Vargas, RonnyRomero, MiquelBerasategui, TomásNarváez Narváez, David A.Ramirez, PatriciaNardi Ricart, AnnaGarcía Montoya, EncarnaPérez Lozano, PilarSuñé i Negre, Josep M. (Josep Maria)Moreno Castro, CristinaHernández Munain, CristinaSuñe, CarlosSuñé Pou, Marc2023-07-192023-07-192023-05-012215-0382https://hdl.handle.net/2445/200887Manufacturing lipid nanoparticles through microfluidic mixing can be approached from a Quality by Design perspective. Research involving critical process parameters seems to focus on the total flow and flow rate ratio, thus other process variables, such as dialysis, are underestimated. This study used a Design of Experiments to identify the influence of critical process parameters on particle size, polydispersity index, and zeta potential. A response surface Design of Experiments modeled the influence of: total flow (400 to 4000 mu L min-1); flow rate ratio (3 to 9) and dialysis (yes/no). Results suggest that dialysis is a crucial parameter that strongly influences particle size and zeta potential and moderately affects polydispersity index. The flow rate ratio's relevance decreases when dialysis is performed. As the purification method can change the influence of other process parameters, it should be an integrated part of the microfluidic manufacturing of lipid nanoparticles instead of an extra step.9 p.application/pdfengcc by-nc-nd (c) Vargas, Ronny et al., 2023http://creativecommons.org/licenses/by-nc-nd/3.0/es/Disseny d'experimentsNanopartículesTecnologia farmacèuticaExperimental designNanoparticlesPharmaceutical technologyinfo:eu-repo/semantics/article2023-06-21info:eu-repo/semantics/openAccess