Current diagnostic approaches to neurodegenerative diseases are often flawed as they are often invasive and cannot effectively diagnose early-onset dementia. Antibody-based therapeutics for neurodegenerative diseases are very promising but often lack specificity to certain biomarkers and require invasive methods of administration such as a lumbar puncture. In this study I report a novel quantum-dot (QD) conjugated bispecific-antibody (BsAb) diagnosis system designed for Alzheimer’s disease. This structure is easy to synthesize and displays specificity to oligomeric amyloid-beta (Aβ), which is often present before Alzheimer’s symptoms starts to manifest. The bispecific antibody also binds with a weak affinity to transferrin receptors – thus potentially allowing it to cross the blood-brain barrier (BBB) via receptor-mediated transcytosis and reducing the necessity for extremely- invasive means of administration such as a lumbar puncture. The CdTe/ZnS QDs conjugated to the BsAb have multimodal, non-invasive MRI and fNIR imaging capabilities and also displayed allow cytotoxicity to neuronal cells. The synthesized nanoparticles composed of CdTe/ZnS with a Gd-DOTA doped silica shell also displayed therapeutic properties by immobilizing the toxic oligomeric Aβ and increasing neuronal viability. These novel BsAb-QD structures display promising diagnostic and therapeutic properties and represent an important evolution in neurodegenerative drug design.
I synthesized a novel nanoparticle-bound antibody for the earlier diagnosis and treatment of Alzheimer’s disease which proves to be less invasive and more accurate in comparison to existing tests of its kind.