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

    Subjects: INDÚSTRIA FARMACÊUTICA, COMPRIMIDOS, MEDIÇÃO DE RISCO, MÉTODO DE MONTE CARLO

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      SANTOS, Monique Silva dos et al. Analytical quality by design and measurement uncertainty in the development of discriminative dissolution method for pediatric fixed-dose combination dispersible tablets of isoniazid and rifampicin. Journal of Pharmaceutical and Biomedical Analysis, v. 265, p. 1-11 art. 116994, 2025Tradução . . Disponível em: https://dx.doi.org/10.1016/j.jpba.2025.116994. Acesso em: 29 nov. 2025.
    • APA

      Santos, M. S. dos, Nascimento, D. D. do, Medeiros, J. J. S., Lourenço, F. R., Oliveira, C. A. de, & Prado, L. D. (2025). Analytical quality by design and measurement uncertainty in the development of discriminative dissolution method for pediatric fixed-dose combination dispersible tablets of isoniazid and rifampicin. Journal of Pharmaceutical and Biomedical Analysis, 265, 1-11 art. 116994. doi:10.1016/j.jpba.2025.116994
    • NLM

      Santos MS dos, Nascimento DD do, Medeiros JJS, Lourenço FR, Oliveira CA de, Prado LD. Analytical quality by design and measurement uncertainty in the development of discriminative dissolution method for pediatric fixed-dose combination dispersible tablets of isoniazid and rifampicin [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2025 ; 265 1-11 art. 116994.[citado 2025 nov. 29 ] Available from: https://dx.doi.org/10.1016/j.jpba.2025.116994
    • Vancouver

      Santos MS dos, Nascimento DD do, Medeiros JJS, Lourenço FR, Oliveira CA de, Prado LD. Analytical quality by design and measurement uncertainty in the development of discriminative dissolution method for pediatric fixed-dose combination dispersible tablets of isoniazid and rifampicin [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2025 ; 265 1-11 art. 116994.[citado 2025 nov. 29 ] Available from: https://dx.doi.org/10.1016/j.jpba.2025.116994
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: ALBUMINAS, IMUNOGLOBULINAS, FARMACOPEIAS

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      TANPIPAT, Amornrid et al. An efficient and reliable determination of hyaluronidase supports revision of the United States Pharmacopeia USP46-NF41 monograph – Hyaluronidase for injection. Journal of Pharmaceutical and Biomedical Analysis, v. 265, p. 1-16 art. 117032, 2025Tradução . . Disponível em: https://dx.doi.org/10.1016/j.jpba.2025.117032. Acesso em: 29 nov. 2025.
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      Tanpipat, A., Breyer, C. A., Fernandes, R. B., Gomes, M. V., Silva, L. M., Parsons, R. B., et al. (2025). An efficient and reliable determination of hyaluronidase supports revision of the United States Pharmacopeia USP46-NF41 monograph – Hyaluronidase for injection. Journal of Pharmaceutical and Biomedical Analysis, 265, 1-16 art. 117032. doi:10.1016/j.jpba.2025.117032
    • NLM

      Tanpipat A, Breyer CA, Fernandes RB, Gomes MV, Silva LM, Parsons RB, Pessoa Junior A, Long PF. An efficient and reliable determination of hyaluronidase supports revision of the United States Pharmacopeia USP46-NF41 monograph – Hyaluronidase for injection [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2025 ; 265 1-16 art. 117032.[citado 2025 nov. 29 ] Available from: https://dx.doi.org/10.1016/j.jpba.2025.117032
    • Vancouver

      Tanpipat A, Breyer CA, Fernandes RB, Gomes MV, Silva LM, Parsons RB, Pessoa Junior A, Long PF. An efficient and reliable determination of hyaluronidase supports revision of the United States Pharmacopeia USP46-NF41 monograph – Hyaluronidase for injection [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2025 ; 265 1-16 art. 117032.[citado 2025 nov. 29 ] Available from: https://dx.doi.org/10.1016/j.jpba.2025.117032
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: FÁRMACOS, ANTI-INFLAMATÓRIOS, MEDIÇÃO DE RISCO

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      CRIVILARI, Victória Aparecida Vit e SANTOS, Jean Bispo dos e LOURENÇO, Felipe Rebello. Impact of sample heterogeneity on the evaluation of uncertainty from sampling and analytical steps in pharmaceutical analysis. Journal of Pharmaceutical and Biomedical Analysis, v. 255, p. 1-7 art. 116660, 2025Tradução . . Disponível em: https://dx.doi.org/10.1016/j.jpba.2025.116660. Acesso em: 29 nov. 2025.
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      Crivilari, V. A. V., Santos, J. B. dos, & Lourenço, F. R. (2025). Impact of sample heterogeneity on the evaluation of uncertainty from sampling and analytical steps in pharmaceutical analysis. Journal of Pharmaceutical and Biomedical Analysis, 255, 1-7 art. 116660. doi:10.1016/j.jpba.2025.116660
    • NLM

      Crivilari VAV, Santos JB dos, Lourenço FR. Impact of sample heterogeneity on the evaluation of uncertainty from sampling and analytical steps in pharmaceutical analysis [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2025 ; 255 1-7 art. 116660.[citado 2025 nov. 29 ] Available from: https://dx.doi.org/10.1016/j.jpba.2025.116660
    • Vancouver

      Crivilari VAV, Santos JB dos, Lourenço FR. Impact of sample heterogeneity on the evaluation of uncertainty from sampling and analytical steps in pharmaceutical analysis [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2025 ; 255 1-7 art. 116660.[citado 2025 nov. 29 ] Available from: https://dx.doi.org/10.1016/j.jpba.2025.116660
  • 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: 29 nov. 2025.
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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 2025 nov. 29 ] 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 2025 nov. 29 ] 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: 29 nov. 2025.
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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 2025 nov. 29 ] 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 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2022.115208
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: CANABINOIDES, PLASMA

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      FABRIS, André Luis et al. A new application of the switchable hydrophilicity solvent-based homogenous liquid–liquid microextraction to analyze synthetic cannabinoids in plasma by LC-MS/MS. Journal of Pharmaceutical and Biomedical Analysis, v. 234, p. 1-11 art. 115588, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2023.115588. Acesso em: 29 nov. 2025.
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      Fabris, A. L., Martins, A. F., Costa, J. L., & Yonamine, M. (2023). A new application of the switchable hydrophilicity solvent-based homogenous liquid–liquid microextraction to analyze synthetic cannabinoids in plasma by LC-MS/MS. Journal of Pharmaceutical and Biomedical Analysis, 234, 1-11 art. 115588. doi:10.1016/j.jpba.2023.115588
    • NLM

      Fabris AL, Martins AF, Costa JL, Yonamine M. A new application of the switchable hydrophilicity solvent-based homogenous liquid–liquid microextraction to analyze synthetic cannabinoids in plasma by LC-MS/MS [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 234 1-11 art. 115588.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2023.115588
    • Vancouver

      Fabris AL, Martins AF, Costa JL, Yonamine M. A new application of the switchable hydrophilicity solvent-based homogenous liquid–liquid microextraction to analyze synthetic cannabinoids in plasma by LC-MS/MS [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 234 1-11 art. 115588.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2023.115588
  • 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: 29 nov. 2025.
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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 2025 nov. 29 ] 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 2025 nov. 29 ] 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: 29 nov. 2025.
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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 2025 nov. 29 ] 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 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2021.114269
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: IQ

    Subjects: CROMATOGRAFIA LÍQUIDA, QUIMIOMETRIA, MÉTODO DE MONTE CARLO

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      ABREU, Juliana Caldeira e MAHR, Amanda Guiraldelli e LAGO, Claudimir Lucio do. Stability-indicating method development for quantification of bromopride, its impurities, and degradation products by ultra-high performance liquid chromatography applying Analytical Quality by Design principles. Journal of Pharmaceutical and Biomedical Analysis, v. 205, p. 1-9 art. 114306, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2021.114306. Acesso em: 29 nov. 2025.
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      Abreu, J. C., Mahr, A. G., & Lago, C. L. do. (2021). Stability-indicating method development for quantification of bromopride, its impurities, and degradation products by ultra-high performance liquid chromatography applying Analytical Quality by Design principles. Journal of Pharmaceutical and Biomedical Analysis, 205, 1-9 art. 114306. doi:10.1016/j.jpba.2021.114306
    • NLM

      Abreu JC, Mahr AG, Lago CL do. Stability-indicating method development for quantification of bromopride, its impurities, and degradation products by ultra-high performance liquid chromatography applying Analytical Quality by Design principles [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2021 ; 205 1-9 art. 114306.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2021.114306
    • Vancouver

      Abreu JC, Mahr AG, Lago CL do. Stability-indicating method development for quantification of bromopride, its impurities, and degradation products by ultra-high performance liquid chromatography applying Analytical Quality by Design principles [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2021 ; 205 1-9 art. 114306.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2021.114306
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: ESALQ

    Subjects: ANTIDEPRESSIVOS, ELETROANÁLISE, ELETRODO, VOLTAMETRIA

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      MARTINS, Fernanda C. O. L e PIMENTA, Laura C e SOUZA, Djenaine de. Antidepressants determination using an electroanalytical approach: a review of methods. Journal of Pharmaceutical and Biomedical Analysis, v. 206, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2021.114365. Acesso em: 29 nov. 2025.
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      Martins, F. C. O. L., Pimenta, L. C., & Souza, D. de. (2021). Antidepressants determination using an electroanalytical approach: a review of methods. Journal of Pharmaceutical and Biomedical Analysis, 206. doi:10.1016/j.jpba.2021.114365
    • NLM

      Martins FCOL, Pimenta LC, Souza D de. Antidepressants determination using an electroanalytical approach: a review of methods [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2021 ; 206[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2021.114365
    • Vancouver

      Martins FCOL, Pimenta LC, Souza D de. Antidepressants determination using an electroanalytical approach: a review of methods [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2021 ; 206[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2021.114365
  • 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: 29 nov. 2025.
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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 2025 nov. 29 ] 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 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2020.113203
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FMRP, FCFRP

    Subjects: FÁRMACOS, ANTIRRETROVIRAIS, GRAVIDEZ

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      MOREIRA, Fernanda de Lima et al. Determination of raltegravir and raltegravir glucuronide in human plasma and urine by LC-MS/MS with application in a maternal-fetal pharmacokinetic study. Journal of Pharmaceutical and Biomedical Analysis, v. 177, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2019.112838. Acesso em: 29 nov. 2025.
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      Moreira, F. de L., Marques, M. P., Duarte, G., & Lanchote, V. L. (2020). Determination of raltegravir and raltegravir glucuronide in human plasma and urine by LC-MS/MS with application in a maternal-fetal pharmacokinetic study. Journal of Pharmaceutical and Biomedical Analysis, 177. doi:10.1016/j.jpba.2019.112838
    • NLM

      Moreira F de L, Marques MP, Duarte G, Lanchote VL. Determination of raltegravir and raltegravir glucuronide in human plasma and urine by LC-MS/MS with application in a maternal-fetal pharmacokinetic study [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2020 ; 177[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2019.112838
    • Vancouver

      Moreira F de L, Marques MP, Duarte G, Lanchote VL. Determination of raltegravir and raltegravir glucuronide in human plasma and urine by LC-MS/MS with application in a maternal-fetal pharmacokinetic study [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2020 ; 177[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2019.112838
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FMRP, FCFRP

    Assunto: ANTIDEPRESSIVOS

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      SOUZA, Marília Cristina Oliveira et al. Analysis of bupivacaine enantiomers in plasma as total and unbound concentrations using LC-MS/MS:: application in a pharmacokinetic study of a parturient with placental transfer. Journal of Pharmaceutical and Biomedical Analysis, v. 164, p. 268-275, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2018.10.040. Acesso em: 29 nov. 2025.
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      Souza, M. C. O., Marques, M. P., Duarte, G., & Lanchote, V. L. (2019). Analysis of bupivacaine enantiomers in plasma as total and unbound concentrations using LC-MS/MS:: application in a pharmacokinetic study of a parturient with placental transfer. Journal of Pharmaceutical and Biomedical Analysis, 164, 268-275. doi:10.1016/j.jpba.2018.10.040
    • NLM

      Souza MCO, Marques MP, Duarte G, Lanchote VL. Analysis of bupivacaine enantiomers in plasma as total and unbound concentrations using LC-MS/MS:: application in a pharmacokinetic study of a parturient with placental transfer [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2019 ; 164 268-275.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.10.040
    • Vancouver

      Souza MCO, Marques MP, Duarte G, Lanchote VL. Analysis of bupivacaine enantiomers in plasma as total and unbound concentrations using LC-MS/MS:: application in a pharmacokinetic study of a parturient with placental transfer [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2019 ; 164 268-275.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.10.040
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FCFRP, FMRP

    Subjects: CROMATOGRAFIA LÍQUIDA, ESPECTROMETRIA DE MASSAS

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      CUSINATO, Diego Alberto Ciscato et al. LC-MS/MS analysis of the plasma concentrations of a cocktail of 5 cytochrome P450 and P-glycoprotein probe substrates and their metabolites using subtherapeutic doses. Journal of Pharmaceutical and Biomedical Analysis, v. 164, p. 430-441, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2018.10.029. Acesso em: 29 nov. 2025.
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      Cusinato, D. A. C., Filgueira, G. C. de O., Rocha, A., Cintra, M. A. de C. T., Lanchote, V. L., & Coelho, E. B. (2019). LC-MS/MS analysis of the plasma concentrations of a cocktail of 5 cytochrome P450 and P-glycoprotein probe substrates and their metabolites using subtherapeutic doses. Journal of Pharmaceutical and Biomedical Analysis, 164, 430-441. doi:10.1016/j.jpba.2018.10.029
    • NLM

      Cusinato DAC, Filgueira GC de O, Rocha A, Cintra MA de CT, Lanchote VL, Coelho EB. LC-MS/MS analysis of the plasma concentrations of a cocktail of 5 cytochrome P450 and P-glycoprotein probe substrates and their metabolites using subtherapeutic doses [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2019 ; 164 430-441.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.10.029
    • Vancouver

      Cusinato DAC, Filgueira GC de O, Rocha A, Cintra MA de CT, Lanchote VL, Coelho EB. LC-MS/MS analysis of the plasma concentrations of a cocktail of 5 cytochrome P450 and P-glycoprotein probe substrates and their metabolites using subtherapeutic doses [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2019 ; 164 430-441.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.10.029
  • 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: 29 nov. 2025.
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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 2025 nov. 29 ] 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 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2019.04.005
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FFCLRP

    Subjects: PESTICIDAS, FUNGICIDAS, METABOLISMO

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      ALBUQUERQUE, Nayara Cristina Perez de et al. Metabolism studies of chiral pesticides: a critical review. Journal of Pharmaceutical and Biomedical Analysis, v. 147, p. 89-109, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2017.08.011. Acesso em: 29 nov. 2025.
    • APA

      Albuquerque, N. C. P. de, Carrão, D. B., Habenschus, M. D., & Oliveira, A. R. M. de. (2018). Metabolism studies of chiral pesticides: a critical review. Journal of Pharmaceutical and Biomedical Analysis, 147, 89-109. doi:10.1016/j.jpba.2017.08.011
    • NLM

      Albuquerque NCP de, Carrão DB, Habenschus MD, Oliveira ARM de. Metabolism studies of chiral pesticides: a critical review [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 147 89-109.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2017.08.011
    • Vancouver

      Albuquerque NCP de, Carrão DB, Habenschus MD, Oliveira ARM de. Metabolism studies of chiral pesticides: a critical review [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 147 89-109.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2017.08.011
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FFCLRP

    Subjects: EXTRATOS (FORMAS FARMACÊUTICAS), CROMATOGRAFIA LÍQUIDA

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    • ABNT

      VANZOLINI, K. L. et al. Acetylcholinesterase affinity-based screening assay on Lippia gracilis Schauer extracts. Journal of Pharmaceutical and Biomedical Analysis, v. 153, p. 232-237, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2018.02.035. Acesso em: 29 nov. 2025.
    • APA

      Vanzolini, K. L., Sprenger, R. da F., Leme, G. M., Moraes, V. R. de S., Vilela, A. F. L., Cardoso, C. L., & Cass, Q. B. (2018). Acetylcholinesterase affinity-based screening assay on Lippia gracilis Schauer extracts. Journal of Pharmaceutical and Biomedical Analysis, 153, 232-237. doi:10.1016/j.jpba.2018.02.035
    • NLM

      Vanzolini KL, Sprenger R da F, Leme GM, Moraes VR de S, Vilela AFL, Cardoso CL, Cass QB. Acetylcholinesterase affinity-based screening assay on Lippia gracilis Schauer extracts [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 153 232-237.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.02.035
    • Vancouver

      Vanzolini KL, Sprenger R da F, Leme GM, Moraes VR de S, Vilela AFL, Cardoso CL, Cass QB. Acetylcholinesterase affinity-based screening assay on Lippia gracilis Schauer extracts [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 153 232-237.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.02.035
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCFRP

    Subjects: INIBIDORES DE ENZIMAS, CROMATOGRAFIA LÍQUIDA DE ALTA PRESSÃO, AVALIAÇÃO DE MEDICAMENTOS, REPRODUTIBILIDADE DE RESULTADOS

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    • ABNT

      CORNELIO, Vivian Estevam et al. Cathepsin D immobilized capillary reactors for on-flow screening assays. Journal of Pharmaceutical and Biomedical Analysis, v. 151, p. 252-259, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2018.01.001. Acesso em: 29 nov. 2025.
    • APA

      Cornelio, V. E., Moraes, M. C. de, Domingues, V. de C., Fernandes, J. B., Silva, M. F. das G. F. da, Cass, Q. B., & Vieira, P. C. (2018). Cathepsin D immobilized capillary reactors for on-flow screening assays. Journal of Pharmaceutical and Biomedical Analysis, 151, 252-259. doi:10.1016/j.jpba.2018.01.001
    • NLM

      Cornelio VE, Moraes MC de, Domingues V de C, Fernandes JB, Silva MF das GF da, Cass QB, Vieira PC. Cathepsin D immobilized capillary reactors for on-flow screening assays [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 151 252-259.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.01.001
    • Vancouver

      Cornelio VE, Moraes MC de, Domingues V de C, Fernandes JB, Silva MF das GF da, Cass QB, Vieira PC. Cathepsin D immobilized capillary reactors for on-flow screening assays [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 151 252-259.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2018.01.001
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidades: FMRP, FCFRP

    Subjects: ANTICONVULSIVANTES, FARMACOCINÉTICA, ESPECTROMETRIA DE MASSAS

    Acesso à fonteDOIHow to cite
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    • ABNT

      ANTUNES, Natalícia de Jesus et al. Analysis of unbound plasma concentration of oxcarbazepine and the 10-hydroxycarbazepine enantiomers by liquid chromatography with tandem mass spectrometry in healthy volunteers. Journal of Pharmaceutical and Biomedical Analysis, v. 149, p. 442-447, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2017.11.041. Acesso em: 29 nov. 2025.
    • APA

      Antunes, N. de J., Wichert-Ana, L., Coelho, E. B., Della Pasqua, O., Alexandre Júnior, V., Takayanagui, O. M., et al. (2018). Analysis of unbound plasma concentration of oxcarbazepine and the 10-hydroxycarbazepine enantiomers by liquid chromatography with tandem mass spectrometry in healthy volunteers. Journal of Pharmaceutical and Biomedical Analysis, 149, 442-447. doi:10.1016/j.jpba.2017.11.041
    • NLM

      Antunes N de J, Wichert-Ana L, Coelho EB, Della Pasqua O, Alexandre Júnior V, Takayanagui OM, Marques MP, Lanchote VL. Analysis of unbound plasma concentration of oxcarbazepine and the 10-hydroxycarbazepine enantiomers by liquid chromatography with tandem mass spectrometry in healthy volunteers [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 149 442-447.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2017.11.041
    • Vancouver

      Antunes N de J, Wichert-Ana L, Coelho EB, Della Pasqua O, Alexandre Júnior V, Takayanagui OM, Marques MP, Lanchote VL. Analysis of unbound plasma concentration of oxcarbazepine and the 10-hydroxycarbazepine enantiomers by liquid chromatography with tandem mass spectrometry in healthy volunteers [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 149 442-447.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2017.11.041
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FMRP

    Subjects: LEITE MATERNO, CROMATOGRAFIA LÍQUIDA

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    • ABNT

      LOPES, Bianca Rebelo et al. Simultaneous quantification of fluoxetine and norfluoxetine in colostrum and mature human milk using a 2-dimensional liquid chromatography–tandem mass spectrometry system. Journal of Pharmaceutical and Biomedical Analysis, v. 150, p. 362-367, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2017.12.041. Acesso em: 29 nov. 2025.
    • APA

      Lopes, B. R., Cassiano, N. M., Carvalho, D. M., Moisés, E. C. D., & Cass, Q. B. (2018). Simultaneous quantification of fluoxetine and norfluoxetine in colostrum and mature human milk using a 2-dimensional liquid chromatography–tandem mass spectrometry system. Journal of Pharmaceutical and Biomedical Analysis, 150, 362-367. doi:10.1016/j.jpba.2017.12.041
    • NLM

      Lopes BR, Cassiano NM, Carvalho DM, Moisés ECD, Cass QB. Simultaneous quantification of fluoxetine and norfluoxetine in colostrum and mature human milk using a 2-dimensional liquid chromatography–tandem mass spectrometry system [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 150 362-367.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2017.12.041
    • Vancouver

      Lopes BR, Cassiano NM, Carvalho DM, Moisés ECD, Cass QB. Simultaneous quantification of fluoxetine and norfluoxetine in colostrum and mature human milk using a 2-dimensional liquid chromatography–tandem mass spectrometry system [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2018 ; 150 362-367.[citado 2025 nov. 29 ] Available from: https://doi.org/10.1016/j.jpba.2017.12.041

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