Semi‐solid 3D printing of mesoporous silica nanoparticle‐incorporated xeno‐free nanomaterial hydrogels for protein delivery

dc.contributor.authorMahran Alaa
dc.contributor.authorÖzliseli Ezgi
dc.contributor.authorWang Qingbo
dc.contributor.authorÖzliseli Ilayda
dc.contributor.authorBhadane Rajendra
dc.contributor.authorXu Chunlin
dc.contributor.authorWang Xiaoju
dc.contributor.authorRosenholm Jessica M
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id180795602
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/180795602
dc.date.accessioned2025-08-28T01:30:49Z
dc.date.available2025-08-28T01:30:49Z
dc.description.abstract<p>Multifunctional biomaterial inks are in high demand for adapting hydrogels in biomedical applications through three-dimensional (3D) printing. Our previously developed xeno-free system consisting of anionic cellulose nanofibers (T-CNF) and methacrylated galactoglucomannan (GGMMA) as a photo(bio)polymer provides high-performance ink fidelity in extrusion-based 3D printing. The fusion between nanoparticles and this biomaterial-ink system is a promising yet challenging avenue worth exploring, due to the colloidal stability of T-CNF being sensitive to electrostatic interactions. Mesoporous silica nanoparticles (MSNs), with their robust ceramic matrix and fine-tunable surface chemistries, are well-established nanocarriers for different biologicals. Here, we fabricated MSNs with different surface modifications resulting in a net surface charge ranging from highly negative to highly positive to develop printable MSNs-laden nanocomposite biomaterial inks. We utilized rheology as a comprehensive tool to address the matrix interactions with differently surface-charged MSNs. Fluorescently labeled bovine serum albumin (FITC-BSA) was used as a model protein for MSN loading, whereby negatively or neutral-charged MSNs were found suitable to formulate FITC-BSA-loaded biomaterial inks of T-CNF/GGMMA. Depending on the particles’ surface charge, FITC-BSA showed different release profiles and preserved its stability after release. Lastly, the proof-of-concept to deliver large-sized biological cargo with MSN-laden nanocomposite biomaterial inks was established via the 3D printing technique.<br></p>
dc.identifier.jour-issn2688-4011
dc.identifier.olddbid207649
dc.identifier.oldhandle10024/190676
dc.identifier.urihttps://www.utupub.fi/handle/11111/51112
dc.identifier.urlhttp://dx.doi.org/10.1002/nano.202300097
dc.identifier.urnURN:NBN:fi-fe2025082787741
dc.language.isoen
dc.okm.affiliatedauthorBhadane, Rajendra
dc.okm.discipline221 Nanotechnologyen_GB
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline317 Pharmacyen_GB
dc.okm.discipline221 Nanoteknologiafi_FI
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline317 Farmasiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWiley
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1002/nano.202300097
dc.relation.ispartofjournalNano select
dc.source.identifierhttps://www.utupub.fi/handle/10024/190676
dc.titleSemi‐solid 3D printing of mesoporous silica nanoparticle‐incorporated xeno‐free nanomaterial hydrogels for protein delivery
dc.year.issued2023

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