Hepatocellular carcinoma targeted near-Infrared in vivo imaging by β-galactosidase stimulated fluorescent probe
Abstract
Development of targeted, selective, and noninvasive fluorescent probes for in vivo visualization of tumor-associated over-expressed enzymes are highly anticipated for cancer diagnosis and therapy. Herein, we developed a... [ view full abstract ]
Development of targeted, selective, and noninvasive fluorescent probes for in vivo visualization of tumor-associated over-expressed enzymes are highly anticipated for cancer diagnosis and therapy. Herein, we developed a noninvasive fluorescent probe (DCDHF-βgal) for the sensitive detection, and in vivo visualization of β-galactosidase in hepatocyte HepG2 cells and its xenograft model. As a model system for in vivo targeted imaging, DCDHF-βgal possessing galactose unit selectively target hepatocyte and monitor the β-galactosidase activity with deep tissue penetration, and low background interference. DCDHF-βgal was activated by intracellular β-galactosidases as the driving force for the release of NIR fluorophore, thereby exhibiting ratiometric optical response. Initial fluorescence emission measured at 615 nm was changed to fluorescence at 665 nm upon activation of DCDHF-βgal with β-galactosidase. Ratiometric fluorescence detection of β-galactosidase was also observed in hepatocellular carcinoma cells and tumor xenograft. The noninvasive in vivo optical imaging facilitated by targeted and enzymeactivated imaging agent would be useful in various biomedical and diagnostic applications.
Authors
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Hyun Min Kim
(Korea Basic Science Institute, Korea Research Institute of Bioscience & Biotechnology)
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Hyunseung Lee
(Korea Basic Science Institute, Korea Research Institute of Bioscience & Biotechnology)
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Kwan Soo Hong
(Korea Basic Science Institute, Korea Research Institute of Bioscience & Biotechnology)
Topic Area
Nano-Imaging for diagnosis, therapy and delivery
Session
PS2 » Poster Session (13:30 - Tuesday, 26th September, Gallery)
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