Filtros : "FCF-FBF" "Journal of Pharmaceutical and Biomedical Analysis" Removidos: "Semana Farmacêutica de Ciência e Tecnologia" "REVISAO DE TRADUCAO" Limpar

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

    Subjects: INDÚSTRIA FARMACÊUTICA, CROMATOGRAFIA LÍQUIDA

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      PASSARIN, Paula Beatriz Silva e LOURENÇO, Felipe Rebello. Enhancing analytical development in the pharmaceutical industry: a DoE-QSRR model for virtual method operable design region assessment. Journal of Pharmaceutical and Biomedical Analysis, v. 239, p. 1-12, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/j.jpba.2023.115907. Acesso em: 23 jun. 2024.
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      Passarin, P. B. S., & Lourenço, F. R. (2024). Enhancing analytical development in the pharmaceutical industry: a DoE-QSRR model for virtual method operable design region assessment. Journal of Pharmaceutical and Biomedical Analysis, 239, 1-12. doi:10.1016/j.jpba.2023.115907
    • NLM

      Passarin PBS, Lourenço FR. Enhancing analytical development in the pharmaceutical industry: a DoE-QSRR model for virtual method operable design region assessment [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2024 ; 239 1-12.[citado 2024 jun. 23 ] Available from: https://dx.doi.org/10.1016/j.jpba.2023.115907
    • Vancouver

      Passarin PBS, Lourenço FR. Enhancing analytical development in the pharmaceutical industry: a DoE-QSRR model for virtual method operable design region assessment [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2024 ; 239 1-12.[citado 2024 jun. 23 ] Available from: https://dx.doi.org/10.1016/j.jpba.2023.115907
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: MEDICAMENTO, MÉTODO DE MONTE CARLO, MEDIÇÃO DE RISCO

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      MARTINS, Maisa Torres e LOURENÇO, Felipe Rebello. Measurement uncertainty for < 905 > Uniformity of Dosage Units tests using Monte Carlo and bootstrapping methods – Uncertainties arising from sampling and analytical steps. Journal of Pharmaceutical and Biomedical Analysis, v. 238, p. 1-8 art. 115857, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/j.jpba.2023.115857. Acesso em: 23 jun. 2024.
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      Martins, M. T., & Lourenço, F. R. (2024). Measurement uncertainty for < 905 > Uniformity of Dosage Units tests using Monte Carlo and bootstrapping methods – Uncertainties arising from sampling and analytical steps. Journal of Pharmaceutical and Biomedical Analysis, 238, 1-8 art. 115857. doi:10.1016/j.jpba.2023.115857
    • NLM

      Martins MT, Lourenço FR. Measurement uncertainty for < 905 > Uniformity of Dosage Units tests using Monte Carlo and bootstrapping methods – Uncertainties arising from sampling and analytical steps [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2024 ; 238 1-8 art. 115857.[citado 2024 jun. 23 ] Available from: https://dx.doi.org/10.1016/j.jpba.2023.115857
    • Vancouver

      Martins MT, Lourenço FR. Measurement uncertainty for < 905 > Uniformity of Dosage Units tests using Monte Carlo and bootstrapping methods – Uncertainties arising from sampling and analytical steps [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2024 ; 238 1-8 art. 115857.[citado 2024 jun. 23 ] Available from: https://dx.doi.org/10.1016/j.jpba.2023.115857
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, MÉTODO DE MONTE CARLO, FÁRMACOS (SISTEMA REPRODUTOR)

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      SILVA, Fernando Antunes da e LOURENÇO, Felipe Rebello e CALIXTO, Leandro Augusto. Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach. Journal of Pharmaceutical and Biomedical Analysis, v. 225, p. 1-14 art. 115208, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2022.115208. Acesso em: 23 jun. 2024.
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      Silva, F. A. da, Lourenço, F. R., & Calixto, L. A. (2023). Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach. Journal of Pharmaceutical and Biomedical Analysis, 225, 1-14 art. 115208. doi:10.1016/j.jpba.2022.115208
    • NLM

      Silva FA da, Lourenço FR, Calixto LA. Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 225 1-14 art. 115208.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2022.115208
    • Vancouver

      Silva FA da, Lourenço FR, Calixto LA. Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 225 1-14 art. 115208.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2022.115208
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: MEDICAMENTO, MEDIÇÃO DE RISCO, ANÁLISE MULTIVARIADA

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      SILVA, Cintia Margueiro da e LOURENÇO, Felipe Rebello. Definition of multivariate acceptance limits (guard-bands) applied to pharmaceutical equivalence assessment. Journal of Pharmaceutical and Biomedical Analysis, v. 222, p. 1-7 art. 115080, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2022.115080. Acesso em: 23 jun. 2024.
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      Silva, C. M. da, & Lourenço, F. R. (2023). Definition of multivariate acceptance limits (guard-bands) applied to pharmaceutical equivalence assessment. Journal of Pharmaceutical and Biomedical Analysis, 222, 1-7 art. 115080. doi:10.1016/j.jpba.2022.115080
    • NLM

      Silva CM da, Lourenço FR. Definition of multivariate acceptance limits (guard-bands) applied to pharmaceutical equivalence assessment [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 222 1-7 art. 115080.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2022.115080
    • Vancouver

      Silva CM da, Lourenço FR. Definition of multivariate acceptance limits (guard-bands) applied to pharmaceutical equivalence assessment [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 222 1-7 art. 115080.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2022.115080
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: MEDICAMENTO, MEDIÇÃO DE RISCO, BIOEQUIVALÊNCIA, QUALIDADE DOS MEDICAMENTOS

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      BERTANHA, Maria Luiza de Godoy e LOURENÇO, Felipe Rebello. Risk of false pharmaceutical equivalence (non-equivalence) decisions due to measurement uncertainty. Journal of Pharmaceutical and Biomedical Analysis, v. 204, p. 1-9 art. 114269, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2021.114269. Acesso em: 23 jun. 2024.
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      Bertanha, M. L. de G., & Lourenço, F. R. (2021). Risk of false pharmaceutical equivalence (non-equivalence) decisions due to measurement uncertainty. Journal of Pharmaceutical and Biomedical Analysis, 204, 1-9 art. 114269. doi:10.1016/j.jpba.2021.114269
    • NLM

      Bertanha ML de G, Lourenço FR. Risk of false pharmaceutical equivalence (non-equivalence) decisions due to measurement uncertainty [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2021 ; 204 1-9 art. 114269.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2021.114269
    • Vancouver

      Bertanha ML de G, Lourenço FR. Risk of false pharmaceutical equivalence (non-equivalence) decisions due to measurement uncertainty [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2021 ; 204 1-9 art. 114269.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2021.114269
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Assunto: CROMATOGRAFIA LÍQUIDA

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      SEPAROVIC, Luciana e LOURENÇO, Felipe Rebello. Frequentist approach for estimation of false decision risks in conformity assessment based on measurement uncertainty of liquid chromatography analytical procedures. Journal of Pharmaceutical and Biomedical Analysis, v. 184, p. 1-7 art. 113203, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2020.113203. Acesso em: 23 jun. 2024.
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      Separovic, L., & Lourenço, F. R. (2020). Frequentist approach for estimation of false decision risks in conformity assessment based on measurement uncertainty of liquid chromatography analytical procedures. Journal of Pharmaceutical and Biomedical Analysis, 184, 1-7 art. 113203. doi:10.1016/j.jpba.2020.113203
    • NLM

      Separovic L, Lourenço FR. Frequentist approach for estimation of false decision risks in conformity assessment based on measurement uncertainty of liquid chromatography analytical procedures [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2020 ; 184 1-7 art. 113203.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2020.113203
    • Vancouver

      Separovic L, Lourenço FR. Frequentist approach for estimation of false decision risks in conformity assessment based on measurement uncertainty of liquid chromatography analytical procedures [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2020 ; 184 1-7 art. 113203.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2020.113203
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA, MÉTODO DE MONTE CARLO

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      SEPAROVIC, Luciana e LOURENÇO, Felipe Rebello. Measurement uncertainty and risk of false conformity decision in the performance evaluation of liquid chromatography analytical procedures. Journal of Pharmaceutical and Biomedical Analysis, v. 171, p. 73-80, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2019.04.005. Acesso em: 23 jun. 2024.
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      Separovic, L., & Lourenço, F. R. (2019). Measurement uncertainty and risk of false conformity decision in the performance evaluation of liquid chromatography analytical procedures. Journal of Pharmaceutical and Biomedical Analysis, 171, 73-80. doi:10.1016/j.jpba.2019.04.005
    • NLM

      Separovic L, Lourenço FR. Measurement uncertainty and risk of false conformity decision in the performance evaluation of liquid chromatography analytical procedures [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2019 ; 171 73-80.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2019.04.005
    • Vancouver

      Separovic L, Lourenço FR. Measurement uncertainty and risk of false conformity decision in the performance evaluation of liquid chromatography analytical procedures [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2019 ; 171 73-80.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2019.04.005
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FCF, FFCLRP

    Subjects: TERAPIA FOTODINÂMICA, NANOPARTÍCULAS, FLUORESCÊNCIA, CROMATOGRAFIA LÍQUIDA, FARMACOCINÉTICA

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      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: 23 jun. 2024.
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      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 jun. 23 ] 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 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2011.04.016
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: PLASMA, BIOEQUIVALÊNCIA, FARMACOCINÉTICA

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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: 23 jun. 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 jun. 23 ] 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 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2007.10.007
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, DOENÇA DE CHAGAS

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      GRILLO, Renato et al. Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin. Journal of Pharmaceutical and Biomedical Analysis, v. 47, n. 2, p. 295-302, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2008.01.010. Acesso em: 23 jun. 2024.
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      Grillo, R., Melo, N. F. S. de, Moraes, C. M., Lima, R. de, Menezes, C. M. de S., Ferreira, E. I., et al. (2008). Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin. Journal of Pharmaceutical and Biomedical Analysis, 47( 2), 295-302. doi:10.1016/j.jpba.2008.01.010
    • NLM

      Grillo R, Melo NFS de, Moraes CM, Lima R de, Menezes CM de S, Ferreira EI, Rosa AH, Fraceto LF. Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;47( 2): 295-302.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2008.01.010
    • Vancouver

      Grillo R, Melo NFS de, Moraes CM, Lima R de, Menezes CM de S, Ferreira EI, Rosa AH, Fraceto LF. Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;47( 2): 295-302.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2008.01.010
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA, FÁRMACOS IMUNOSSUPRESSORES

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      FÁZIO, Tatiana Tatit de et al. Quantitative determination and sampling of azathioprine residues for cleaning validation in production area. Journal of Pharmaceutical and Biomedical Analysis, v. 43, n. 4, p. 1495-1498, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2006.10.016. Acesso em: 23 jun. 2024.
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      Fázio, T. T. de, Singh, A. K., Kedor-Hackmann, E. R. M., & Santoro, M. I. R. M. (2007). Quantitative determination and sampling of azathioprine residues for cleaning validation in production area. Journal of Pharmaceutical and Biomedical Analysis, 43( 4), 1495-1498. doi:10.1016/j.jpba.2006.10.016
    • NLM

      Fázio TT de, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Quantitative determination and sampling of azathioprine residues for cleaning validation in production area [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2007 ; 43( 4): 1495-1498.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2006.10.016
    • Vancouver

      Fázio TT de, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Quantitative determination and sampling of azathioprine residues for cleaning validation in production area [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2007 ; 43( 4): 1495-1498.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2006.10.016
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FCF, IQ

    Subjects: ELETROFORESE CAPILAR DE ZONA, COSMÉTICOS

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      DUTRA, Elizângela Abreu et al. Determination of 'alpha'-hydroxy acids in cosmetic products by capillary electrophoresis. Journal of Pharmaceutical and Biomedical Analysis, v. 40, n. 2, p. 242-248, 2006Tradução . . Acesso em: 23 jun. 2024.
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      Dutra, E. A., Santoro, M. I. R. M., Micke, G. A., Tavares, M. F. M., & Kedor-Hackmann, E. R. M. (2006). Determination of 'alpha'-hydroxy acids in cosmetic products by capillary electrophoresis. Journal of Pharmaceutical and Biomedical Analysis, 40( 2), 242-248.
    • NLM

      Dutra EA, Santoro MIRM, Micke GA, Tavares MFM, Kedor-Hackmann ERM. Determination of 'alpha'-hydroxy acids in cosmetic products by capillary electrophoresis. Journal of Pharmaceutical and Biomedical Analysis. 2006 ; 40( 2): 242-248.[citado 2024 jun. 23 ]
    • Vancouver

      Dutra EA, Santoro MIRM, Micke GA, Tavares MFM, Kedor-Hackmann ERM. Determination of 'alpha'-hydroxy acids in cosmetic products by capillary electrophoresis. Journal of Pharmaceutical and Biomedical Analysis. 2006 ; 40( 2): 242-248.[citado 2024 jun. 23 ]
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ANTIBIÓTICOS (QUANTIFICAÇÃO;DETERMINAÇÃO), FARMACOLOGIA

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      SANTORO, Maria Inês Rocha Miritello et al. Quantitative determination of gatifloxacin, levofloxacin, lomefloxacin and pefloxacin fluoroquinolonic antibiotics in pharmaceutical preparations by high-performance liquid chromatography. Journal of Pharmaceutical and Biomedical Analysis, v. 40, n. 1, p. 179-184, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2005.06.018. Acesso em: 23 jun. 2024.
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      Santoro, M. I. R. M., Kassab, N. M., Singh, A. K., & Kedor-Hackmann, E. R. M. (2006). Quantitative determination of gatifloxacin, levofloxacin, lomefloxacin and pefloxacin fluoroquinolonic antibiotics in pharmaceutical preparations by high-performance liquid chromatography. Journal of Pharmaceutical and Biomedical Analysis, 40( 1), 179-184. doi:10.1016/j.jpba.2005.06.018
    • NLM

      Santoro MIRM, Kassab NM, Singh AK, Kedor-Hackmann ERM. Quantitative determination of gatifloxacin, levofloxacin, lomefloxacin and pefloxacin fluoroquinolonic antibiotics in pharmaceutical preparations by high-performance liquid chromatography [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2006 ; 40( 1): 179-184.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2005.06.018
    • Vancouver

      Santoro MIRM, Kassab NM, Singh AK, Kedor-Hackmann ERM. Quantitative determination of gatifloxacin, levofloxacin, lomefloxacin and pefloxacin fluoroquinolonic antibiotics in pharmaceutical preparations by high-performance liquid chromatography [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2006 ; 40( 1): 179-184.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2005.06.018
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: COSMÉTICOS, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, GEL (FORMAS FARMACÊUTICAS) (PREPARO), CREME (PREPARO)

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      GARCIA, Pedro López et al. Development and validation of a HPLC and a UV derivative spectrophotometric methods for determination of hydroquinone in gel and cream preparations. Journal of Pharmaceutical and Biomedical Analysis, v. 39, n. 3-4, p. 764-768, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2005.04.016. Acesso em: 23 jun. 2024.
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      Garcia, P. L., Santoro, M. I. R. M., Kedor-Hackmann, E. R. M., & Singh, A. K. (2005). Development and validation of a HPLC and a UV derivative spectrophotometric methods for determination of hydroquinone in gel and cream preparations. Journal of Pharmaceutical and Biomedical Analysis, 39( 3-4), 764-768. doi:10.1016/j.jpba.2005.04.016
    • NLM

      Garcia PL, Santoro MIRM, Kedor-Hackmann ERM, Singh AK. Development and validation of a HPLC and a UV derivative spectrophotometric methods for determination of hydroquinone in gel and cream preparations [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2005 ; 39( 3-4): 764-768.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2005.04.016
    • Vancouver

      Garcia PL, Santoro MIRM, Kedor-Hackmann ERM, Singh AK. Development and validation of a HPLC and a UV derivative spectrophotometric methods for determination of hydroquinone in gel and cream preparations [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2005 ; 39( 3-4): 764-768.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2005.04.016
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: IQ, FCF

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ELETROFORESE (MÉTODO DE SEPARAÇÃO) (COMPARAÇÃO), FORMAS FARMACÊUTICAS

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      AURORA-PRADO, Maria Segunda et al. Comparison of capillary electrophoresis and reversed-phase liquid chromatography methodologies for determination of diazepam in pharmaceutical tablets. Journal of Pharmaceutical and Biomedical Analysis, v. 37, n. 2, p. 273-279, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2004.10.026. Acesso em: 23 jun. 2024.
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      Aurora-Prado, M. S., Steppe, M., Tavares, M. F. M., Kedor-Hackmann, E. R. M., & Santoro, M. I. R. M. (2005). Comparison of capillary electrophoresis and reversed-phase liquid chromatography methodologies for determination of diazepam in pharmaceutical tablets. Journal of Pharmaceutical and Biomedical Analysis, 37( 2), 273-279. doi:10.1016/j.jpba.2004.10.026
    • NLM

      Aurora-Prado MS, Steppe M, Tavares MFM, Kedor-Hackmann ERM, Santoro MIRM. Comparison of capillary electrophoresis and reversed-phase liquid chromatography methodologies for determination of diazepam in pharmaceutical tablets [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2005 ; 37( 2): 273-279.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2004.10.026
    • Vancouver

      Aurora-Prado MS, Steppe M, Tavares MFM, Kedor-Hackmann ERM, Santoro MIRM. Comparison of capillary electrophoresis and reversed-phase liquid chromatography methodologies for determination of diazepam in pharmaceutical tablets [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2005 ; 37( 2): 273-279.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/j.jpba.2004.10.026
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FCF, IQ

    Subjects: ELETROFORESE CAPILAR DE ZONA (MÉTODOS), HIV (TERAPIA), FARMACOLOGIA

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      AURORA-PRADO, Maria Segunda et al. Capillary electrophoretic method for determination of protease inhibitor indinavir sulfate used in human immunodeficiency virus therapy. Journal of Pharmaceutical and Biomedical Analysis, v. 34, n. 2, p. 441-450, 2004Tradução . . Disponível em: https://doi.org/10.1016/s0731-7085(03)00530-2. Acesso em: 23 jun. 2024.
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      Aurora-Prado, M. S., Kedor-Hackmann, E. R. M., Santoro, M. I. R. M., Pinto, T. de J. A., & Tavares, M. F. M. (2004). Capillary electrophoretic method for determination of protease inhibitor indinavir sulfate used in human immunodeficiency virus therapy. Journal of Pharmaceutical and Biomedical Analysis, 34( 2), 441-450. doi:10.1016/s0731-7085(03)00530-2
    • NLM

      Aurora-Prado MS, Kedor-Hackmann ERM, Santoro MIRM, Pinto T de JA, Tavares MFM. Capillary electrophoretic method for determination of protease inhibitor indinavir sulfate used in human immunodeficiency virus therapy [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2004 ; 34( 2): 441-450.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/s0731-7085(03)00530-2
    • Vancouver

      Aurora-Prado MS, Kedor-Hackmann ERM, Santoro MIRM, Pinto T de JA, Tavares MFM. Capillary electrophoretic method for determination of protease inhibitor indinavir sulfate used in human immunodeficiency virus therapy [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2004 ; 34( 2): 441-450.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/s0731-7085(03)00530-2
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: IQ, FCF

    Subjects: ELETROQUÍMICA, QUÍMICA FARMACÊUTICA, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, DNA (INTERAÇÃO)

    Acesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      GIL, Eric de Souza et al. Electrochemical evaluation of rhodium dimer-DNA interactions. Journal of Pharmaceutical and Biomedical Analysis, v. 29, n. 4, p. 579-584, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0731-7085(01)00700-2. Acesso em: 23 jun. 2024.
    • APA

      Gil, E. de S., Serrano, S. H. P., Ferreira, E. I., & Kubota, L. T. (2002). Electrochemical evaluation of rhodium dimer-DNA interactions. Journal of Pharmaceutical and Biomedical Analysis, 29( 4), 579-584. doi:10.1016/s0731-7085(01)00700-2
    • NLM

      Gil E de S, Serrano SHP, Ferreira EI, Kubota LT. Electrochemical evaluation of rhodium dimer-DNA interactions [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2002 ; 29( 4): 579-584.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/s0731-7085(01)00700-2
    • Vancouver

      Gil E de S, Serrano SHP, Ferreira EI, Kubota LT. Electrochemical evaluation of rhodium dimer-DNA interactions [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2002 ; 29( 4): 579-584.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/s0731-7085(01)00700-2
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: IQ, FCF

    Subjects: ELETROQUÍMICA, BIOQUÍMICA, QUÍMICA FARMACÊUTICA, DNA

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      LA-SCALEA, Mauro Aquiles et al. Voltammetric behavior of benzonidazole at a DNA-electrochemical biosensor. Journal of Pharmaceutical and Biomedical Analysis, v. 29, n. 3, p. 561-568, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0731-7085(02)00081-x. Acesso em: 23 jun. 2024.
    • APA

      La-Scalea, M. A., Serrano, S. H. P., Ferreira, E. I., & Brett, A. M. O. (2002). Voltammetric behavior of benzonidazole at a DNA-electrochemical biosensor. Journal of Pharmaceutical and Biomedical Analysis, 29( 3), 561-568. doi:10.1016/s0731-7085(02)00081-x
    • NLM

      La-Scalea MA, Serrano SHP, Ferreira EI, Brett AMO. Voltammetric behavior of benzonidazole at a DNA-electrochemical biosensor [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2002 ; 29( 3): 561-568.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/s0731-7085(02)00081-x
    • Vancouver

      La-Scalea MA, Serrano SHP, Ferreira EI, Brett AMO. Voltammetric behavior of benzonidazole at a DNA-electrochemical biosensor [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2002 ; 29( 3): 561-568.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1016/s0731-7085(02)00081-x

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