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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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.1016/j.ijpharm.2009.11.022
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.1016/j.ijpharm.2008.09.021
Artigo de periodico
Evaluation of the bioequivalence of capsules containing 150 mg of fluconazole (2005)
Porta, Valentina ; Chang, K. H.; Storpirtis, Silvia
Source: International Journal of Pharmaceutics. Unidade: FCF
Subjects: BIOEQUIVALÊNCIA, CÁPSULAS, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, PLASMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PORTA, Valentina e CHANG, K. H. e STORPIRTIS, Silvia. Evaluation of the bioequivalence of capsules containing 150 mg of fluconazole. International Journal of Pharmaceutics, v. 288, n. 1, p. 81-86, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.ijpharm.2004.09.013. Acesso em: 18 ago. 2024.
APA
Porta, V., Chang, K. H., & Storpirtis, S. (2005). Evaluation of the bioequivalence of capsules containing 150 mg of fluconazole. International Journal of Pharmaceutics, 288( 1), 81-86. doi:10.1016/j.ijpharm.2004.09.013
NLM
Porta V, Chang KH, Storpirtis S. Evaluation of the bioequivalence of capsules containing 150 mg of fluconazole [Internet]. International Journal of Pharmaceutics. 2005 ; 288( 1): 81-86.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1016/j.ijpharm.2004.09.013
Vancouver
Porta V, Chang KH, Storpirtis S. Evaluation of the bioequivalence of capsules containing 150 mg of fluconazole [Internet]. International Journal of Pharmaceutics. 2005 ; 288( 1): 81-86.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1016/j.ijpharm.2004.09.013
Artigo de periodico
Determination of lamivudine in human plasma by HPLC and its use in bioequivalence studies (2005)
Kano, Eunice Kazue; Serra, Cristina Helena dos Reis ; Koono, Eunice Emiko Mori; Andrade, Simone Schramm; Porta, Valentina
Source: International Journal of Pharmaceutics. Unidade: FCF
Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA (MÉTODOS), PLASMA, BIOEQUIVALÊNCIA (ESTUDO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.1016/j.ijpharm.2005.03.002

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