Semi‐solid 3D printing of mesoporous silica nanoparticle‐incorporated xeno‐free nanomaterial hydrogels for protein delivery
| dc.contributor.author | Mahran Alaa | |
| dc.contributor.author | Özliseli Ezgi | |
| dc.contributor.author | Wang Qingbo | |
| dc.contributor.author | Özliseli Ilayda | |
| dc.contributor.author | Bhadane Rajendra | |
| dc.contributor.author | Xu Chunlin | |
| dc.contributor.author | Wang Xiaoju | |
| dc.contributor.author | Rosenholm Jessica M | |
| dc.contributor.organization | fi=biolääketieteen laitos|en=Institute of Biomedicine| | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.77952289591 | |
| dc.converis.publication-id | 180795602 | |
| dc.converis.url | https://research.utu.fi/converis/portal/Publication/180795602 | |
| dc.date.accessioned | 2025-08-28T01:30:49Z | |
| dc.date.available | 2025-08-28T01:30:49Z | |
| 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-issn | 2688-4011 | |
| dc.identifier.olddbid | 207649 | |
| dc.identifier.oldhandle | 10024/190676 | |
| dc.identifier.uri | https://www.utupub.fi/handle/11111/51112 | |
| dc.identifier.url | http://dx.doi.org/10.1002/nano.202300097 | |
| dc.identifier.urn | URN:NBN:fi-fe2025082787741 | |
| dc.language.iso | en | |
| dc.okm.affiliatedauthor | Bhadane, Rajendra | |
| dc.okm.discipline | 221 Nanotechnology | en_GB |
| dc.okm.discipline | 3111 Biomedicine | en_GB |
| dc.okm.discipline | 317 Pharmacy | en_GB |
| dc.okm.discipline | 221 Nanoteknologia | fi_FI |
| dc.okm.discipline | 3111 Biolääketieteet | fi_FI |
| dc.okm.discipline | 317 Farmasia | fi_FI |
| dc.okm.internationalcopublication | international co-publication | |
| dc.okm.internationality | International publication | |
| dc.okm.type | A1 ScientificArticle | |
| dc.publisher | Wiley | |
| dc.publisher.country | Germany | en_GB |
| dc.publisher.country | Saksa | fi_FI |
| dc.publisher.country-code | DE | |
| dc.relation.doi | 10.1002/nano.202300097 | |
| dc.relation.ispartofjournal | Nano select | |
| dc.source.identifier | https://www.utupub.fi/handle/10024/190676 | |
| dc.title | Semi‐solid 3D printing of mesoporous silica nanoparticle‐incorporated xeno‐free nanomaterial hydrogels for protein delivery | |
| dc.year.issued | 2023 |
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