Abstract
Bioimaging probes based on carbon dots (CDs) can become a useful replacement for existing commercial probes, benefiting clinical diagnostics. While the development of dual-mode CD-based probes for magnetic resonance imaging (MRI), which provides the ability for photoluminescence (PL) detection at the same time, is ongoing, several challenges have to be addressed. First, most of the CD-based probes still emit at shorter wavelengths (blue/green spectral range), which is harmful to biological objects or have very low PL intensity in the biological window of tissue transparency (red/near-infrared spectral range). Second, the relaxation characteristics of the proposed CD-based probes are still similar or only slightly larger than those of commercial contrast agents. Herein, we introduce a dual-mode probe allowing for simultaneous PL detection and MRI analysis, based on CDs doped with gadolinium ions (Gd3+) with a PL peak in the red (640 nm), a PL quantum yield up to 24%, and high longitudinal and transverse relaxivities reaching 25.76 and 40.57 L mmol-1 s-1, respectively. Moreover, Gd-doped CDs show good biocompatibility, which was studied on H9c2 and 4T1 cell lines with a cell viability above 70%. The developed Gd-doped red-emissive CDs can be utilized as efficient and nontoxic dual-mode probes for PL and MRI measurements carried out simultaneously. © 2025 American Chemical Society.
| Original language | English |
|---|---|
| Pages (from-to) | 1493-1502 |
| Journal | ACS Applied Bio Materials |
| Volume | 8 |
| Issue number | 2 |
| Online published | 31 Jan 2025 |
| DOIs | |
| Publication status | Published - 17 Feb 2025 |
Research Keywords
- bioimaging
- carbon dots
- gadolinium doping
- MRI contrast agents
- red emission
Publisher's Copyright Statement
- COPYRIGHT TERMS OF DEPOSITED POSTPRINT FILE: This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Bio Materials, copyright © 2025 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsabm.4c01705.
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