Biophotonic composite scaffolds for controlled nitric oxide release upon NIR excitation

dc.contributor.authorGhanavati, S.
dc.contributor.authorMagalhaes, E. Santos
dc.contributor.authorNguyen, C.
dc.contributor.authorBondzior, B.
dc.contributor.authorLastusaari, M.
dc.contributor.authorAnker, J.N.
dc.contributor.authorDraganski, A.
dc.contributor.authorPetit, L.
dc.contributor.authorMassera, J.
dc.contributor.organizationfi=kemian laitos|en=Department of Chemistry|
dc.contributor.organization-code1.2.246.10.2458963.20.27622076134
dc.converis.publication-id459051865
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/459051865
dc.date.accessioned2025-08-28T00:34:01Z
dc.date.available2025-08-28T00:34:01Z
dc.description.abstract<p>For the first time, the preparation of 3D biophotonic scaffolds is reported. Scaffolds are prepared using the porogen burn-off technique and are capable of converting NIR to green emission, used to release nitric oxide from S-Nitroso-N-Acetylpenicillamine. NIR to green conversion is obtained by mixing CaWO<sub>4</sub> crystals (codoped with Yb<sup>3+</sup> and Er<sup>3+</sup>) with bioactive borosilicate glass prior to the sintering process. The scaffold fabrication process has a detrimental impact on the upconversion properties of the crystals embedded in the porous scaffold due to the formation of internal/surface crystalline defects and surface chemical bonds in the crystals. Nonetheless, we demonstrate that the brightness of the green emission, under 980 nm pumping, is sufficient to release nitric oxide from the scaffold covered with S-Nitroso-N-Acetylpenicillamine. Addition of upconverter crystals, in the bioactive scaffold, has no impact on porosity, mechanical properties, reactivity in simulated body fluid nor cytocompatibility. The progressive dissolution of the scaffold, associated with the precipitation of a reactive layer (HA), has no noticeable influence on the green emission under 980 nm pumping, showing that the development of such biophotonic scaffolds opens the path to light actuated drug release in a spatial–temporal manner, in vivo. Degradation of the up-converter particles does not lead to differences in cells viability.<br></p>
dc.identifier.eissn1873-4197
dc.identifier.jour-issn0264-1275
dc.identifier.olddbid205954
dc.identifier.oldhandle10024/188981
dc.identifier.urihttps://www.utupub.fi/handle/11111/37582
dc.identifier.urlhttps://doi.org/10.1016/j.matdes.2024.113369
dc.identifier.urnURN:NBN:fi-fe2025082787175
dc.language.isoen
dc.okm.affiliatedauthorLastusaari, Mika
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline116 Kemiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier BV
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.articlenumber113369
dc.relation.doi10.1016/j.matdes.2024.113369
dc.relation.ispartofjournalMaterials and Design
dc.relation.volume247
dc.source.identifierhttps://www.utupub.fi/handle/10024/188981
dc.titleBiophotonic composite scaffolds for controlled nitric oxide release upon NIR excitation
dc.year.issued2024

Tiedostot

Näytetään 1 - 1 / 1
Ladataan...
Name:
1-s2.0-S0264127524007445-main.pdf
Size:
2.94 MB
Format:
Adobe Portable Document Format