 386( 1-2): 201-207.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ijpharm.2009.11.022

    • Vancouver

      Mourão SC, Silva C da, Bresolin TMB, Serra CH dos R, Porta V. Dissolution parameters for sodium diclofenac-containing hypromellose matrix tablet [Internet]. International Journal of Pharmaceutics. 2010 ; 386( 1-2): 201-207.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ijpharm.2009.11.022

  • Artigo de periodico

    Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma (2009)

    Silva, Marina; Schramm, Simone Grigoleto; Kano, Eunice Kazue; Porta, Valentina ; Serra, Cristina Helena dos Reis

    Source: Journal of Chromatographic Science. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ANTIBIÓTICOS

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    • ABNT

      SILVA, Marina et al. Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science, v. 47, p. 781-784, 2009Tradução . . Acesso em: 21 maio 2024.

    • APA

      Silva, M., Schramm, S. G., Kano, E. K., Porta, V., & Serra, C. H. dos R. (2009). Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science, 47, 781-784.

    • NLM

      Silva M, Schramm SG, Kano EK, Porta V, Serra CH dos R. Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science. 2009 ; 47 781-784.[citado 2024 maio 21 ]

    • Vancouver

      Silva M, Schramm SG, Kano EK, Porta V, Serra CH dos R. Development and validation of a HPLC-MS-MS method for quantification of metronidazole in human plasma. Journal of Chromatographic Science. 2009 ; 47 781-784.[citado 2024 maio 21 ]

  • Artigo de periodico

    Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet (2009)

    Souza, Jacqueline de; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Schramm, Simone Grigoleto; Porta, Valentina ; Storpirtis, Silvia

    Source: Latin American Journal of Pharmacy. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ZIDOVUDINA

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    • ABNT

      SOUZA, Jacqueline de et al. Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet. Latin American Journal of Pharmacy, v. 28, n. 3, p. 433-437, 2009Tradução . . Disponível em: http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf. Acesso em: 21 maio 2024.

    • APA

      Souza, J. de, Kano, E. K., Koono, E. E. M., Schramm, S. G., Porta, V., & Storpirtis, S. (2009). Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet. Latin American Journal of Pharmacy, 28( 3), 433-437. Recuperado de http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf

    • NLM

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet [Internet]. Latin American Journal of Pharmacy. 2009 ; 28( 3): 433-437.[citado 2024 maio 21 ] Available from: http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf

    • Vancouver

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet [Internet]. Latin American Journal of Pharmacy. 2009 ; 28( 3): 433-437.[citado 2024 maio 21 ] Available from: http://www.latamjpharm.org/resumenes/28/3/LAJOP_28_3_1_16.pdf

  • Artigo de periodico

    LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction (2009)

    Souza, Jacqueline de; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Schramm, Simone Grigoleto; Porta, Valentina ; Storpirtis, Silvia

    Source: Chromatographia. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA, EXTRAÇÃO DE LÍQUIDOS, ZIDOVUDINA

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    • ABNT

      SOUZA, Jacqueline de et al. LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia, v. 69, p. S231-S235, 2009Tradução . . Acesso em: 21 maio 2024.

    • APA

      Souza, J. de, Kano, E. K., Koono, E. E. M., Schramm, S. G., Porta, V., & Storpirtis, S. (2009). LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia, 69, S231-S235.

    • NLM

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia. 2009 ; 69 S231-S235.[citado 2024 maio 21 ]

    • Vancouver

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia. 2009 ; 69 S231-S235.[citado 2024 maio 21 ]

  • Artigo de periodico

    Bioequivalence assay between orally disintegrating and conventional tablet formulations in healthy volunteers (2009)

    Armando, Yara Popst; Schramm, Simone Grigoleto; Silva, Marina de Freitas; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Porta, Valentina ; Serra, Cristina Helena dos Reis

    Source: International Journal of Pharmaceutics. Unidade: FCF

    Subjects: FARMACOLOGIA, BIOEQUIVALÊNCIA

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    • ABNT

      ARMANDO, Yara Popst et al. Bioequivalence assay between orally disintegrating and conventional tablet formulations in healthy volunteers. International Journal of Pharmaceutics, v. 366, n. 1-2, p. 149-153, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.ijpharm.2008.09.021. Acesso em: 21 maio 2024.

    • APA

      Armando, Y. P., Schramm, S. G., Silva, M. de F., Kano, E. K., Koono, E. E. M., Porta, V., & Serra, C. H. dos R. (2009). Bioequivalence assay between orally disintegrating and conventional tablet formulations in healthy volunteers. International Journal of Pharmaceutics, 366( 1-2), 149-153. doi:10.1016/j.ijpharm.2008.09.021

    • NLM

      Armando YP, Schramm SG, Silva M de F, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence assay between orally disintegrating and conventional tablet formulations in healthy volunteers [Internet]. International Journal of Pharmaceutics. 2009 ; 366( 1-2): 149-153.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ijpharm.2008.09.021

    • Vancouver

      Armando YP, Schramm SG, Silva M de F, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence assay between orally disintegrating and conventional tablet formulations in healthy volunteers [Internet]. International Journal of Pharmaceutics. 2009 ; 366( 1-2): 149-153.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ijpharm.2008.09.021

  • Artigo de periodico

    HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies (2008)

    Porta, Valentina ; Schramm, Simone Grigoleto; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Armando, Yara Popst; Fukuda, Kazuo; Serra, Cristina Helena dos Reis

    Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: PLASMA, BIOEQUIVALÊNCIA, FARMACOCINÉTICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      PORTA, Valentina et al. HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies. Journal of Pharmaceutical and Biomedical Analysis, v. 46, n. 1, p. 143-147, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2007.10.007. Acesso em: 21 maio 2024.

    • APA

      Porta, V., Schramm, S. G., Kano, E. K., Koono, E. E. M., Armando, Y. P., Fukuda, K., & Serra, C. H. dos R. (2008). HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies. Journal of Pharmaceutical and Biomedical Analysis, 46( 1), 143-147. doi:10.1016/j.jpba.2007.10.007

    • NLM

      Porta V, Schramm SG, Kano EK, Koono EEM, Armando YP, Fukuda K, Serra CH dos R. HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;46( 1): 143-147.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.jpba.2007.10.007

    • Vancouver

      Porta V, Schramm SG, Kano EK, Koono EEM, Armando YP, Fukuda K, Serra CH dos R. HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;46( 1): 143-147.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.jpba.2007.10.007

  • Artigo de periodico

    Pharmacokinetics of tramadol and o-desmethyltramadol in goats after intravenous and oral administration (2008)

    Sousa, Altamir Benedito de; Santos, A. C. D; Schramm, Simone Grigoleto; Porta, Valentina ; Górniak, Silvana Lima; Flório, Jorge Camilo; Spinosa, Helenice de Souza

    Source: Journal of Veterinary Pharmacology Therapeutics. Unidades: FMVZ, FCF

    Subjects: CABRITOS, FARMACOCINÉTICA, FÁRMACOS

    Acesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      SOUSA, Altamir Benedito de et al. Pharmacokinetics of tramadol and o-desmethyltramadol in goats after intravenous and oral administration. Journal of Veterinary Pharmacology Therapeutics, v. 31, n. 1, p. 45-51, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2885.2007.00916.x. Acesso em: 21 maio 2024.

    • APA

      Sousa, A. B. de, Santos, A. C. D., Schramm, S. G., Porta, V., Górniak, S. L., Flório, J. C., & Spinosa, H. de S. (2008). Pharmacokinetics of tramadol and o-desmethyltramadol in goats after intravenous and oral administration. Journal of Veterinary Pharmacology Therapeutics, 31( 1), 45-51. doi:10.1111/j.1365-2885.2007.00916.x

    • NLM

      Sousa AB de, Santos ACD, Schramm SG, Porta V, Górniak SL, Flório JC, Spinosa H de S. Pharmacokinetics of tramadol and o-desmethyltramadol in goats after intravenous and oral administration [Internet]. Journal of Veterinary Pharmacology Therapeutics. 2008 ; 31( 1): 45-51.[citado 2024 maio 21 ] Available from: https://doi.org/10.1111/j.1365-2885.2007.00916.x

    • Vancouver

      Sousa AB de, Santos ACD, Schramm SG, Porta V, Górniak SL, Flório JC, Spinosa H de S. Pharmacokinetics of tramadol and o-desmethyltramadol in goats after intravenous and oral administration [Internet]. Journal of Veterinary Pharmacology Therapeutics. 2008 ; 31( 1): 45-51.[citado 2024 maio 21 ] Available from: https://doi.org/10.1111/j.1365-2885.2007.00916.x

  • Artigo de periodico

    Bioequivalence study of two oral formulations of cefadroxil in healthy volunteers (2008)

    Kano, Eunice Kazue; Porta, Valentina ; Koono, Eunice Emiko Mori; Schramm, Simone Grigoleto; Serra, Cristina Helena dos Reis

    Source: Arzneimittel-Forschung(Drug Research). Unidade: FCF

    Subjects: OBESIDADE, ANTIBIÓTICOS

    How to cite
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    • ABNT

      KANO, Eunice Kazue et al. Bioequivalence study of two oral formulations of cefadroxil in healthy volunteers. Arzneimittel-Forschung(Drug Research), v. 58, n. 1, p. 42-47, 2008Tradução . . Acesso em: 21 maio 2024.

    • APA

      Kano, E. K., Porta, V., Koono, E. E. M., Schramm, S. G., & Serra, C. H. dos R. (2008). Bioequivalence study of two oral formulations of cefadroxil in healthy volunteers. Arzneimittel-Forschung(Drug Research), 58( 1), 42-47.

    • NLM

      Kano EK, Porta V, Koono EEM, Schramm SG, Serra CH dos R. Bioequivalence study of two oral formulations of cefadroxil in healthy volunteers. Arzneimittel-Forschung(Drug Research). 2008 ;58( 1): 42-47.[citado 2024 maio 21 ]

    • Vancouver

      Kano EK, Porta V, Koono EEM, Schramm SG, Serra CH dos R. Bioequivalence study of two oral formulations of cefadroxil in healthy volunteers. Arzneimittel-Forschung(Drug Research). 2008 ;58( 1): 42-47.[citado 2024 maio 21 ]

  • Artigo de periodico

    Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study (2008)

    Serra, Cristina Helena dos Reis ; Koono, Eunice Emiko Mori; Kano, Eunice Kazue; Schramm, Simone Grigoleto; Armando, Yara Popst; Porta, Valentina

    Source: Clinical Therapeutics. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, ZIDOVUDINA (FARMACOCINÉTICA)

    Acesso à fonteDOIHow to cite
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    • ABNT

      SERRA, Cristina Helena dos Reis et al. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study. Clinical Therapeutics, v. 30, n. 5, p. 902-908, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.clinthera.2008.05.003. Acesso em: 21 maio 2024.

    • APA

      Serra, C. H. dos R., Koono, E. E. M., Kano, E. K., Schramm, S. G., Armando, Y. P., & Porta, V. (2008). Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study. Clinical Therapeutics, 30( 5), 902-908. doi:10.1016/j.clinthera.2008.05.003

    • NLM

      Serra CH dos R, Koono EEM, Kano EK, Schramm SG, Armando YP, Porta V. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study [Internet]. Clinical Therapeutics. 2008 ;30( 5): 902-908.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.clinthera.2008.05.003

    • Vancouver

      Serra CH dos R, Koono EEM, Kano EK, Schramm SG, Armando YP, Porta V. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study [Internet]. Clinical Therapeutics. 2008 ;30( 5): 902-908.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.clinthera.2008.05.003

  • Artigo de periodico

    Quantitation of nimesulide in human plasma by high-performance liquid chromatography with ultraviolet absorbance detection and its application to a bioequivalence study (2007)

    Rolim, Clarice Madalena Bueno; Porta, Valentina ; Storpirtis, Silvia

    Source: Arzneimittel-Forschung / Drug Research. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, BIOEQUIVALÊNCIA, ANTI-INFLAMATÓRIOS NÃO ESTEROIDES

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    • ABNT

      ROLIM, Clarice Madalena Bueno e PORTA, Valentina e STORPIRTIS, Silvia. Quantitation of nimesulide in human plasma by high-performance liquid chromatography with ultraviolet absorbance detection and its application to a bioequivalence study. Arzneimittel-Forschung / Drug Research, v. 57, n. 8, p. 537-541, 2007Tradução . . Acesso em: 21 maio 2024.

    • APA

      Rolim, C. M. B., Porta, V., & Storpirtis, S. (2007). Quantitation of nimesulide in human plasma by high-performance liquid chromatography with ultraviolet absorbance detection and its application to a bioequivalence study. Arzneimittel-Forschung / Drug Research, 57( 8), 537-541.

    • NLM

      Rolim CMB, Porta V, Storpirtis S. Quantitation of nimesulide in human plasma by high-performance liquid chromatography with ultraviolet absorbance detection and its application to a bioequivalence study. Arzneimittel-Forschung / Drug Research. 2007 ; 57( 8): 537-541.[citado 2024 maio 21 ]

    • Vancouver

      Rolim CMB, Porta V, Storpirtis S. Quantitation of nimesulide in human plasma by high-performance liquid chromatography with ultraviolet absorbance detection and its application to a bioequivalence study. Arzneimittel-Forschung / Drug Research. 2007 ; 57( 8): 537-541.[citado 2024 maio 21 ]

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