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Poly-lactide-co-glycolide microparticle sizes: a rational factorial design and surface response analysis.
Namur, Jocimara Ambrósio de Moraes; Cabral-Albuquerque, Elaine Christine de Magalhães; Quintilio, Wagner; Santana, Maria Helena Andrade; Politi, Mario José; de Araujo, Pedro Soares; Lopes, Antônio Carlos; da Costa, Maria Helena Bueno.
Afiliación
  • Namur JA; Lab. De Microesferas e Lipossomas - C. de Biotecnologia-I Butantan, Av. Vital Brasil, 1500, 05503-900 Butantan, São Paulo, SP, Brasil.
J Nanosci Nanotechnol ; 6(8): 2403-7, 2006 Aug.
Article en En | MEDLINE | ID: mdl-17037847
ABSTRACT
Microsphere size is a primary determinant of solute release velocity. We present here a rational way for producing PLGA microspheres with different and controlled sizes. The following process variables were studied Stirring velocity during the second emulsion step, dispersed and continuous phases volume ratio, and poly(vinyl alcohol) concentration in the continuous phase. A full factorial experimental design 2(3) with triplicate at the central point was used to determine the influence of variables on PLGA microsphere mean size. The stirring velocity and poly(vinyl alcohol) concentration were the main variables at 0.95 significance level. An influence of PVA and stirring velocity on microspheres size is observed, there is no correlation for DP/CP volume ratio on size of microspheres. By combining the two variables--the stirring velocity and poly(vinyl alcohol) concentration, the surface response was analyzed. The increase of poly(vinyl alcohol) concentration with concomitant increase on stirring velocity produced microspheres with the lower sized. In contrast the lower poly(vinyl alcohol) concentration and the lower stirring velocity used produced the higher microspheres sized. Uniformly spherical and smooth microspheres (4-15 microm of diameter) were obtained. No significant difference was observed on Ponca S loading within the experimental region. Our results open the possibility of formulating PLGA microspheres with custom sizes performing a minimum of experiments as required for specific applications.
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Bases de datos: MEDLINE Asunto principal: Poliglactina 910 / Propiedades de Superficie / Portadores de Fármacos / Sistemas de Liberación de Medicamentos / Nanotecnología / Nanoestructuras / Nanopartículas Idioma: En Revista: J Nanosci Nanotechnol Año: 2006 Tipo del documento: Article País de afiliación: Brasil
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Bases de datos: MEDLINE Asunto principal: Poliglactina 910 / Propiedades de Superficie / Portadores de Fármacos / Sistemas de Liberación de Medicamentos / Nanotecnología / Nanoestructuras / Nanopartículas Idioma: En Revista: J Nanosci Nanotechnol Año: 2006 Tipo del documento: Article País de afiliación: Brasil