Tavares Luiz, MarcelaSantos Rosa Viegas, JulianaPalma Abriata, JulianaViegas, FelipeTesta Moura de Carvalho Vicentini, FabianaLopes Badra Bentley, Maria VitóriaChorilli, Marlus [UNESP]Maldonado Marchetti, JulianaTapia-Blácido, Delia Rita2022-05-012022-05-012021-08-01European Journal of Pharmaceutics and Biopharmaceutics, v. 165, p. 127-148.1873-34410939-6411http://hdl.handle.net/11449/233175Nanotechnology 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.127-148engBox-Behnken DesignCentral Composite DesignFractional Factorial DesignFull Factorial DesignNanomedicineNanotechnologyPlackett-Burman DesignQuality by DesignResponse Surface MethodologyDesign of experiments (DoE) to develop and to optimize nanoparticles as drug delivery systemsArtigo10.1016/j.ejpb.2021.05.0112-s2.0-85108303638