Mesoporous Silica-Coated Gold Nanoparticles for Multimodal Imaging and Reactive Oxygen Species Sensing of Stem Cells

Autor: Chloe Trayford, Darragh Crosbie, Timo Rademakers, Clemens van Blitterswijk, Rudy Nuijts, Stefano Ferrari, Pamela Habibovic, Vanessa LaPointe, Mor Dickman, Sabine van Rijt
Přispěvatelé: Division Instructive Biomaterials Eng, RS: MERLN - Instructive Biomaterials Engineering (IBE), CBITE, RS: MERLN - Cell Biology - Inspired Tissue Engineering (CBITE), CTR, RS: MERLN - Complex Tissue Regeneration (CTR), MUMC+: *AB Refractie Chirurgie Oogheelkunde (9), Oogheelkunde, MUMC+: MA UECM Oogartsen MUMC (9), RS: MHeNs - R3 - Neuroscience, MUMC+: MA UECM Oogartsen ZL (9), MUMC+: MA UECM AIOS (9)
Rok vydání: 2022
Předmět:
Zdroj: ACS Applied Nano Materials, 5(3), 3237-3251. American Chemical Society
ISSN: 2574-0970
Popis: Stem cell (SC)-based therapies hold the potential to revolutionize therapeutics by enhancing the body's natural repair processes. Currently, there are only three SC therapies with marketing authorization within the European Union. To optimize outcomes, it is important to understand the biodistribution and behavior of transplanted SCs in vivo. A variety of imaging agents have been developed to trace SCs; however, they mostly lack the ability to simultaneously monitor the SC function and biodistribution at high resolutions. Here, we report the synthesis and application of a nanoparticle (NP) construct consisting of a gold NP core coated with rhodamine B isothiocyanate (RITC)-doped mesoporous silica (AuMS). The MS layer further contained a thiol-modified internal surface and an amine-modified external surface for dye conjugation. Highly fluorescent AuMS of three different sizes were successfully synthesized. The NPs were non-toxic and efficiently taken up by limbal epithelial SCs (LESCs). We further showed that we can functionalize AuMS with a reactive oxygen species (ROS)-sensitive fluorescent dye using two methods, loading the probe into the mesopores, with or without additional capping by a lipid bilayer, and by covalent attachment to surface and/or mesoporous-functionalized thiol groups. All four formulations displayed a ROS concentration-dependent increase in fluorescence. Further, in an ex vivo SC transplantation model, a combination of optical coherence tomography and fluorescence microscopy was used to synergistically identify AuMS-labeled LESC distribution at micrometer resolution. Our AuMS constructs allow for multimodal imaging and simultaneous ROS sensing of SCs and represent a promising tool for in vivo SC tracing.
Databáze: OpenAIRE