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Optoacoustic Imaging of Glucagon-like Peptide-1 Receptor with a Near-Infrared Exendin-4 Analog.

J Nucl Med · 2021

Last updated 2026-05-28

Researchers developed a new imaging tool called E4-Cy7, which uses near-infrared light to target and visualize cells with GLP-1 receptors, such as those in pancreatic islets. In lab tests, E4-Cy7 showed strong binding ability (with a dissociation constant of 4.6 ± 0.8 nM) and successfully allowed imaging of insulin-producing tumors in live animals for the first time using optoacoustic technology.

AI summary of the abstract below.

JournalJ Nucl Med, 2021
Citations6
Relative citation ratio0.42
NIH percentile25
Molecules

Abstract

Limitations in current imaging tools have long challenged the imaging of small pancreatic islets in animal models. Here, we report the first development and in vivo validation testing of a broad-spectrum and high-absorbance near-infrared optoacoustic contrast agent, E4-Cy7. Our near-infrared tracer is based on the amino acid sequence of exendin-4 and targets the glucagon-like peptide-1 receptor (GLP-1R). Cell assays confirmed that E4-Cy7 has a high-binding affinity (dissociation constant, Kd, 4.6 ± 0.8 nM). Using the multispectral optoacoustic tomography, we imaged E4-Cy7 and optoacoustically visualized β-cell insulinoma xenografts in vivo for the first time. In the future, similar optoacoustic tracers that are specific for β-cells and combines optoacoustic and fluorescence imaging modalities could prove to be important tools for monitoring the pancreas for the progression of diabetes.

Verbatim abstract via PubMed 33097631 ↗