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  • Source: International Journal of Pharmaceutics. Unidade: FCF

    Subjects: FARMACOLOGIA, BIOEQUIVALÊNCIA

    Acesso à fonteDOIHow to cite
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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: 13 set. 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 set. 13 ] 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 set. 13 ] Available from: https://doi.org/10.1016/j.ijpharm.2008.09.021
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: PLASMA, BIOEQUIVALÊNCIA, FARMACOCINÉTICA

    Acesso à fonteDOIHow to cite
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      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: 13 set. 2024.
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      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 set. 13 ] 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 set. 13 ] Available from: https://doi.org/10.1016/j.jpba.2007.10.007
  • Source: International Journal of Pharmaceutics. Unidade: FCF

    Subjects: EMULSÕES (FORMAS FARMACÊUTICAS), TECNOLOGIA FARMACÊUTICA

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      BABY, André Rolim et al. Emulsified systems based on glyceryl monostearate and potassium cetyl phosphate: scale-up and characterization of physical properties. International Journal of Pharmaceutics, v. 361, n. 1-2, p. 99-103, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.ijpharm.2008.05.029. Acesso em: 13 set. 2024.
    • APA

      Baby, A. R., Santoro, D. M., Velasco, M. V. R., & Serra, C. H. dos R. (2008). Emulsified systems based on glyceryl monostearate and potassium cetyl phosphate: scale-up and characterization of physical properties. International Journal of Pharmaceutics, 361( 1-2), 99-103. doi:10.1016/j.ijpharm.2008.05.029
    • NLM

      Baby AR, Santoro DM, Velasco MVR, Serra CH dos R. Emulsified systems based on glyceryl monostearate and potassium cetyl phosphate: scale-up and characterization of physical properties [Internet]. International Journal of Pharmaceutics. 2008 ; 361( 1-2): 99-103.[citado 2024 set. 13 ] Available from: https://doi.org/10.1016/j.ijpharm.2008.05.029
    • Vancouver

      Baby AR, Santoro DM, Velasco MVR, Serra CH dos R. Emulsified systems based on glyceryl monostearate and potassium cetyl phosphate: scale-up and characterization of physical properties [Internet]. International Journal of Pharmaceutics. 2008 ; 361( 1-2): 99-103.[citado 2024 set. 13 ] Available from: https://doi.org/10.1016/j.ijpharm.2008.05.029
  • Source: Clinical Therapeutics. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, ZIDOVUDINA (FARMACOCINÉTICA)

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      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: 13 set. 2024.
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      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 set. 13 ] 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 set. 13 ] Available from: https://doi.org/10.1016/j.clinthera.2008.05.003
  • Source: International Journal of Pharmaceutics. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA (MÉTODOS), PLASMA, BIOEQUIVALÊNCIA (ESTUDO)

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      KANO, Eunice Kazue et al. Determination of lamivudine in human plasma by HPLC and its use in bioequivalence studies. International Journal of Pharmaceutics, v. 297, n. 1-2, p. 73-79, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.ijpharm.2005.03.002. Acesso em: 13 set. 2024.
    • APA

      Kano, E. K., Serra, C. H. dos R., Koono, E. E. M., Andrade, S. S., & Porta, V. (2005). Determination of lamivudine in human plasma by HPLC and its use in bioequivalence studies. International Journal of Pharmaceutics, 297( 1-2), 73-79. doi:10.1016/j.ijpharm.2005.03.002
    • NLM

      Kano EK, Serra CH dos R, Koono EEM, Andrade SS, Porta V. Determination of lamivudine in human plasma by HPLC and its use in bioequivalence studies [Internet]. International Journal of Pharmaceutics. 2005 ; 297( 1-2): 73-79.[citado 2024 set. 13 ] Available from: https://doi.org/10.1016/j.ijpharm.2005.03.002
    • Vancouver

      Kano EK, Serra CH dos R, Koono EEM, Andrade SS, Porta V. Determination of lamivudine in human plasma by HPLC and its use in bioequivalence studies [Internet]. International Journal of Pharmaceutics. 2005 ; 297( 1-2): 73-79.[citado 2024 set. 13 ] Available from: https://doi.org/10.1016/j.ijpharm.2005.03.002

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