Non-destructive in vivo tracking of gelatin hydrogels for advancing tissue engineering
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F25%3A00636587" target="_blank" >RIV/61389013:_____/25:00636587 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11110/25:10499915
Výsledek na webu
<a href="https://www.nature.com/articles/s43246-025-00830-2" target="_blank" >https://www.nature.com/articles/s43246-025-00830-2</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/s43246-025-00830-2" target="_blank" >10.1038/s43246-025-00830-2</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Non-destructive in vivo tracking of gelatin hydrogels for advancing tissue engineering
Popis výsledku v původním jazyce
Photo-crosslinkable gelatin-based hydrogels hold great promise for tissue engineering and regenerative medicine. However, monitoring these hydrogels in vivo remains challenging and limits their further development and clinical translation. Here, we address this limitation by utilizing a gelatin-based hydrogel that incorporates the radiopaque compound 5-acrylamido-2,4,6-triiodoisophthalic acid (AATIPA). In an in vivo study spanning over 400 days, we monitor the degradation kinetics of these hydrogels using computed tomography and ultrasonography. We synthesize three distinct AATIPA-containing hydrogels and implant them subcutaneously into mice. Hydrogels with high crosslink density show minimal degradation, while those with lower crosslinking densities degrade within approximately three months. Histological evaluation reveals that the scaffolds are replaced by adjacent adipose tissue. In vitro, adipose-derived stem cells differentiate into the adipogenic lineage, corroborating the in vivo findings. These results highlight the potential of these hydrogels for adipose tissue engineering by enabling in vivo monitoring and offering tailored degradation profiles.
Název v anglickém jazyce
Non-destructive in vivo tracking of gelatin hydrogels for advancing tissue engineering
Popis výsledku anglicky
Photo-crosslinkable gelatin-based hydrogels hold great promise for tissue engineering and regenerative medicine. However, monitoring these hydrogels in vivo remains challenging and limits their further development and clinical translation. Here, we address this limitation by utilizing a gelatin-based hydrogel that incorporates the radiopaque compound 5-acrylamido-2,4,6-triiodoisophthalic acid (AATIPA). In an in vivo study spanning over 400 days, we monitor the degradation kinetics of these hydrogels using computed tomography and ultrasonography. We synthesize three distinct AATIPA-containing hydrogels and implant them subcutaneously into mice. Hydrogels with high crosslink density show minimal degradation, while those with lower crosslinking densities degrade within approximately three months. Histological evaluation reveals that the scaffolds are replaced by adjacent adipose tissue. In vitro, adipose-derived stem cells differentiate into the adipogenic lineage, corroborating the in vivo findings. These results highlight the potential of these hydrogels for adipose tissue engineering by enabling in vivo monitoring and offering tailored degradation profiles.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10404 - Polymer science
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Communications Materials
ISSN
2662-4443
e-ISSN
2662-4443
Svazek periodika
6
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
11
Strana od-do
112
Kód UT WoS článku
001507086900001
EID výsledku v databázi Scopus
2-s2.0-105007156091