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Artigo de periodico
Unravelling the role of solid lipid nanoparticles in drug delivery: journey from laboratory to clinical trial (2023)
Harish, Vancha; Mohd, Sharfuddin ; Tewari, Devesh ; Pandey, Narendra Kumar; Vishwas, Sukriti ; Babu, Malakapogu Ravindra ; Salkini, Mohamad Ayman; Rehman, Zia ur; Alotaibi, Jehan Talaq; Alotaibi, Renad Fahad; Alrashed, Fahad Abdulaziz; Prasher, Parteek; Sharma, Nitin; Gupta, Gaurav; Jakhmola, Vikash; Singh, Yogendra; Pinto, Terezinha de Jesus Andreoli ; Paudel, Keshav Raj ; Mittal, Neeraj; Singh, Thakur Gurjeet; Arora, Poonam; Dua, Kamal; Singh, Sachin Kumar
Source: Journal of Drug Delivery Science and Technology. Unidade: FCF
Subjects: NANOPARTÍCULAS, ENSAIO CLÍNICO, BIODISPONIBILIDADE, SOLUBILIDADE
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ABNT
HARISH, Vancha et al. Unravelling the role of solid lipid nanoparticles in drug delivery: journey from laboratory to clinical trial. Journal of Drug Delivery Science and Technology, v. 85, p. 1-19 art. 104616, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jddst.2023.104616. Acesso em: 05 nov. 2024.
APA
Harish, V., Mohd, S., Tewari, D., Pandey, N. K., Vishwas, S., Babu, M. R., et al. (2023). Unravelling the role of solid lipid nanoparticles in drug delivery: journey from laboratory to clinical trial. Journal of Drug Delivery Science and Technology, 85, 1-19 art. 104616. doi:10.1016/j.jddst.2023.104616
NLM
Harish V, Mohd S, Tewari D, Pandey NK, Vishwas S, Babu MR, Salkini MA, Rehman Z ur, Alotaibi JT, Alotaibi RF, Alrashed FA, Prasher P, Sharma N, Gupta G, Jakhmola V, Singh Y, Pinto T de JA, Paudel KR, Mittal N, Singh TG, Arora P, Dua K, Singh SK. Unravelling the role of solid lipid nanoparticles in drug delivery: journey from laboratory to clinical trial [Internet]. Journal of Drug Delivery Science and Technology. 2023 ; 85 1-19 art. 104616.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jddst.2023.104616
Vancouver
Harish V, Mohd S, Tewari D, Pandey NK, Vishwas S, Babu MR, Salkini MA, Rehman Z ur, Alotaibi JT, Alotaibi RF, Alrashed FA, Prasher P, Sharma N, Gupta G, Jakhmola V, Singh Y, Pinto T de JA, Paudel KR, Mittal N, Singh TG, Arora P, Dua K, Singh SK. Unravelling the role of solid lipid nanoparticles in drug delivery: journey from laboratory to clinical trial [Internet]. Journal of Drug Delivery Science and Technology. 2023 ; 85 1-19 art. 104616.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jddst.2023.104616
Artigo de periodico
PAMAM Dendrimers: a review of methodologies employed in biopharmaceutical classification (2022)
Souza, Felipe Guizze de ; Serra, Cristina Helena dos Reis ; Giarolla, Jeanine
Source: Journal of Pharmaceutical Sciences. Unidade: FCF
Subjects: SOLUBILIDADE, NANOTECNOLOGIA
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ABNT
SOUZA, Felipe Guizze de e SERRA, Cristina Helena dos Reis e GIAROLLA, Jeanine. PAMAM Dendrimers: a review of methodologies employed in biopharmaceutical classification. Journal of Pharmaceutical Sciences, v. 111, n. 10, p. 2662-2673, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.xphs.2022.07.009. Acesso em: 05 nov. 2024.
APA
Souza, F. G. de, Serra, C. H. dos R., & Giarolla, J. (2022). PAMAM Dendrimers: a review of methodologies employed in biopharmaceutical classification. Journal of Pharmaceutical Sciences, 111( 10), 2662-2673. doi:10.1016/j.xphs.2022.07.009
NLM
Souza FG de, Serra CH dos R, Giarolla J. PAMAM Dendrimers: a review of methodologies employed in biopharmaceutical classification [Internet]. Journal of Pharmaceutical Sciences. 2022 ; 111( 10): 2662-2673.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.xphs.2022.07.009
Vancouver
Souza FG de, Serra CH dos R, Giarolla J. PAMAM Dendrimers: a review of methodologies employed in biopharmaceutical classification [Internet]. Journal of Pharmaceutical Sciences. 2022 ; 111( 10): 2662-2673.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.xphs.2022.07.009
Artigo de periodico
Design of multifunctional ethosomes for topical fenretinide delivery and breast cancer chemoprevention (2021)
Apolinário, Alexsandra Conceição ; Hauschke, Leon; Nunes, Jessica Ribeiro ; Lourenço, Felipe Rebello ; Lopes, Luciana Biagini
Source: Colloids and Surfaces A. Unidades: FCF, ICB
Subjects: NEOPLASIAS MAMÁRIAS, QUIMIOTERAPIA, QUIMIOTERÁPICOS, SOLUBILIDADE, FARMACOLOGIA, CÉLULAS CULTIVADAS DE TUMOR, CITOTOXINAS
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ABNT
APOLINÁRIO, Alexsandra Conceição et al. Design of multifunctional ethosomes for topical fenretinide delivery and breast cancer chemoprevention. Colloids and Surfaces A, v. 623, n. 20, p. 1-14 art. 126745, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.colsurfa.2021.126745. Acesso em: 05 nov. 2024.
APA
Apolinário, A. C., Hauschke, L., Nunes, J. R., Lourenço, F. R., & Lopes, L. B. (2021). Design of multifunctional ethosomes for topical fenretinide delivery and breast cancer chemoprevention. Colloids and Surfaces A, 623( 20), 1-14 art. 126745. doi:10.1016/j.colsurfa.2021.126745
NLM
Apolinário AC, Hauschke L, Nunes JR, Lourenço FR, Lopes LB. Design of multifunctional ethosomes for topical fenretinide delivery and breast cancer chemoprevention [Internet]. Colloids and Surfaces A. 2021 ; 623( 20): 1-14 art. 126745.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.colsurfa.2021.126745
Vancouver
Apolinário AC, Hauschke L, Nunes JR, Lourenço FR, Lopes LB. Design of multifunctional ethosomes for topical fenretinide delivery and breast cancer chemoprevention [Internet]. Colloids and Surfaces A. 2021 ; 623( 20): 1-14 art. 126745.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.colsurfa.2021.126745
Artigo de periodico
Design space approach in the development of esculetin nanocrystals by a small-scale wet-bead milling process (2020)
Zuo, Jieyu; Araujo, Gabriel Lima Barros de ; Stephano, Marco Antônio ; Zuo, Zhengyun; Bou-Chacra, Nadia Araci ; Löbenberg, Raimar
Source: Journal of Drug Delivery Science and Technology. Unidade: FCF
Subjects: FÁRMACOS, SOLUBILIDADE
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ABNT
ZUO, Jieyu et al. Design space approach in the development of esculetin nanocrystals by a small-scale wet-bead milling process. Journal of Drug Delivery Science and Technology, v. 55, p. 1-11 art. 101486, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jddst.2019.101486. Acesso em: 05 nov. 2024.
APA
Zuo, J., Araujo, G. L. B. de, Stephano, M. A., Zuo, Z., Bou-Chacra, N. A., & Löbenberg, R. (2020). Design space approach in the development of esculetin nanocrystals by a small-scale wet-bead milling process. Journal of Drug Delivery Science and Technology, 55, 1-11 art. 101486. doi:10.1016/j.jddst.2019.101486
NLM
Zuo J, Araujo GLB de, Stephano MA, Zuo Z, Bou-Chacra NA, Löbenberg R. Design space approach in the development of esculetin nanocrystals by a small-scale wet-bead milling process [Internet]. Journal of Drug Delivery Science and Technology. 2020 ; 55 1-11 art. 101486.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jddst.2019.101486
Vancouver
Zuo J, Araujo GLB de, Stephano MA, Zuo Z, Bou-Chacra NA, Löbenberg R. Design space approach in the development of esculetin nanocrystals by a small-scale wet-bead milling process [Internet]. Journal of Drug Delivery Science and Technology. 2020 ; 55 1-11 art. 101486.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jddst.2019.101486
Artigo de periodico
Liquisolid pellets: mixture experimental design assessment of critical quality attributes influencing the manufacturing performance via extrusion-spheronization (2020)
Fonseca, Aline Benedita dos Santos; Beringhs, André O'Reilly; Ferraz, Humberto Gomes ; Stulzer, Hellen Karine; Sonaglio, Diva; Pezzini, Bianca Ramos
Source: Journal of Drug Delivery Science and Technology. Unidade: FCF
Subjects: SOLUBILIDADE, EXTRUSÃO
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ABNT
FONSECA, Aline Benedita dos Santos et al. Liquisolid pellets: mixture experimental design assessment of critical quality attributes influencing the manufacturing performance via extrusion-spheronization. Journal of Drug Delivery Science and Technology, v. 57, p. 1-9 art. 101630, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jddst.2020.101630. Acesso em: 05 nov. 2024.
APA
Fonseca, A. B. dos S., Beringhs, A. O. 'R., Ferraz, H. G., Stulzer, H. K., Sonaglio, D., & Pezzini, B. R. (2020). Liquisolid pellets: mixture experimental design assessment of critical quality attributes influencing the manufacturing performance via extrusion-spheronization. Journal of Drug Delivery Science and Technology, 57, 1-9 art. 101630. doi:10.1016/j.jddst.2020.101630
NLM
Fonseca AB dos S, Beringhs AO'R, Ferraz HG, Stulzer HK, Sonaglio D, Pezzini BR. Liquisolid pellets: mixture experimental design assessment of critical quality attributes influencing the manufacturing performance via extrusion-spheronization [Internet]. Journal of Drug Delivery Science and Technology. 2020 ; 57 1-9 art. 101630.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jddst.2020.101630
Vancouver
Fonseca AB dos S, Beringhs AO'R, Ferraz HG, Stulzer HK, Sonaglio D, Pezzini BR. Liquisolid pellets: mixture experimental design assessment of critical quality attributes influencing the manufacturing performance via extrusion-spheronization [Internet]. Journal of Drug Delivery Science and Technology. 2020 ; 57 1-9 art. 101630.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jddst.2020.101630
Artigo de periodico
Is prodrug design an approach to increase water solubility? (2019)
Sanches, Bruna Machado Araújo; Ferreira, Elizabeth Igne
Source: International Journal of Pharmaceutics. Unidade: FCF
Subjects: SOLUBILIDADE, FÁRMACOS
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ABNT
SANCHES, Bruna Machado Araújo e FERREIRA, Elizabeth Igne. Is prodrug design an approach to increase water solubility?. International Journal of Pharmaceutics, v. 568, p. 1-12 art. 118498, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.ijpharm.2019.118498. Acesso em: 05 nov. 2024.
APA
Sanches, B. M. A., & Ferreira, E. I. (2019). Is prodrug design an approach to increase water solubility? International Journal of Pharmaceutics, 568, 1-12 art. 118498. doi:10.1016/j.ijpharm.2019.118498
NLM
Sanches BMA, Ferreira EI. Is prodrug design an approach to increase water solubility? [Internet]. International Journal of Pharmaceutics. 2019 ; 568 1-12 art. 118498.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ijpharm.2019.118498
Vancouver
Sanches BMA, Ferreira EI. Is prodrug design an approach to increase water solubility? [Internet]. International Journal of Pharmaceutics. 2019 ; 568 1-12 art. 118498.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ijpharm.2019.118498
Trabalho de evento-resumo periodico
Efavirenz's solubility enhancement by amorphous solid dispersions (2019)
Nazareth Júnior, Edilson Marcelo; Serra, Cristina Helena dos Reis ; Araujo, Gabriel Lima Barros de ; Fajardo, Frank Aalonso Gavilano; Aurora-Prado, Maria Segunda ; Carvalho, Flavio Machado de Souza
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Congress of São Paulo. Unidades: FCF, IGC
Subjects: SOLUBILIDADE, HIV
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ABNT
NAZARETH JÚNIOR, Edilson Marcelo et al. Efavirenz's solubility enhancement by amorphous solid dispersions. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: http://scielousp.webhostusp.sti.usp.br/wp-content/uploads/2020/03/Anais-XXCongressodeFarmaciaSP-BJPS-final2.pdf. Acesso em: 05 nov. 2024. , 2019
APA
Nazareth Júnior, E. M., Serra, C. H. dos R., Araujo, G. L. B. de, Fajardo, F. A. G., Aurora-Prado, M. S., & Carvalho, F. M. de S. (2019). Efavirenz's solubility enhancement by amorphous solid dispersions. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Recuperado de http://scielousp.webhostusp.sti.usp.br/wp-content/uploads/2020/03/Anais-XXCongressodeFarmaciaSP-BJPS-final2.pdf
NLM
Nazareth Júnior EM, Serra CH dos R, Araujo GLB de, Fajardo FAG, Aurora-Prado MS, Carvalho FM de S. Efavirenz's solubility enhancement by amorphous solid dispersions [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2019 ; 59 res. CFSP117.[citado 2024 nov. 05 ] Available from: http://scielousp.webhostusp.sti.usp.br/wp-content/uploads/2020/03/Anais-XXCongressodeFarmaciaSP-BJPS-final2.pdf
Vancouver
Nazareth Júnior EM, Serra CH dos R, Araujo GLB de, Fajardo FAG, Aurora-Prado MS, Carvalho FM de S. Efavirenz's solubility enhancement by amorphous solid dispersions [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2019 ; 59 res. CFSP117.[citado 2024 nov. 05 ] Available from: http://scielousp.webhostusp.sti.usp.br/wp-content/uploads/2020/03/Anais-XXCongressodeFarmaciaSP-BJPS-final2.pdf
Trabalho de evento-resumo periodico
Application of analytical tool for galenical process: the usage of mixer torque rheometer to evaluate the influence of drug solubility on wet granulation parameters (2018)
Belem, Bruna Rodriguez; Kishima, Erika; Santos, Jessica Lins dos; Issa, Michele Georges ; Ferraz, Humberto Gomes
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Subjects: SOLUBILIDADE, FÁRMACOS
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ABNT
BELEM, Bruna Rodriguez et al. Application of analytical tool for galenical process: the usage of mixer torque rheometer to evaluate the influence of drug solubility on wet granulation parameters. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2018
APA
Belem, B. R., Kishima, E., Santos, J. L. dos, Issa, M. G., & Ferraz, H. G. (2018). Application of analytical tool for galenical process: the usage of mixer torque rheometer to evaluate the influence of drug solubility on wet granulation parameters. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Belem BR, Kishima E, Santos JL dos, Issa MG, Ferraz HG. Application of analytical tool for galenical process: the usage of mixer torque rheometer to evaluate the influence of drug solubility on wet granulation parameters. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 16 res. FCF028.[citado 2024 nov. 05 ]
Vancouver
Belem BR, Kishima E, Santos JL dos, Issa MG, Ferraz HG. Application of analytical tool for galenical process: the usage of mixer torque rheometer to evaluate the influence of drug solubility on wet granulation parameters. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 16 res. FCF028.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Development and characterization of efavirenz amorphous solid dispersions (2018)
Nazareth Júnior, Edilson Marcelo; Carvalho, Flavio Machado de Souza ; Araujo, Gabriel Lima Barros de ; Serra, Cristina Helena dos Reis
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidades: IGC, FCF
Subjects: ANTIRRETROVIRAIS, SOLUBILIDADE
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ABNT
NAZARETH JÚNIOR, Edilson Marcelo et al. Development and characterization of efavirenz amorphous solid dispersions. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Geociências, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/193171ea-bc55-405e-b394-a781794172b0/2920021.pdf. Acesso em: 05 nov. 2024. , 2018
APA
Nazareth Júnior, E. M., Carvalho, F. M. de S., Araujo, G. L. B. de, & Serra, C. H. dos R. (2018). Development and characterization of efavirenz amorphous solid dispersions. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Geociências, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/193171ea-bc55-405e-b394-a781794172b0/2920021.pdf
NLM
Nazareth Júnior EM, Carvalho FM de S, Araujo GLB de, Serra CH dos R. Development and characterization of efavirenz amorphous solid dispersions [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 20 res. FCF036.[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/193171ea-bc55-405e-b394-a781794172b0/2920021.pdf
Vancouver
Nazareth Júnior EM, Carvalho FM de S, Araujo GLB de, Serra CH dos R. Development and characterization of efavirenz amorphous solid dispersions [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 20 res. FCF036.[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/193171ea-bc55-405e-b394-a781794172b0/2920021.pdf
Trabalho de evento-resumo periodico
Higher hydrosolubility of rosuvastatin prodrugs (2018)
Sanches, Bruna Machado Araújo; Ferreira, Elizabeth Igne
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Subjects: SOLUBILIDADE, FÁRMACOS, BIODISPONIBILIDADE
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ABNT
SANCHES, Bruna Machado Araújo e FERREIRA, Elizabeth Igne. Higher hydrosolubility of rosuvastatin prodrugs. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2018
APA
Sanches, B. M. A., & Ferreira, E. I. (2018). Higher hydrosolubility of rosuvastatin prodrugs. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Sanches BMA, Ferreira EI. Higher hydrosolubility of rosuvastatin prodrugs. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 69 res. FCF133.[citado 2024 nov. 05 ]
Vancouver
Sanches BMA, Ferreira EI. Higher hydrosolubility of rosuvastatin prodrugs. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 69 res. FCF133.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Structural changes of Valsartan raw material under controlled atmosphere (2018)
Leon, Rosmery Merma ; Bezzon, Vinícius Danilo Nonato ; Ferraz, Humberto Gomes
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Subjects: SOLUBILIDADE, FÁRMACOS, ESTABILIDADE DOS MEDICAMENTOS
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ABNT
LEON, Rosmery Merma e BEZZON, Vinícius Danilo Nonato e FERRAZ, Humberto Gomes. Structural changes of Valsartan raw material under controlled atmosphere. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2018
APA
Leon, R. M., Bezzon, V. D. N., & Ferraz, H. G. (2018). Structural changes of Valsartan raw material under controlled atmosphere. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Leon RM, Bezzon VDN, Ferraz HG. Structural changes of Valsartan raw material under controlled atmosphere. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 57 res. 110.[citado 2024 nov. 05 ]
Vancouver
Leon RM, Bezzon VDN, Ferraz HG. Structural changes of Valsartan raw material under controlled atmosphere. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 57 res. 110.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Investigation of micronization process on physicochemical characteristics of acetazolamide: definition of design space by statistical planning approach (2018)
Kishima, Erika; Melo, Katherine Jasmine Curo; Bezzon, Vinícius Danilo Nonato ; Issa, Michele Georges ; Ferraz, Humberto Gomes
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Subjects: SOLUBILIDADE, BIODISPONIBILIDADE, FÁRMACOS
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ABNT
KISHIMA, Erika et al. Investigation of micronization process on physicochemical characteristics of acetazolamide: definition of design space by statistical planning approach. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2018
APA
Kishima, E., Melo, K. J. C., Bezzon, V. D. N., Issa, M. G., & Ferraz, H. G. (2018). Investigation of micronization process on physicochemical characteristics of acetazolamide: definition of design space by statistical planning approach. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Kishima E, Melo KJC, Bezzon VDN, Issa MG, Ferraz HG. Investigation of micronization process on physicochemical characteristics of acetazolamide: definition of design space by statistical planning approach. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 55 res. FCF106.[citado 2024 nov. 05 ]
Vancouver
Kishima E, Melo KJC, Bezzon VDN, Issa MG, Ferraz HG. Investigation of micronization process on physicochemical characteristics of acetazolamide: definition of design space by statistical planning approach. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 55 res. FCF106.[citado 2024 nov. 05 ]
Artigo de periodico
Choline-amino acid ionic liquids as green functional excipients to enhance drug solubility (2018)
Caparica, Rita; Júlio, Ana; Baby, André Rolim ; Araújo, Maria Eduarda Machado; Fernandes, Ana Sofia; Costa, João Guilherme; Almeida, Tania Santos de
Source: Pharmaceutics. Unidade: FCF
Subjects: LÍQUIDOS IÔNICOS, SOLUBILIDADE
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ABNT
CAPARICA, Rita et al. Choline-amino acid ionic liquids as green functional excipients to enhance drug solubility. Pharmaceutics, v. 10, n. 4, p. 2-13 art. 288, 2018Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics10040288. Acesso em: 05 nov. 2024.
APA
Caparica, R., Júlio, A., Baby, A. R., Araújo, M. E. M., Fernandes, A. S., Costa, J. G., & Almeida, T. S. de. (2018). Choline-amino acid ionic liquids as green functional excipients to enhance drug solubility. Pharmaceutics, 10( 4), 2-13 art. 288. doi:10.3390/pharmaceutics10040288
NLM
Caparica R, Júlio A, Baby AR, Araújo MEM, Fernandes AS, Costa JG, Almeida TS de. Choline-amino acid ionic liquids as green functional excipients to enhance drug solubility [Internet]. Pharmaceutics. 2018 ; 10( 4): 2-13 art. 288.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3390/pharmaceutics10040288
Vancouver
Caparica R, Júlio A, Baby AR, Araújo MEM, Fernandes AS, Costa JG, Almeida TS de. Choline-amino acid ionic liquids as green functional excipients to enhance drug solubility [Internet]. Pharmaceutics. 2018 ; 10( 4): 2-13 art. 288.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3390/pharmaceutics10040288
Trabalho de evento-resumo periodico
Development and characterization of solid dispersions of niclosamide (2018)
Gubitoso, Mariana Ribeiro; Bou-Chacra, Nadia Araci ; Carvalho, Flavio Machado de Souza ; Araujo, Gabriel Lima Barros de
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidades: IGC, FCF
Subjects: SOLUBILIDADE, ANTIPARASITÁRIOS
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ABNT
GUBITOSO, Mariana Ribeiro et al. Development and characterization of solid dispersions of niclosamide. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Geociências, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/2f3c95a1-ebe7-443f-b916-b482dbdf72a3/2919331.pdf. Acesso em: 05 nov. 2024. , 2018
APA
Gubitoso, M. R., Bou-Chacra, N. A., Carvalho, F. M. de S., & Araujo, G. L. B. de. (2018). Development and characterization of solid dispersions of niclosamide. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Geociências, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/2f3c95a1-ebe7-443f-b916-b482dbdf72a3/2919331.pdf
NLM
Gubitoso MR, Bou-Chacra NA, Carvalho FM de S, Araujo GLB de. Development and characterization of solid dispersions of niclosamide [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 14 res. FCF024.[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/2f3c95a1-ebe7-443f-b916-b482dbdf72a3/2919331.pdf
Vancouver
Gubitoso MR, Bou-Chacra NA, Carvalho FM de S, Araujo GLB de. Development and characterization of solid dispersions of niclosamide [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 14 res. FCF024.[citado 2024 nov. 05 ] Available from: https://repositorio.usp.br/directbitstream/2f3c95a1-ebe7-443f-b916-b482dbdf72a3/2919331.pdf
Artigo de periodico
In silico simulation of dissolution profiles for development of extended-release doxazosin tablets (2018)
Duque, Marcelo Dutra ; Issa, Michele Georges ; Silva, Daniela Amaral ; Barbosa, Eduardo José ; Löbenberg, Raimar ; Ferraz, Humberto Gomes
Source: Dissolution Technologies. Unidade: FCF
Subjects: SOLUBILIDADE, FÁRMACOS, HIPERTENSÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DUQUE, Marcelo Dutra et al. In silico simulation of dissolution profiles for development of extended-release doxazosin tablets. Dissolution Technologies, v. 25, n. 4, p. 14-21, 2018Tradução . . Disponível em: https://doi.org/10.14227/DT250418P14. Acesso em: 05 nov. 2024.
APA
Duque, M. D., Issa, M. G., Silva, D. A., Barbosa, E. J., Löbenberg, R., & Ferraz, H. G. (2018). In silico simulation of dissolution profiles for development of extended-release doxazosin tablets. Dissolution Technologies, 25( 4), 14-21. doi:10.14227/DT250418P14
NLM
Duque MD, Issa MG, Silva DA, Barbosa EJ, Löbenberg R, Ferraz HG. In silico simulation of dissolution profiles for development of extended-release doxazosin tablets [Internet]. Dissolution Technologies. 2018 ; 25( 4): 14-21.[citado 2024 nov. 05 ] Available from: https://doi.org/10.14227/DT250418P14
Vancouver
Duque MD, Issa MG, Silva DA, Barbosa EJ, Löbenberg R, Ferraz HG. In silico simulation of dissolution profiles for development of extended-release doxazosin tablets [Internet]. Dissolution Technologies. 2018 ; 25( 4): 14-21.[citado 2024 nov. 05 ] Available from: https://doi.org/10.14227/DT250418P14
Artigo de periodico
Solubility evaluation of didanosine: a comparison between the equilibrium method and intrinsic dissolution for biopharmaceutics classification purposes (2017)
Dezani, André Bersani; Dezani, Thaisa Marinho; Ferreira, Julie Caroline Ferrari; Serra, Cristina Helena dos Reis
Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: FCF
Subjects: SOLUBILIDADE, MEDICAMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEZANI, André Bersani et al. Solubility evaluation of didanosine: a comparison between the equilibrium method and intrinsic dissolution for biopharmaceutics classification purposes. Brazilian Journal of Pharmaceutical Sciences, v. 53, n. 2, p. 1-8 art. e16128, 2017Tradução . . Disponível em: https://doi.org/10.1590/s2175-97902017000216128. Acesso em: 05 nov. 2024.
APA
Dezani, A. B., Dezani, T. M., Ferreira, J. C. F., & Serra, C. H. dos R. (2017). Solubility evaluation of didanosine: a comparison between the equilibrium method and intrinsic dissolution for biopharmaceutics classification purposes. Brazilian Journal of Pharmaceutical Sciences, 53( 2), 1-8 art. e16128. doi:10.1590/s2175-97902017000216128
NLM
Dezani AB, Dezani TM, Ferreira JCF, Serra CH dos R. Solubility evaluation of didanosine: a comparison between the equilibrium method and intrinsic dissolution for biopharmaceutics classification purposes [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53( 2): 1-8 art. e16128.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s2175-97902017000216128
Vancouver
Dezani AB, Dezani TM, Ferreira JCF, Serra CH dos R. Solubility evaluation of didanosine: a comparison between the equilibrium method and intrinsic dissolution for biopharmaceutics classification purposes [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53( 2): 1-8 art. e16128.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s2175-97902017000216128
Trabalho de evento-resumo
Nanoemulsão catiônica contendo rifampicina: preparação e caracterização físico-química (2017)
Iwamoto, Giovana Mika Tanabe; Henostroza, Mirla Anali Bazan; Bou-Chacra, Nadia Araci
Source: Resumos. Conference titles: Simpósio Internacional de Iniciação Científica e Tecnológica da USP/SIICUSP. Unidade: FCF
Subjects: ANTIBIÓTICOS, SOLUBILIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IWAMOTO, Giovana Mika Tanabe e HENOSTROZA, Mirla Anali Bazan e BOU-CHACRA, Nadia Araci. Nanoemulsão catiônica contendo rifampicina: preparação e caracterização físico-química. 2017, Anais.. São Paulo: Pró-Reitoria de Pesquisa/USP, 2017. Disponível em: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210. Acesso em: 05 nov. 2024.
APA
Iwamoto, G. M. T., Henostroza, M. A. B., & Bou-Chacra, N. A. (2017). Nanoemulsão catiônica contendo rifampicina: preparação e caracterização físico-química. In Resumos. São Paulo: Pró-Reitoria de Pesquisa/USP. Recuperado de https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
NLM
Iwamoto GMT, Henostroza MAB, Bou-Chacra NA. Nanoemulsão catiônica contendo rifampicina: preparação e caracterização físico-química [Internet]. Resumos. 2017 ;[citado 2024 nov. 05 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Vancouver
Iwamoto GMT, Henostroza MAB, Bou-Chacra NA. Nanoemulsão catiônica contendo rifampicina: preparação e caracterização físico-química [Internet]. Resumos. 2017 ;[citado 2024 nov. 05 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Artigo de periodico
Evolution of choice of solubility and dissolution media after two decades of biopharmaceutical classification system (2017)
Bou-Chacra, Nadia Araci ; Melo, Katherine Jasmine Curo; Morales, Ivan Andrés Cordova; Stippler, Erika S; Kesisoglou, Filippos; Yazdanian, Mehran; Löbenberg, Raimar
Source: AAPS Journal. Unidade: FCF
Subjects: SOLUBILIDADE, BIOFARMÁCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BOU-CHACRA, Nadia Araci et al. Evolution of choice of solubility and dissolution media after two decades of biopharmaceutical classification system. AAPS Journal, v. 19, n. 4, p. 989-1001, 2017Tradução . . Disponível em: https://doi.org/10.1208/s12248-017-0085-5. Acesso em: 05 nov. 2024.
APA
Bou-Chacra, N. A., Melo, K. J. C., Morales, I. A. C., Stippler, E. S., Kesisoglou, F., Yazdanian, M., & Löbenberg, R. (2017). Evolution of choice of solubility and dissolution media after two decades of biopharmaceutical classification system. AAPS Journal, 19( 4), 989-1001. doi:10.1208/s12248-017-0085-5
NLM
Bou-Chacra NA, Melo KJC, Morales IAC, Stippler ES, Kesisoglou F, Yazdanian M, Löbenberg R. Evolution of choice of solubility and dissolution media after two decades of biopharmaceutical classification system [Internet]. AAPS Journal. 2017 ; 19( 4): 989-1001.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1208/s12248-017-0085-5
Vancouver
Bou-Chacra NA, Melo KJC, Morales IAC, Stippler ES, Kesisoglou F, Yazdanian M, Löbenberg R. Evolution of choice of solubility and dissolution media after two decades of biopharmaceutical classification system [Internet]. AAPS Journal. 2017 ; 19( 4): 989-1001.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1208/s12248-017-0085-5
Artigo de periodico
In silico and in vitro prediction of gastrointestinalabsorpti on from potential drug eremantholide C (2017)
Caldeira, Tamires G; Guimarães, Dênia A. Saúde; Dezani, André Bersani; Serra, Cristina Helena dos Reis ; Souza, Jacqueline de
Source: Journal of Pharmacy and Pharmacology. Unidade: FCF
Subjects: SOLUBILIDADE, ABSORÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CALDEIRA, Tamires G et al. In silico and in vitro prediction of gastrointestinalabsorpti on from potential drug eremantholide C. Journal of Pharmacy and Pharmacology, v. 69, n. 11, p. 1468-1476, 2017Tradução . . Disponível em: https://www-ncbi-nlm-nih-gov.ez67.periodicos.capes.gov.br/pubmed/28722112. Acesso em: 05 nov. 2024.
APA
Caldeira, T. G., Guimarães, D. A. S., Dezani, A. B., Serra, C. H. dos R., & Souza, J. de. (2017). In silico and in vitro prediction of gastrointestinalabsorpti on from potential drug eremantholide C. Journal of Pharmacy and Pharmacology, 69( 11), 1468-1476. Recuperado de https://www-ncbi-nlm-nih-gov.ez67.periodicos.capes.gov.br/pubmed/28722112
NLM
Caldeira TG, Guimarães DAS, Dezani AB, Serra CH dos R, Souza J de. In silico and in vitro prediction of gastrointestinalabsorpti on from potential drug eremantholide C [Internet]. Journal of Pharmacy and Pharmacology. 2017 ; 69( 11): 1468-1476.[citado 2024 nov. 05 ] Available from: https://www-ncbi-nlm-nih-gov.ez67.periodicos.capes.gov.br/pubmed/28722112
Vancouver
Caldeira TG, Guimarães DAS, Dezani AB, Serra CH dos R, Souza J de. In silico and in vitro prediction of gastrointestinalabsorpti on from potential drug eremantholide C [Internet]. Journal of Pharmacy and Pharmacology. 2017 ; 69( 11): 1468-1476.[citado 2024 nov. 05 ] Available from: https://www-ncbi-nlm-nih-gov.ez67.periodicos.capes.gov.br/pubmed/28722112
Artigo de periodico
Intrinsic dissolution simulation of highly and poorly soluble drugs for BCS solubility classification (2017)
Duque, Marcelo Dutra; Issa, Michele Georges ; Silva, Daniela Amaral; Kakuda, Beatriz Ayumi Sakamoto; Rodrigues, Leticia Norma Carpentieri; Löbenberg, Raimar; Ferraz, Humberto Gomes
Source: Dissolution Technologies. Unidade: FCF
Subjects: SOLUBILIDADE, FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DUQUE, Marcelo Dutra et al. Intrinsic dissolution simulation of highly and poorly soluble drugs for BCS solubility classification. Dissolution Technologies, v. 24, n. 4, p. 6-11, 2017Tradução . . Disponível em: https://doi.org/10.14227/DT240417P6. Acesso em: 05 nov. 2024.
APA
Duque, M. D., Issa, M. G., Silva, D. A., Kakuda, B. A. S., Rodrigues, L. N. C., Löbenberg, R., & Ferraz, H. G. (2017). Intrinsic dissolution simulation of highly and poorly soluble drugs for BCS solubility classification. Dissolution Technologies, 24( 4), 6-11. doi:10.14227/DT240417P6
NLM
Duque MD, Issa MG, Silva DA, Kakuda BAS, Rodrigues LNC, Löbenberg R, Ferraz HG. Intrinsic dissolution simulation of highly and poorly soluble drugs for BCS solubility classification [Internet]. Dissolution Technologies. 2017 ; 24( 4): 6-11.[citado 2024 nov. 05 ] Available from: https://doi.org/10.14227/DT240417P6
Vancouver
Duque MD, Issa MG, Silva DA, Kakuda BAS, Rodrigues LNC, Löbenberg R, Ferraz HG. Intrinsic dissolution simulation of highly and poorly soluble drugs for BCS solubility classification [Internet]. Dissolution Technologies. 2017 ; 24( 4): 6-11.[citado 2024 nov. 05 ] Available from: https://doi.org/10.14227/DT240417P6

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