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Updated: Feb 13, 2026

Assessment of Ovarian Cancer Spheroid Attachment and Invasion of Mesothelial Cells in Real Time
Published on: May 20, 2014
β-Galactosidase-Activated Near-Infrared Fluorescence and 1H/19F MRI Trimodal Probe for Real-Time In Vivo Imaging of
Na Li1,2, Long Xiao1, Sha Li1,2
1State Key Laboratory of Magnetic Resonance Spectroscopy and Imaging, National Center for Magnetic Resonance in Wuhan, Wuhan Institute of Physics and Mathematics, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences, Wuhan 430071, P. R. China.
Abstract:
β-Galactosidase (β-gal), overexpressed in primary ovarian tumors, serves as an important biomarker for ovarian cancer. Accurate and sensitive detection of β-gal is crucial for cancer diagnosis and therapy. Activatable multimodal probes that show enhancement of multiplex imaging signals upon interaction with their specific molecular target have become powerful tools for rapid and precise imaging of biological processes. Nevertheless, the rational design of such probes remains challenging. Herein, a novel β-gal-activated probe, named Gal-Cy-Gd-F, was designed and synthesized for trimodal imaging of its activity in vivo. Upon activation by β-gal, the probe underwent a unique quinone methide-mediated self-immobilization mechanism that covalently anchored onto the target enzyme or neighboring proteins, thereby effectively prolonging its retention time. Consequently, the longitudinal relaxivity increased from 8.67 ± 0.5 mM-1 s-1 to 13.85 ± 0.2 mM-1 s-1 in solution under a 0.5 T nuclear magnetic resonance relaxometer, which was 3.7 times higher than commercial Gd-DOTA. Additionally, the fluorescence intensity and 19F magnetic resonance (MR) signal recovery are closely related to the β-gal concentration which can be quantified using the fluorescence method at low concentrations (0.02-0.1 U/mL) and the 19F MR method at high concentrations (0.2-0.8 U/mL), enabling highly sensitive, selective, background-free, and quantitative detection of β-gal activity in vitro. Furthermore, in vivo experiments demonstrated that Gal-Cy-Gd-F enables the precise monitoring of β-gal in mice, resulting in a remarkable increase in fluorescence intensity, a 33% enhancement in 1H MR signal contrast, and significant recovery of 19F MR signal. This platform effectively overcomes the limitations of current ovarian cancer diagnostic methods, providing a powerful tool for early detection, precise intraoperative navigation, and therapeutic monitoring of ovarian cancer.
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