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

被引:18
作者
Trayford, Chloe [1 ]
Crosbie, Darragh [1 ]
Rademakers, Timo [1 ]
van Blitterswijk, Clemens [1 ]
Nuijts, Rudy [2 ]
Ferrari, Stefano [3 ]
Habibovic, Pamela [1 ]
LaPointe, Vanessa [1 ]
Dickman, Mor [1 ,2 ]
van Rijt, Sabine [1 ]
机构
[1] Maastricht Univ, MERLN Inst Technol Inspired Regenerat Med, NL-6200 MD Maastricht, Netherlands
[2] Univ Eye Clin Maastricht, Univ Med Ctr, Dept Ophthalmol, NL-6202 AZ Maastricht, Netherlands
[3] Fdn Banca Occhi Veneto, I-30174 Venice, Italy
关键词
multimodal imaging; mesoporous silica nanoparticle; gold nanoparticle; stem cell tracing; reactive oxygen species; UP-CONVERSION NANOPARTICLES; IN-VIVO TRACKING; HYDROGEN-PEROXIDE; CELLULAR UPTAKE; SIZE; DRUG; PROBES; MITOCHONDRIA; EFFICIENCY; MECHANISM;
D O I
10.1021/acsanm.1c03640
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:3237 / 3251
页数:15
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