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Longitudinal monitoring of nanofibrillar cellulose hydrogel medical implants in mice using positron emission tomography
Tekijät: Zhuang, Xiaoqing; Virta, Jenni; Liljenbäck, Heidi; Paasonen, Lauri; Airaksinen, Anu J.; Roivainen, Anne; Li, Xiang-Guo
Kustantaja: Elsevier
Julkaisuvuosi: 2025
Lehti: European Journal of Pharmaceutical Sciences
Artikkelin numero: 107402
Vuosikerta: 217
ISSN: 0928-0987
eISSN: 1879-0720
DOI: https://doi.org/10.1016/j.ejps.2025.107402
Julkaisun avoimuus kirjaamishetkellä: Avoimesti saatavilla
Julkaisukanavan avoimuus : Kokonaan avoin julkaisukanava
Verkko-osoite: https://doi.org/10.1016/j.ejps.2025.107402
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/505885289
Nanofibrillar cellulose (NFC) hydrogel has emerged as a promising implantable material for therapeutic applications. In this study, the relatively longer-lived positron-emitting radionuclide zirconium-89 was chelated to the octadentate deferoxamine (DFO*)-conjugated NFC hydrogel ([89Zr]Zr-DFO*-NFC) to enable longitudinal monitoring of its in vivo fate using positron emission tomography techniques. Following subcutaneous implantation in healthy mice, [89Zr]Zr-DFO*-NFC retained radioactivity at the implant site for at least 14 days, with minimal signal detected in the kidneys, urinary bladder, and overlying skin. In contrast, mice receiving a control formulation of [89Zr]Zr-oxalate mixed with NFC hydrogel showed progressive accumulation of radioactivity in the bones, consistent with known [89Zr]Zr-oxalate distribution patterns, and only limited retention at the implant site by Day 7. These findings demonstrate that [89Zr]Zr-DFO*-NFC hydrogel implants exhibit high in vivo stability with negligible systemic release following subcutaneous implantation, supporting their potential use as safe and traceable biomaterial platforms.
Ladattava julkaisu This is an electronic reprint of the original article. |
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This work was supported by research funding from UPM Biomedicals, Helsinki, Finland.