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Molecular Engineering of Self-Immolative Bioresponsive MR Probes.
- Source :
-
Journal of the American Chemical Society [J Am Chem Soc] 2023 May 10; Vol. 145 (18), pp. 10045-10050. Date of Electronic Publication: 2023 Apr 28. - Publication Year :
- 2023
-
Abstract
- Real-time detection of bio-event in whole animals provides essential information for understanding biological and therapeutic processes. Magnetic resonance (MR) imaging represents a non-invasive approach to generating three-dimensional anatomic images with high spatial-temporal resolution and unlimited depth penetration. We have developed several self-immolative enzyme-activatable agents that provide excellent in vivo contrast and function as gene expression reporters. Here, we describe a vast improvement in image contrast over our previous generations of these bioresponsive agents based on a new pyridyl-carbamate Gd(III) complex. The pyridyl-carbamate-based agent has a very low MR relaxivity in the "off-state" ( r <subscript>1</subscript> = 1.8 mM <superscript>-1</superscript> s <superscript>-1</superscript> at 1.41 T). However, upon enzymatic processing, it generates a significantly higher relaxivity with a Δ r <subscript>1</subscript> = 106% versus Δ r <subscript>1</subscript> ∼ 20% reported previously. Single X-ray crystal and nuclear magnetic relaxation dispersion analyses offer mechanistic insights regarding MR signal enhancement at the molecular scale. This work demonstrates a pyridyl-carbamate-based self-immolative molecular platform for the construction of enzymatic bio-responsive MR agents, which can be adapted to a wide range of other targets for exploring stimuli-responsive materials and biomedical applications.
- Subjects :
- Animals
Contrast Media chemistry
Magnetic Resonance Imaging methods
Magnetics
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5126
- Volume :
- 145
- Issue :
- 18
- Database :
- MEDLINE
- Journal :
- Journal of the American Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- 37116079
- Full Text :
- https://doi.org/10.1021/jacs.2c13672