Paper
2 February 2012 Self-illuminating nanoprobe for in vivo imaging of cancers over-expressing the folate receptor
Steven C. Miller, Lucia Beviglia, Pete Yeung, Sukanta Bhattacharyya, Daniel Sobek
Author Affiliations +
Abstract
New in vivo imaging reagents with increased sensitivity and penetration depth are needed to advance our understanding of metastases and accelerate the development of therapeutics. The folate receptor (FR) is a promising imaging target that is up-regulated in many human carcinomas, including cancers of the ovary, breast, pancreas, endometrium, lungs, kidneys, colon, brain, and myeloid cells. Zymera has developed a self-illuminating Bioluminescence Resonance Energy Transfer Quantum Dot (BRET-Qdot) nanoprobe conjugated with folate (BQ-Folate) for in vivo imaging of cancers overexpressing FR. BQ-Folate is a novel nanoprobe formed by co-conjugating Renilla reniformis luciferase enzyme and folate to near-infrared (NIR) emitting quantum dots. The luciferase substrate, coelenterazine, activates the BQ-Folate nanoprobe generating luminescence emission in the near-infrared (NIR) region (655 nm) for increased sensitivity and penetration depth. Because BQ-Folate requires no external light source for light emission, it has significant advantages for challenging in vivo preclinical optical imaging applications, such as the detection of early stage metastases. Zymera and OncoMed Pharmaceuticals have demonstrated that in vivo imaging with the BQ-Folate nanoprobe detected the primary tumor and early stage metastases in an orthotopic NOD/SCID mouse model of human pancreatic cancer.
© (2012) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Steven C. Miller, Lucia Beviglia, Pete Yeung, Sukanta Bhattacharyya, and Daniel Sobek "Self-illuminating nanoprobe for in vivo imaging of cancers over-expressing the folate receptor", Proc. SPIE 8233, Reporters, Markers, Dyes, Nanoparticles, and Molecular Probes for Biomedical Applications IV, 82330Z (2 February 2012); https://doi.org/10.1117/12.909379
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Cited by 1 scholarly publication.
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KEYWORDS
Tumors

In vivo imaging

Nanoprobes

Cancer

Pancreatic cancer

Receptors

Bioluminescence

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