Design of experiments (DoE) to develop and to optimize nanoparticles as drug delivery systems

dc.contributor.authorTavares Luiz, Marcela
dc.contributor.authorSantos Rosa Viegas, Juliana
dc.contributor.authorPalma Abriata, Juliana
dc.contributor.authorViegas, Felipe
dc.contributor.authorTesta Moura de Carvalho Vicentini, Fabiana
dc.contributor.authorLopes Badra Bentley, Maria Vitória
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorMaldonado Marchetti, Juliana
dc.contributor.authorTapia-Blácido, Delia Rita
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-05-01T05:29:28Z
dc.date.available2022-05-01T05:29:28Z
dc.date.issued2021-08-01
dc.description.abstractNanotechnology has been widely applied to develop drug delivery systems to improve therapeutic performance. The effectiveness of these systems is intrinsically related to their physicochemical properties, so their biological responses are highly susceptible to factors such as the type and quantity of each material that is employed in their synthesis and to the method that is used to produce them. In this context, quality-oriented manufacturing of nanoparticles has been an important strategy to understand and to optimize the factors involved in their production. For this purpose, Design of Experiment (DoE) tools have been applied to obtain enough knowledge about the process and hence achieve high-quality products. This review aims to set up the bases to implement DoE as a strategy to improve the manufacture of nanocarriers and to discuss the main factors involved in the production of the most common nanocarriers employed in the pharmaceutical field.en
dc.description.affiliationSchool of Pharmaceutical Sciences of Ribeirao Preto University of Sao Paulo
dc.description.affiliationDepartment of Computer Science Federal University of Minas Gerais, Belo Horizonte
dc.description.affiliationSchool of Pharmaceutical Sciences Sao Paulo State University
dc.description.affiliationDepartment of Chemistry Faculty of Philosophy Sciences and Letters of Ribeirao Preto University of São Paulo
dc.description.affiliationUnespSchool of Pharmaceutical Sciences Sao Paulo State University
dc.format.extent127-148
dc.identifierhttp://dx.doi.org/10.1016/j.ejpb.2021.05.011
dc.identifier.citationEuropean Journal of Pharmaceutics and Biopharmaceutics, v. 165, p. 127-148.
dc.identifier.doi10.1016/j.ejpb.2021.05.011
dc.identifier.issn1873-3441
dc.identifier.issn0939-6411
dc.identifier.scopus2-s2.0-85108303638
dc.identifier.urihttp://hdl.handle.net/11449/233175
dc.language.isoeng
dc.relation.ispartofEuropean Journal of Pharmaceutics and Biopharmaceutics
dc.sourceScopus
dc.subjectBox-Behnken Design
dc.subjectCentral Composite Design
dc.subjectFractional Factorial Design
dc.subjectFull Factorial Design
dc.subjectNanomedicine
dc.subjectNanotechnology
dc.subjectPlackett-Burman Design
dc.subjectQuality by Design
dc.subjectResponse Surface Methodology
dc.titleDesign of experiments (DoE) to develop and to optimize nanoparticles as drug delivery systemsen
dc.typeArtigo
unesp.departmentFármacos e Medicamentos - FCFpt

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