dc.creatorSantos, Karen C.
dc.creatorSilva, Maria Fatima G. F.
dc.creatorPereira Filho, Edenir R.
dc.creatorFernandes, Joao B.
dc.creatorPolikarpov, Igor
dc.creatorForim, Moacir R.
dc.date.accessioned2016-03-08T18:31:21Z
dc.date.accessioned2018-07-04T16:54:11Z
dc.date.available2016-03-08T18:31:21Z
dc.date.available2018-07-04T16:54:11Z
dc.date.created2016-03-08T18:31:21Z
dc.date.issued2012-07
dc.identifierNanotechnology, Science and Applications,Macclesfield : Dove Medical,v. 5, p. 37-48, July 2012
dc.identifier1177-8903
dc.identifierhttp://www.producao.usp.br/handle/BDPI/49927
dc.identifier10.2147/NSA.S32837
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1641937
dc.description.abstractThis present investigation deals with the development and optimization of polymeric nanoparticle systems loaded with 3,5,3′-triiodothyroacetic acid (Triac). A '2 POT. 11-6' fractional factorial design and another '2 POT. 2' factorial design were used to study the contrasts on particle size distribution, morphology, surface charge, drug content, entrapment efficiency, and in vitro drug release profiles. The independent variables were the concentration of Triac, type and quantity of both polymer and oil, quantity of Span™ 60 and Tween® 80, volume of solvent and water, and velocity of both magnetic stirring and the transfer of the organic phase into the aqueous solution. The results of optimized formulations showed a narrow size distribution with a polydispersity index lower than 0.200. The particle sizes were on average 159.6 nm and 285.6 nm for nanospheres and nanocapsules, respectively. The zeta potential was higher than 20 mV (in module) and the entrapment efficiency was nearly 100%. A high-performance liquid chromatography method was developed, validated, and efficiently applied to Triac quantification in colloidal suspension. The main independent variables were the type and quantity of the polymer and oil. In vitro drug release profile depicted several features to sustain Triac release. Different formulations showed various release rates indicating an interaction between Triac and other formulation compounds such as polymer and/or oil quantity. Two different models were identified (biexponential and monoexponential) that allowed the control of both the release rate and Triac concentration. Thus, the prepared nanoparticles described here may be of clinical importance in delivering Triac for thyroid treatment.
dc.languageeng
dc.publisherDove Medical
dc.publisherMacclesfield
dc.relationNanotechnology, Science and Applications
dc.rightsCopyright by the authors
dc.rightsopenAccess
dc.subjectTriac
dc.subjectNanoparticles
dc.subjectOptimization
dc.subjectFactorial design of experiments
dc.subjectHPLC analytical method
dc.titlePolymeric nanoparticles loaded with the 3,5,3'-triiodothyroacetic acid (Triac), a thyroid hormone: factorial design, characterization, and release kinetics
dc.typeArtículos de revistas


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