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Free-Standing Hierarchically Porous Silica Nanoparticle Superstructures: Bridging the Nano- to Microscale for Tailorable Delivery of Small and Large Therapeutics.
Palvai, Sandeep; Kpeglo, Delanyo; Newham, George; Peyman, Sally A; Evans, Stephen D; Ong, Zhan Yuin.
Afiliación
  • Palvai S; School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, U.K.
  • Kpeglo D; School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, U.K.
  • Newham G; School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, U.K.
  • Peyman SA; School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, U.K.
  • Evans SD; Leeds Institute of Medical Research at St James, School of Medicine, University of Leeds, Leeds LS2 9JT, U.K.
  • Ong ZY; School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, U.K.
ACS Appl Mater Interfaces ; 16(5): 5568-5581, 2024 Feb 07.
Article en En | MEDLINE | ID: mdl-38270578
ABSTRACT
Nanoscale colloidal self-assembly is an exciting approach to yield superstructures with properties distinct from those of individual nanoparticles. However, the bottom-up self-assembly of 3D nanoparticle superstructures typically requires extensive chemical functionalization, harsh conditions, and a long preparation time, which are undesirable for biomedical applications. Here, we report the directional freezing of porous silica nanoparticles (PSiNPs) as a simple and versatile technique to create anisotropic 3D superstructures with hierarchical porosity afforded by microporous PSiNPs and newly generated meso- and macropores between the PSiNPs. By varying the PSiNP building block size, the interparticle pore sizes can be readily tuned. The newly created hierarchical pores greatly augment the loading of a small molecule-anticancer drug, doxorubicin (Dox), and a large macromolecule, lysozyme (Lyz). Importantly, Dox loading into both the micro- and meso/macropores of the nanoparticle assemblies not only gave a pore size-dependent drug release but also significantly extended the drug release to 25 days compared to a much shorter 7 or 11 day drug release from Dox loaded into either the micro- or meso/macropores only. Moreover, a unique temporal drug release profile, with a higher and faster release of Lyz from the larger interparticle macropores than Dox from the smaller PSiNP micropores, was observed. Finally, the formulation of the Dox-loaded superstructures within a composite hydrogel induces prolonged growth inhibition in a 3D spheroid model of pancreatic ductal adenocarcinoma. This study presents a facile modular approach for the rapid assembly of drug-loaded superstructures in fully aqueous environments and demonstrates their potential as highly tailorable and sustained delivery systems for diverse therapeutics.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nanopartículas / Antineoplásicos Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nanopartículas / Antineoplásicos Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos