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Nanoporous hybrid core-shell nanoparticles for sequential release.
Jahns, Mandy; Warwas, Dawid Peter; Krey, Marc Robert; Nolte, Katharina; König, Sandra; Fröba, Michael; Behrens, Peter.
Afiliação
  • Jahns M; Institute for Inorganic Chemistry, Gottfried Wilhelm Leibniz University Hannover, 30167 Hannover, Germany. peter.behrens@acb.uni-hannover.de and Cluster of Excellence Hearing4all, Hannover, Germany.
  • Warwas DP; Institute for Inorganic Chemistry, Gottfried Wilhelm Leibniz University Hannover, 30167 Hannover, Germany. peter.behrens@acb.uni-hannover.de.
  • Krey MR; Institute for Inorganic Chemistry, Gottfried Wilhelm Leibniz University Hannover, 30167 Hannover, Germany. peter.behrens@acb.uni-hannover.de.
  • Nolte K; Institute for Inorganic Chemistry, Gottfried Wilhelm Leibniz University Hannover, 30167 Hannover, Germany. peter.behrens@acb.uni-hannover.de.
  • König S; Institute of Inorganic and Applied Chemistry, University of Hamburg, 20146 Hamburg, Germany.
  • Fröba M; Institute of Inorganic and Applied Chemistry, University of Hamburg, 20146 Hamburg, Germany.
  • Behrens P; Institute for Inorganic Chemistry, Gottfried Wilhelm Leibniz University Hannover, 30167 Hannover, Germany. peter.behrens@acb.uni-hannover.de and Cluster of Excellence Hearing4all, Hannover, Germany.
J Mater Chem B ; 8(4): 776-786, 2020 01 28.
Article em En | MEDLINE | ID: mdl-31898715
In this article, a new type of core-shell nanoparticle is introduced. In contrast to most reported core-shell systems, the particles presented here consist of a porous core as well as a porous shell using only non-metal materials. The core-shell nanoparticles were successfully synthesized using nanoporous silica nanoparticles (NPSNPs) as the starting material, which were coated with nanoporous phenylene-bridged organosilica, resulting in a total particle diameter of about 80 nm. The combination of a hydrophilic nanoporous silica core and a more hydrophobic nanoporous organosilica shell provides regions of different chemical character and slightly different pore sizes within one particle. These different properties combined in one particle enable the selective adsorption of guest molecules at different parts of the particle depending on the molecular charge and polarity. On the other hand, the core-shell make-up of the particles provides a sequential release of guest molecules adsorbed at different parts of the nanoparticles. As a proof of concept, loading and release experiments with dyes were performed using non polar fluorescein and polar and charged methylene blue as model guest molecules. Non polar fluorescein is mostly adsorbed on the hydrophobic organosilica shell and therefore quickly released whereas the polar methylene blue, accumulated in the hydrophilic silica core, is only released subsequently. This occurs in small doses for an extended time corresponding to a sustained release over at least one year, controlled by the organosilica shell which acts as a diffusion barrier. An initial experiment with two drugs - non polar ibuprofen and polar and charged procaine hydrochloride - has been carried out as well and shows that the core-shell nanoparticles presented here can also be used for the sequential release of more relevant combinations of molecules.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Procaína / Ibuprofeno / Compostos de Organossilício / Dióxido de Silício / Nanopartículas Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Procaína / Ibuprofeno / Compostos de Organossilício / Dióxido de Silício / Nanopartículas Idioma: En Ano de publicação: 2020 Tipo de documento: Article