Amyloids are insoluble fibrous protein aggregates that accumulate in various organs throughout the human body. It has been clinically proven that abnormal accumulation of beta-amyloids in the brain is associated with various neurodegenerative diseases, including Alzheimer disease. Diagnostic biomarkers currently in clinical development are limited to small radio-labeled molecules for detection of amyloidosis through PET or SPECT imaging modes. There remains a pressing need for the design and development of new imaging agents for conclusive early diagnosis of Alzheimer’s disease, ideally through widely accessible detection platforms.
A common structural feature of known amyloid-binding agents is an electronically-polarized, extended aromatic system that is inherent to a family of fluorescent probes known as molecular rotors. Features of molecular rotors, which inherently decrease the non-radiative decay rate and increase fluorescence emission upon binding to aggregated beta-amyloids, were incorporated into a general design of novel, amyloid-binding agents.
Proprietary methods were used to identify, synthesize, and characterize seven, novel compositions of matter. Development included in vitro evaluation for specifications relevant to use in clinical practice, including: solubility, fluorescence characteristics, ability to cross the blood-brain barrier, binding constants, and capability to detect amyloidosis in brain tissue.
US and numerous foreign rights available for licensure in some fields. US application at link, below.
Country | Type | Number | Dated | Case |
United States Of America | Issued Patent | 9,551,722 | 01/24/2017 | 2010-162 |
United States Of America | Issued Patent | 8,940,918 | 01/27/2015 | 2010-162 |
neurodegenerative, Alzheimer, Parkinson, Huntington, arthritis, RA, beta-amyloid, brain, fluoroprobes, emission, fluorescent probe, amyloid, CNS, diagnostic, diagnosis, detection, therapeutic, small molecule, imaging, image, ophthalmology, ophthalmologic