Investigation of silicon nanoparticles produced by centrifuge chemical vapor deposition for applications in therapy and diagnostics

dc.contributor.authorLumen Dave
dc.contributor.authorWang Shiqi
dc.contributor.authorMäkilä Ermei
dc.contributor.authorImlimthan Surachet
dc.contributor.authorSarparanta Mirkka
dc.contributor.authorCorreia Alexandra
dc.contributor.authorWesterveld Haug Christina
dc.contributor.authorHirvonen Jouni
dc.contributor.authorSantos Hélder A
dc.contributor.authorAiraksinen Anu J
dc.contributor.authorFiltvedt Werener
dc.contributor.authorSalonen Jarno
dc.contributor.organizationfi=kemian laitos|en=Department of Chemistry|
dc.contributor.organizationfi=teollisuusfysiikan laboratorio|en=Laboratory of Industrial Physics|
dc.contributor.organization-code1.2.246.10.2458963.20.27622076134
dc.contributor.organization-code1.2.246.10.2458963.20.66904373678
dc.converis.publication-id51409921
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/51409921
dc.date.accessioned2022-10-28T14:24:39Z
dc.date.available2022-10-28T14:24:39Z
dc.description.abstractPorous 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.
dc.format.pagerange254
dc.format.pagerange265
dc.identifier.eissn1873-3441
dc.identifier.jour-issn0939-6411
dc.identifier.olddbid188103
dc.identifier.oldhandle10024/171197
dc.identifier.urihttps://www.utupub.fi/handle/11111/39822
dc.identifier.urlhttps://doi.org/10.1016/j.ejpb.2020.11.022
dc.identifier.urnURN:NBN:fi-fe2021042826430
dc.language.isoen
dc.okm.affiliatedauthorMäkilä, Ermei
dc.okm.affiliatedauthorSalonen, Jarno
dc.okm.affiliatedauthorAiraksinen, Anu
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline215 Chemical engineeringen_GB
dc.okm.discipline221 Nanotechnologyen_GB
dc.okm.discipline317 Pharmacyen_GB
dc.okm.discipline116 Kemiafi_FI
dc.okm.discipline215 Teknillinen kemia, kemian prosessitekniikkafi_FI
dc.okm.discipline221 Nanoteknologiafi_FI
dc.okm.discipline317 Farmasiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.doi10.1016/j.ejpb.2020.11.022
dc.relation.ispartofjournalEuropean Journal of Pharmaceutics and Biopharmaceutics
dc.relation.volume158
dc.source.identifierhttps://www.utupub.fi/handle/10024/171197
dc.titleInvestigation of silicon nanoparticles produced by centrifuge chemical vapor deposition for applications in therapy and diagnostics
dc.year.issued2021

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