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  • Source: Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: FÁRMACOS, MÉTODO DE MONTE CARLO, BIODISPONIBILIDADE

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      BEZZON, Vinícius Danilo Nonato et al. Describing the influence of ball-milling on the amorphization of flubendazole using the PDF and RMC methods with X-ray powder diffraction data. Journal of Pharmaceutical Sciences, 2022Tradução . . Disponível em: https://dx.doi.org/10.1016/j.xphs.2022.06.018. Acesso em: 08 ago. 2022.
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      Bezzon, V. D. N., Pinto, R. da S., Araujo, G. L. B. de, Lima, J. C. de, & Ferreira, F. F. (2022). Describing the influence of ball-milling on the amorphization of flubendazole using the PDF and RMC methods with X-ray powder diffraction data. Journal of Pharmaceutical Sciences. doi:10.1016/j.xphs.2022.06.018
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      Bezzon VDN, Pinto R da S, Araujo GLB de, Lima JC de, Ferreira FF. Describing the influence of ball-milling on the amorphization of flubendazole using the PDF and RMC methods with X-ray powder diffraction data [Internet]. Journal of Pharmaceutical Sciences. 2022 ;[citado 2022 ago. 08 ] Available from: https://dx.doi.org/10.1016/j.xphs.2022.06.018
    • Vancouver

      Bezzon VDN, Pinto R da S, Araujo GLB de, Lima JC de, Ferreira FF. Describing the influence of ball-milling on the amorphization of flubendazole using the PDF and RMC methods with X-ray powder diffraction data [Internet]. Journal of Pharmaceutical Sciences. 2022 ;[citado 2022 ago. 08 ] Available from: https://dx.doi.org/10.1016/j.xphs.2022.06.018
  • Source: Journal of Pharmaceutical Sciences. Unidades: FCF, IQ

    Subjects: LIGANTES, MEDICAMENTO, FARMACOCINÉTICA

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      GONZAGA, Rodrigo Vieira et al. Perspectives about self-immolative drug delivery systems. Journal of Pharmaceutical Sciences, v. 109, p. 3262-3281, 2020Tradução . . Disponível em: http://dx.doi.org/10.1016/j.xphs.2020.08.014. Acesso em: 08 ago. 2022.
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      Gonzaga, R. V., Nascimento, L. A. do, Santos, S. da S., Sanches, B. M. A., Giarolla, J., & Ferreira, E. I. (2020). Perspectives about self-immolative drug delivery systems. Journal of Pharmaceutical Sciences, 109, 3262-3281. doi:10.1016/j.xphs.2020.08.014
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      Gonzaga RV, Nascimento LA do, Santos S da S, Sanches BMA, Giarolla J, Ferreira EI. Perspectives about self-immolative drug delivery systems [Internet]. Journal of Pharmaceutical Sciences. 2020 ; 109 3262-3281.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2020.08.014
    • Vancouver

      Gonzaga RV, Nascimento LA do, Santos S da S, Sanches BMA, Giarolla J, Ferreira EI. Perspectives about self-immolative drug delivery systems [Internet]. Journal of Pharmaceutical Sciences. 2020 ; 109 3262-3281.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2020.08.014
  • Source: Journal of Pharmaceutical Sciences. Unidade: FCFRP

    Subjects: MUCOSA ORAL, ANESTÉSICOS LOCAIS, FÁRMACOS

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      SERPE, Luciano et al. Full-thickness intraoral mucosa barrier models for in vitro drug-permeation studies using microneedles. Journal of Pharmaceutical Sciences, v. 108, n. 5, p. 1756-1764, 2019Tradução . . Disponível em: http://dx.doi.org/10.1016/j.xphs.2018.12.004. Acesso em: 08 ago. 2022.
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      Serpe, L., Muniz, B. V., Santos, C. P. dos, Silva, C. B. da, Volpato, M. C., Groppo, F. C., et al. (2019). Full-thickness intraoral mucosa barrier models for in vitro drug-permeation studies using microneedles. Journal of Pharmaceutical Sciences, 108( 5), 1756-1764. doi:10.1016/j.xphs.2018.12.004
    • NLM

      Serpe L, Muniz BV, Santos CP dos, Silva CB da, Volpato MC, Groppo FC, Lopez RFV, Franz-Montan M. Full-thickness intraoral mucosa barrier models for in vitro drug-permeation studies using microneedles [Internet]. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1756-1764.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2018.12.004
    • Vancouver

      Serpe L, Muniz BV, Santos CP dos, Silva CB da, Volpato MC, Groppo FC, Lopez RFV, Franz-Montan M. Full-thickness intraoral mucosa barrier models for in vitro drug-permeation studies using microneedles [Internet]. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1756-1764.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2018.12.004
  • Source: Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, SOLUBILIDADE

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      COMPRI, Jéssica de Cássia Zaghi et al. Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences, v. 108, n. 5, p. 1848-1856, 2019Tradução . . Acesso em: 08 ago. 2022.
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      Compri, J. de C. Z., Felli, V. M. A., Lourenço, F. R., Takatsuka, T., Fotaki, N., Löbenberg, R., et al. (2019). Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences, 108( 5), 1848-1856. doi:10.1016/j.xphs.2018.12.015
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      Compri J de CZ, Felli VMA, Lourenço FR, Takatsuka T, Fotaki N, Löbenberg R, Bou-Chacra NA, Araujo GLB de. Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1848-1856.[citado 2022 ago. 08 ]
    • Vancouver

      Compri J de CZ, Felli VMA, Lourenço FR, Takatsuka T, Fotaki N, Löbenberg R, Bou-Chacra NA, Araujo GLB de. Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1848-1856.[citado 2022 ago. 08 ]
  • Source: Journal of Pharmaceutical Sciences. Unidades: IF, FCFRP

    Subjects: PELE, ANTI-INFLAMATÓRIOS, NEOPLASIAS CUTÂNEAS

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      DANTE, Mariane de Cássia Lima et al. Liquid crystalline systems based on glyceryl monooleate and penetration enhancers for skin delivery of celecoxib: characterization, in vitro drug release, and in vivo studies. Journal of Pharmaceutical Sciences, v. 107, n. 3, p. 870-878, 2018Tradução . . Disponível em: http://dx.doi.org/10.1016/j.xphs.2017.10.039. Acesso em: 08 ago. 2022.
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      Dante, M. de C. L., Cardoso, L. N. B., Fantini, M. C. de A., Praça, F. S. G., Medina, W. S. G., Pierre, M. B. R., & Lara, M. G. (2018). Liquid crystalline systems based on glyceryl monooleate and penetration enhancers for skin delivery of celecoxib: characterization, in vitro drug release, and in vivo studies. Journal of Pharmaceutical Sciences, 107( 3), 870-878. doi:10.1016/j.xphs.2017.10.039
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      Dante M de CL, Cardoso LNB, Fantini MC de A, Praça FSG, Medina WSG, Pierre MBR, Lara MG. Liquid crystalline systems based on glyceryl monooleate and penetration enhancers for skin delivery of celecoxib: characterization, in vitro drug release, and in vivo studies [Internet]. Journal of Pharmaceutical Sciences. 2018 ; 107( 3): 870-878.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2017.10.039
    • Vancouver

      Dante M de CL, Cardoso LNB, Fantini MC de A, Praça FSG, Medina WSG, Pierre MBR, Lara MG. Liquid crystalline systems based on glyceryl monooleate and penetration enhancers for skin delivery of celecoxib: characterization, in vitro drug release, and in vivo studies [Internet]. Journal of Pharmaceutical Sciences. 2018 ; 107( 3): 870-878.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2017.10.039
  • Source: Journal of Pharmaceutical Sciences. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, FILARIOSE, ESPECTROSCOPIA RAMAN

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      HONORATO, Sara B. et al. On the thermal stability of the diethylcarbamazine-fortified table salt used in the control of lymphatic filariasis. Journal of Pharmaceutical Sciences, v. 105, n. 8, p. 2437-2443, 2016Tradução . . Disponível em: http://dx.doi.org/10.1016/j.xphs.2016.06.003. Acesso em: 08 ago. 2022.
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      Honorato, S. B., Mendonça, J. S., Boechat, N., Ellena, J., Ayala, A. P., Silva, C. C. P., & Oliveira, Y. S. (2016). On the thermal stability of the diethylcarbamazine-fortified table salt used in the control of lymphatic filariasis. Journal of Pharmaceutical Sciences, 105( 8), 2437-2443. doi:10.1016/j.xphs.2016.06.003
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      Honorato SB, Mendonça JS, Boechat N, Ellena J, Ayala AP, Silva CCP, Oliveira YS. On the thermal stability of the diethylcarbamazine-fortified table salt used in the control of lymphatic filariasis [Internet]. Journal of Pharmaceutical Sciences. 2016 ; 105( 8): 2437-2443.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2016.06.003
    • Vancouver

      Honorato SB, Mendonça JS, Boechat N, Ellena J, Ayala AP, Silva CCP, Oliveira YS. On the thermal stability of the diethylcarbamazine-fortified table salt used in the control of lymphatic filariasis [Internet]. Journal of Pharmaceutical Sciences. 2016 ; 105( 8): 2437-2443.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2016.06.003
  • Source: Journal of Pharmaceutical Sciences. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, POLIMORFISMO, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      SOUSA, Eduardo Gomes Rodrigues de et al. Solution and solid state nuclear magnetic resonance spectroscopic characterization of efavirenz. Journal of Pharmaceutical Sciences, v. 105, n. 9, p. 2656-2664, 2016Tradução . . Disponível em: http://dx.doi.org/10.1016/j.xphs.2015.10.006. Acesso em: 08 ago. 2022.
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      Sousa, E. G. R. de, Carvalho, E. M. de, Gil, R. A. da S. S., Santos, T. C. dos, Borré, L. B., Santos Filho, O. A., & Ellena, J. (2016). Solution and solid state nuclear magnetic resonance spectroscopic characterization of efavirenz. Journal of Pharmaceutical Sciences, 105( 9), 2656-2664. doi:10.1016/j.xphs.2015.10.006
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      Sousa EGR de, Carvalho EM de, Gil RA da SS, Santos TC dos, Borré LB, Santos Filho OA, Ellena J. Solution and solid state nuclear magnetic resonance spectroscopic characterization of efavirenz [Internet]. Journal of Pharmaceutical Sciences. 2016 ; 105( 9): 2656-2664.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2015.10.006
    • Vancouver

      Sousa EGR de, Carvalho EM de, Gil RA da SS, Santos TC dos, Borré LB, Santos Filho OA, Ellena J. Solution and solid state nuclear magnetic resonance spectroscopic characterization of efavirenz [Internet]. Journal of Pharmaceutical Sciences. 2016 ; 105( 9): 2656-2664.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1016/j.xphs.2015.10.006
  • Source: Journal of Pharmaceutical Sciences. Unidade: FZEA

    Subjects: FILMES COMESTÍVEIS (PRODUÇÃO), COLÁGENO, PRÓPOLIS, FÁRMACOS, MODELOS MATEMÁTICOS, CINÉTICA

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      BORGES, Josiane Gonçalves e CARVALHO, Rosemary Aparecida de. Orally disintegrating films containing propolis: properties and release profile. Journal of Pharmaceutical Sciences, v. 104, n. 4, p. 1431-1439, 2015Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.24355. Acesso em: 08 ago. 2022.
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      Borges, J. G., & Carvalho, R. A. de. (2015). Orally disintegrating films containing propolis: properties and release profile. Journal of Pharmaceutical Sciences, 104( 4), 1431-1439. doi:10.1002/jps.24355
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      Borges JG, Carvalho RA de. Orally disintegrating films containing propolis: properties and release profile [Internet]. Journal of Pharmaceutical Sciences. 2015 ; 104( 4): 1431-1439.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.24355
    • Vancouver

      Borges JG, Carvalho RA de. Orally disintegrating films containing propolis: properties and release profile [Internet]. Journal of Pharmaceutical Sciences. 2015 ; 104( 4): 1431-1439.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.24355
  • Source: Journal of Pharmaceutical Sciences. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, ESTADO SÓLIDO, ANÁLISE TÉRMICA, SOLUBILIDADE

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      RUSSO, Marcos G. et al. Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine. Journal of Pharmaceutical Sciences, v. No 2014, n. 11, p. 3754-3763, 2014Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.24196. Acesso em: 08 ago. 2022.
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      Russo, M. G., Brusau, E. V., Ellena, J., & Narda, G. E. (2014). Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine. Journal of Pharmaceutical Sciences, No 2014( 11), 3754-3763. doi:10.1002/jps.24196
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      Russo MG, Brusau EV, Ellena J, Narda GE. Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine [Internet]. Journal of Pharmaceutical Sciences. 2014 ; No 2014( 11): 3754-3763.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.24196
    • Vancouver

      Russo MG, Brusau EV, Ellena J, Narda GE. Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine [Internet]. Journal of Pharmaceutical Sciences. 2014 ; No 2014( 11): 3754-3763.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.24196
  • Source: Journal of Pharmaceutical Sciences. Unidade: EP

    Subjects: NANOTECNOLOGIA, PRATA, NANOPARTÍCULAS

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      SANTOS, Carolina Alves dos et al. Silver nanoparticles: therapeutical uses, toxicity, and safety issues. Journal of Pharmaceutical Sciences, v. 103, n. 7, p. 1931-1944, 2014Tradução . . Disponível em: https://doi.org/10.1002/jps.24001. Acesso em: 08 ago. 2022.
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      Santos, C. A. dos, Ingle, A. P., Gupta, I., Galdiero, S., Galdiero, M., Gade, A., et al. (2014). Silver nanoparticles: therapeutical uses, toxicity, and safety issues. Journal of Pharmaceutical Sciences, 103( 7), 1931-1944. doi:10.1002/jps.24001
    • NLM

      Santos CA dos, Ingle AP, Gupta I, Galdiero S, Galdiero M, Gade A, Rai M, Seckler MM. Silver nanoparticles: therapeutical uses, toxicity, and safety issues [Internet]. Journal of Pharmaceutical Sciences. 2014 ; 103( 7): 1931-1944.[citado 2022 ago. 08 ] Available from: https://doi.org/10.1002/jps.24001
    • Vancouver

      Santos CA dos, Ingle AP, Gupta I, Galdiero S, Galdiero M, Gade A, Rai M, Seckler MM. Silver nanoparticles: therapeutical uses, toxicity, and safety issues [Internet]. Journal of Pharmaceutical Sciences. 2014 ; 103( 7): 1931-1944.[citado 2022 ago. 08 ] Available from: https://doi.org/10.1002/jps.24001
  • Source: Journal of Pharmaceutical Sciences. Unidade: ICB

    Subjects: FARMACOLOGIA, ANTIOXIDANTES

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      THOMAS, Siji et al. Stability, cutaneous delivery, and antioxidant potential of a lipoic acid and α-tocopherol codrug incorporated in microemulsions. Journal of Pharmaceutical Sciences, v. 103, n. 8, p. 2530-2538, 2014Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.24053. Acesso em: 08 ago. 2022.
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      Thomas, S., Vieira, C. S., Hass, M. A., & Lopes, L. B. (2014). Stability, cutaneous delivery, and antioxidant potential of a lipoic acid and α-tocopherol codrug incorporated in microemulsions. Journal of Pharmaceutical Sciences, 103( 8), 2530-2538. doi:10.1002/jps.24053
    • NLM

      Thomas S, Vieira CS, Hass MA, Lopes LB. Stability, cutaneous delivery, and antioxidant potential of a lipoic acid and α-tocopherol codrug incorporated in microemulsions [Internet]. Journal of Pharmaceutical Sciences. 2014 ; 103( 8): 2530-2538.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.24053
    • Vancouver

      Thomas S, Vieira CS, Hass MA, Lopes LB. Stability, cutaneous delivery, and antioxidant potential of a lipoic acid and α-tocopherol codrug incorporated in microemulsions [Internet]. Journal of Pharmaceutical Sciences. 2014 ; 103( 8): 2530-2538.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.24053
  • Source: Journal of Pharmaceutical Sciences. Unidades: IME, FCF

    Subjects: BIOEQUIVALÊNCIA, SOLUBILIDADE

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      CRISTOFOLETTI, Rodrigo et al. A comparative analysis of biopharmaceutics classification system and biopharmaceutics drug disposition classification system: a cross-sectional survey with 500 bioequivalence studies. Journal of Pharmaceutical Sciences, v. 102, n. 9, p. 3136-3144, 2013Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.23515. Acesso em: 08 ago. 2022.
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      Cristofoletti, R., Chiann, C., Dressman, J. B., & Storpirtis, S. (2013). A comparative analysis of biopharmaceutics classification system and biopharmaceutics drug disposition classification system: a cross-sectional survey with 500 bioequivalence studies. Journal of Pharmaceutical Sciences, 102( 9), 3136-3144. doi:10.1002/jps.23515
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      Cristofoletti R, Chiann C, Dressman JB, Storpirtis S. A comparative analysis of biopharmaceutics classification system and biopharmaceutics drug disposition classification system: a cross-sectional survey with 500 bioequivalence studies [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 9): 3136-3144.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23515
    • Vancouver

      Cristofoletti R, Chiann C, Dressman JB, Storpirtis S. A comparative analysis of biopharmaceutics classification system and biopharmaceutics drug disposition classification system: a cross-sectional survey with 500 bioequivalence studies [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 9): 3136-3144.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23515
  • Source: Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: ZIDOVUDINA, SOLUBILIDADE, BIODISPONIBILIDADE, BIOEQUIVALÊNCIA

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      SOARES, Kelen C. C et al. Biowaiver monographs for immediate-release solid oral dosage forms: Zidovudine (azidothymidine). Journal of Pharmaceutical Sciences, v. 102, n. 8, p. 2409-2423, 2013Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.23624. Acesso em: 08 ago. 2022.
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      Soares, K. C. C., Rediguieri, C. F., Souza, J. de, Serra, C. H. dos R., Abrahamsson, B., Groot, D. W., et al. (2013). Biowaiver monographs for immediate-release solid oral dosage forms: Zidovudine (azidothymidine). Journal of Pharmaceutical Sciences, 102( 8), 2409-2423. doi:10.1002/jps.23624
    • NLM

      Soares KCC, Rediguieri CF, Souza J de, Serra CH dos R, Abrahamsson B, Groot DW, Kopp S, Langguth P, Polli JE, Shah VP, Dressman J. Biowaiver monographs for immediate-release solid oral dosage forms: Zidovudine (azidothymidine) [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 8): 2409-2423.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23624
    • Vancouver

      Soares KCC, Rediguieri CF, Souza J de, Serra CH dos R, Abrahamsson B, Groot DW, Kopp S, Langguth P, Polli JE, Shah VP, Dressman J. Biowaiver monographs for immediate-release solid oral dosage forms: Zidovudine (azidothymidine) [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 8): 2409-2423.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23624
  • Source: Journal of Pharmaceutical Sciences. Unidade: IFSC

    Subjects: ESPECTROSCOPIA RAMAN, POLIMORFISMO, CRISTALOGRAFIA

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      PAULA, Karina de et al. Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs. Journal of Pharmaceutical Sciences, v. 102, n. 10, p. 3528-3538, 2013Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.23658. Acesso em: 08 ago. 2022.
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      Paula, K. de, Camí, G. E., Brusau, E. V., Narda, G. E., & Ellena, J. (2013). Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs. Journal of Pharmaceutical Sciences, 102( 10), 3528-3538. doi:10.1002/jps.23658
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      Paula K de, Camí GE, Brusau EV, Narda GE, Ellena J. Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 10): 3528-3538.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23658
    • Vancouver

      Paula K de, Camí GE, Brusau EV, Narda GE, Ellena J. Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 10): 3528-3538.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23658
  • Source: Journal of Pharmaceutical Sciences. Unidade: EP

    Subjects: PLASMÍDEOS, GENES, DNA, TRANSFECÇÃO

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      LA VEGA, Jonathan de et al. Impact of plasmid quality on lipoplex-mediated transfection. Journal of Pharmaceutical Sciences, v. 102, n. 11, p. 3932-3941, 2013Tradução . . Disponível em: https://doi.org/10.1002/jps.23709. Acesso em: 08 ago. 2022.
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      La Vega, J. de, Braak, B. T., Azzoni, A. R., Monteiro, G. A., & Prazeres, D. M. F. P. (2013). Impact of plasmid quality on lipoplex-mediated transfection. Journal of Pharmaceutical Sciences, 102( 11), 3932-3941. doi:10.1002/jps.23709
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      La Vega J de, Braak BT, Azzoni AR, Monteiro GA, Prazeres DMFP. Impact of plasmid quality on lipoplex-mediated transfection [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 11): 3932-3941.[citado 2022 ago. 08 ] Available from: https://doi.org/10.1002/jps.23709
    • Vancouver

      La Vega J de, Braak BT, Azzoni AR, Monteiro GA, Prazeres DMFP. Impact of plasmid quality on lipoplex-mediated transfection [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 11): 3932-3941.[citado 2022 ago. 08 ] Available from: https://doi.org/10.1002/jps.23709
  • Source: Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: ABSORÇÃO, FORMAS FARMACÊUTICAS, SOLUBILIDADE

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      SILVA, Arthur L. L et al. Biowaiver monographs for immediate-release solid oral dosage forms: stavudine. Journal of Pharmaceutical Sciences, v. 101, n. 1, p. 10-16, 2012Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.22756. Acesso em: 08 ago. 2022.
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      Silva, A. L. L., Cristofoletti, R., Storpirtis, S., Sousa, V. D., Junginger, H. E., Shah, V. P., et al. (2012). Biowaiver monographs for immediate-release solid oral dosage forms: stavudine. Journal of Pharmaceutical Sciences, 101( 1), 10-16. doi:10.1002/jps.22756
    • NLM

      Silva ALL, Cristofoletti R, Storpirtis S, Sousa VD, Junginger HE, Shah VP, Stavchansky S, Dressman JB, Barends DM. Biowaiver monographs for immediate-release solid oral dosage forms: stavudine [Internet]. Journal of Pharmaceutical Sciences. 2012 ; 101( 1): 10-16.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.22756
    • Vancouver

      Silva ALL, Cristofoletti R, Storpirtis S, Sousa VD, Junginger HE, Shah VP, Stavchansky S, Dressman JB, Barends DM. Biowaiver monographs for immediate-release solid oral dosage forms: stavudine [Internet]. Journal of Pharmaceutical Sciences. 2012 ; 101( 1): 10-16.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.22756
  • Source: Journal of Pharmaceutical Sciences. Unidade: IQ

    Subjects: NANOTECNOLOGIA, NANOPARTÍCULAS, COSMÉTICOS

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    • ABNT

      PAULA, Leonardo Rodrigues de et al. Evaluation of sun protection factor of cosmetic formulations by a simple visual in vitro method mimicking the in vivo method. Journal of Pharmaceutical Sciences, v. 101, n. 2, p. 726-732, 2012Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.22797. Acesso em: 08 ago. 2022.
    • APA

      Paula, L. R. de, Parússulo, A. L. A., Araki, K., & Toma, H. E. (2012). Evaluation of sun protection factor of cosmetic formulations by a simple visual in vitro method mimicking the in vivo method. Journal of Pharmaceutical Sciences, 101( 2), 726-732. doi:10.1002/jps.22797
    • NLM

      Paula LR de, Parússulo ALA, Araki K, Toma HE. Evaluation of sun protection factor of cosmetic formulations by a simple visual in vitro method mimicking the in vivo method [Internet]. Journal of Pharmaceutical Sciences. 2012 ; 101( 2): 726-732.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.22797
    • Vancouver

      Paula LR de, Parússulo ALA, Araki K, Toma HE. Evaluation of sun protection factor of cosmetic formulations by a simple visual in vitro method mimicking the in vivo method [Internet]. Journal of Pharmaceutical Sciences. 2012 ; 101( 2): 726-732.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.22797
  • Source: Journal of Pharmaceutical Sciences. Unidade: IFSC

    Subjects: FÁRMACOS (DESENVOLVIMENTO), DIFRAÇÃO POR RAIOS X, POLIMORFISMO

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    • ABNT

      MARTINS, Felipe T. et al. Lamivudine salts with improved solubilities. Journal of Pharmaceutical Sciences, v. 101, n. 6, p. 2143-2154, 2012Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.23117. Acesso em: 08 ago. 2022.
    • APA

      Martins, F. T., Bonfilio, R., Araújo, M. B., & Ellena, J. (2012). Lamivudine salts with improved solubilities. Journal of Pharmaceutical Sciences, 101( 6), 2143-2154. doi:10.1002/jps.23117
    • NLM

      Martins FT, Bonfilio R, Araújo MB, Ellena J. Lamivudine salts with improved solubilities [Internet]. Journal of Pharmaceutical Sciences. 2012 ; 101( 6): 2143-2154.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23117
    • Vancouver

      Martins FT, Bonfilio R, Araújo MB, Ellena J. Lamivudine salts with improved solubilities [Internet]. Journal of Pharmaceutical Sciences. 2012 ; 101( 6): 2143-2154.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.23117
  • Source: Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: NANOTECNOLOGIA, INTERAÇÃO DE MEDICAMENTOS

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    • ABNT

      SANTOS, Carolina Alves dos et al. Influence of Pluronic'registred mark' F68 on ceftazidime biological activity in parenteral solutions. Journal of Pharmaceutical Sciences, v. 100, n. 2, p. 715-720, 2011Tradução . . Disponível em: http://dx.doi.org/10.1002/jps.22287. Acesso em: 08 ago. 2022.
    • APA

      Santos, C. A. dos, Ribeiro, G. B., Knirsch, M. C., Pessoa Junior, A., & Vessoni Penna, T. C. (2011). Influence of Pluronic'registred mark' F68 on ceftazidime biological activity in parenteral solutions. Journal of Pharmaceutical Sciences, 100( 2), 715-720. doi:10.1002/jps.22287
    • NLM

      Santos CA dos, Ribeiro GB, Knirsch MC, Pessoa Junior A, Vessoni Penna TC. Influence of Pluronic'registred mark' F68 on ceftazidime biological activity in parenteral solutions [Internet]. Journal of Pharmaceutical Sciences. 2011 ; 100( 2): 715-720.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.22287
    • Vancouver

      Santos CA dos, Ribeiro GB, Knirsch MC, Pessoa Junior A, Vessoni Penna TC. Influence of Pluronic'registred mark' F68 on ceftazidime biological activity in parenteral solutions [Internet]. Journal of Pharmaceutical Sciences. 2011 ; 100( 2): 715-720.[citado 2022 ago. 08 ] Available from: http://dx.doi.org/10.1002/jps.22287
  • Source: Journal of Pharmaceutical Sciences. Unidades: FFCLRP, FCFRP

    Subjects: NANOPARTÍCULAS, FÁRMACOS, DIFRAÇÃO POR RAIOS X

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      ROSSETTI, Fábia Cristina et al. Analysis of liquid crystalline nanoparticles by small angle X-ray diffraction: evaluation of drug and pharmaceutical additives influence on the internal structure. Journal of Pharmaceutical Sciences, v. 100, n. 7, p. 2849-2857, 2011Tradução . . Acesso em: 08 ago. 2022.
    • APA

      Rossetti, F. C., Fantini, M. C. de A., Carollo, A. R. H., Tedesco, A. C., & Bentley, M. V. L. B. (2011). Analysis of liquid crystalline nanoparticles by small angle X-ray diffraction: evaluation of drug and pharmaceutical additives influence on the internal structure. Journal of Pharmaceutical Sciences, 100( 7), 2849-2857.
    • NLM

      Rossetti FC, Fantini MC de A, Carollo ARH, Tedesco AC, Bentley MVLB. Analysis of liquid crystalline nanoparticles by small angle X-ray diffraction: evaluation of drug and pharmaceutical additives influence on the internal structure. Journal of Pharmaceutical Sciences. 2011 ; 100( 7): 2849-2857.[citado 2022 ago. 08 ]
    • Vancouver

      Rossetti FC, Fantini MC de A, Carollo ARH, Tedesco AC, Bentley MVLB. Analysis of liquid crystalline nanoparticles by small angle X-ray diffraction: evaluation of drug and pharmaceutical additives influence on the internal structure. Journal of Pharmaceutical Sciences. 2011 ; 100( 7): 2849-2857.[citado 2022 ago. 08 ]

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