Quantitative Analysis of Porous Silicon Nanoparticles Functionalization by 1H NMR

dc.contributor.authorCheng Ruoyu
dc.contributor.authorShiqi Wang
dc.contributor.authorMoslova Karina
dc.contributor.authorMäkilä Ermei
dc.contributor.authorSalonen Jarno
dc.contributor.authorLi Jiachen
dc.contributor.authorHirvonen Jouni
dc.contributor.authorXia Bing
dc.contributor.authorSantos Hélder A.
dc.contributor.organizationfi=teollisuusfysiikan laboratorio|en=Laboratory of Industrial Physics|
dc.contributor.organization-code1.2.246.10.2458963.20.66904373678
dc.converis.publication-id66881764
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/66881764
dc.date.accessioned2022-10-27T11:53:35Z
dc.date.available2022-10-27T11:53:35Z
dc.description.abstract<p>Porous silicon (PSi) nanoparticles have been applied in various fields, such as catalysis, imaging, and biomedical applications, because of their large specific surface area, easily modifiable surface chemistry, biocompatibility, and biodegradability. For biomedical applications, it is important to precisely control the surface modification of PSi-based materials and quantify the functionalization density, which determines the nanoparticle’s behavior in the biological system. Therefore, we propose here an optimized solution to quantify the functionalization groups on PSi, based on the nuclear magnetic resonance (NMR) method by combining the hydrolysis with standard 1H NMR experiments. We optimized the hydrolysis conditions to degrade the PSi, providing mobility to the molecules for NMR detection. The NMR parameters were also optimized by relaxation delay and the number of scans to provide reliable NMR spectra. With an internal standard, we quantitatively analyzed the surficial amine groups and their sequential modification of polyethylene glycol. Our investigation provides a reliable, fast, and straightforward method in quantitative analysis of the surficial modification characterization of PSi requiring a small amount of sample.</p>
dc.format.pagerange4132
dc.format.pagerange4139
dc.identifier.eissn2373-9878
dc.identifier.jour-issn2373-9878
dc.identifier.olddbid172612
dc.identifier.oldhandle10024/155706
dc.identifier.urihttps://www.utupub.fi/handle/11111/54444
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acsbiomaterials.1c00440
dc.identifier.urnURN:NBN:fi-fe2021093047966
dc.language.isoen
dc.okm.affiliatedauthorMäkilä, Ermei
dc.okm.affiliatedauthorSalonen, Jarno
dc.okm.discipline114 Physical sciencesen_GB
dc.okm.discipline114 Fysiikkafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAmerican Chemical Society
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1021/acsbiomaterials.1c00440
dc.relation.ispartofjournalACS Biomaterials Science and Engineering
dc.relation.issue10
dc.relation.volume8
dc.source.identifierhttps://www.utupub.fi/handle/10024/155706
dc.titleQuantitative Analysis of Porous Silicon Nanoparticles Functionalization by 1H NMR
dc.year.issued2022

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