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Longitudinal monitoring of nanofibrillar cellulose hydrogel medical implants in mice using positron emission tomography




TekijätZhuang, Xiaoqing; Virta, Jenni; Liljenbäck, Heidi; Paasonen, Lauri; Airaksinen, Anu J.; Roivainen, Anne; Li, Xiang-Guo

KustantajaElsevier

Julkaisuvuosi2025

Lehti: European Journal of Pharmaceutical Sciences

Artikkelin numero107402

Vuosikerta217

ISSN0928-0987

eISSN1879-0720

DOIhttps://doi.org/10.1016/j.ejps.2025.107402

Julkaisun avoimuus kirjaamishetkelläAvoimesti saatavilla

Julkaisukanavan avoimuus Kokonaan avoin julkaisukanava

Verkko-osoitehttps://doi.org/10.1016/j.ejps.2025.107402

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/505885289


Tiivistelmä

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.
This reprint may differ from the original in pagination and typographic detail. Please cite the original version.




Julkaisussa olevat rahoitustiedot
This work was supported by research funding from UPM Biomedicals, Helsinki, Finland.


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