Investigation of silicon nanoparticles produced by centrifuge chemical vapor deposition for applications in therapy and diagnostics.
Animals
Cell Survival
/ drug effects
Centrifugation
Drug Carriers
/ administration & dosage
Drug Compounding
/ methods
Female
Indium Radioisotopes
/ administration & dosage
Injections, Intravenous
Mice
Models, Animal
Nanoparticles
/ administration & dosage
Porosity
RAW 264.7 Cells
Radiopharmaceuticals
/ administration & dosage
Silicon
/ administration & dosage
Tissue Distribution
Toxicity Tests, Acute
Biodistribution
Nanoparticles
Porous silicon
Production
Toxicity
Journal
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
03
05
2020
revised:
23
10
2020
accepted:
27
11
2020
pubmed:
7
12
2020
medline:
21
9
2021
entrez:
6
12
2020
Statut:
ppublish
Résumé
Porous silicon (PSi) is a biocompatible and biodegradable material, which can be utilized in biomedical applications. It has several favorable properties, which makes it an excellent material for building engineered nanosystems for drug delivery and diagnostic purposes. One significant hurdle for commercial applications of PSi is the lack of industrial scale production of nanosized PSi particles. Here, we report a novel two-step production method for PSi nanoparticles. The method is based on centrifuge chemical vapor deposition (cCVD) of elemental silicon in an industrial scale reactor followed by electrochemical post-processing to porous particles. Physical properties, biocompatibility and in vivo biodistribution of the cCVD produced nanoparticles were investigated and compared to PSi nanoparticles conventionally produced from silicon wafers by pulse electrochemical etching. Our results demonstrate that the cCVD production provides PSi nanoparticles with comparable physical and biological quality to the conventional method. This method may circumvent several limitations of the conventional method such as the requirements for high purity monocrystalline silicon substrates as starting material and the material losses during the top-down milling process of the pulse-etched films to porous nanoparticles. However, the electroless etching required for the porosification of cCVD-produced nanoparticles limited control over the pore size, but is amenable for scaling of the production to industrial requirements.
Identifiants
pubmed: 33279602
pii: S0939-6411(20)30355-6
doi: 10.1016/j.ejpb.2020.11.022
pii:
doi:
Substances chimiques
Drug Carriers
0
Indium Radioisotopes
0
Radiopharmaceuticals
0
Indium-111
E9NGC49E0T
Silicon
Z4152N8IUI
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
254-265Informations de copyright
Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.