Coordination chemistry of ligands: insights into the design of amyloid beta/tau-PET imaging probes and nanoparticles-based therapies for Alzheimer's disease

The diagnosis and therapy of neurodegenerative diseases are highly indispensable. In particular, the definitive clinical diagnosis and therapy of Alzheimer's disease (AD) remains a challenge. Despite the use of amyloid beta (Aβ) positron emission tomography (PET) gold standard [11C]-PiB, other approved benzothiazole ([18F]-flutemetamol) and stilbene derivative ([18F]-florbetaben and [18F]-florbetapir) based probes have been extensively studied and advocated as potential early Aβ PET radioligands for AD. Recent years have witnessed a burgeoning research activity in the development of radiotracers for tau neurofibrillary tangles (NFTs) binding using PET imaging, while monitoring the progression of disease. Notably, several tau PET ligands (e.g. [18F]-THK5351, [18F]-MK-6240, and [18F]-AV-1451, [18F]-RO-6958948, [18F]-JNJ-64326067, [18F]-PI-2620) showed high affinity and selective binding to tau pathology. Although early detection and progression of AD have been studied extensively using PET imaging, therapeutic approaches to the disease are scarce. Recently, nanoparticles (NPs) based therapeutic approaches have emerged. Coordination of ligands to the surface of organic NPs (e.g., flavonoids: green tea polyphenol- EGCG, curcumin), and inorganic NPs (e.g. Au, ZnO, CeO2) have been explored to decrease/inhibit the amyloid aggregation and tau hyperphosphorylation. This review focuses on (i) the importance of coordination chemistry of ligands in the design of PET imaging probes with specific binding affinities to Aβ and tau NFTs in AD, and (ii) the role of surface ligands and their coordination to NPs and functional molecules for the rational design of novel anti-AD reagents for therapeutic interventions.Nanyang Technological UniversityS.T.S., B.G., P.P. thank the support from Lee Kong Chian School of Medicine, Imaging Probe Development Platform, and Cognitive Neuro Imaging Centre (CONIC) at Nanyang Technological University (NTU) Singapore

Theranostic Probes for Targeting Tumor Microenvironment: An Overview

Long gone is the time when tumors were thought to be insular masses of cells, residing independently at specific sites in an organ. Now, researchers gradually realize that tumors interact with the extracellular matrix (ECM), blood vessels, connective tissues, and immune cells in their environment, which is now known as the tumor microenvironment (TME). It has been found that the interactions between tumors and their surrounds promote tumor growth, invasion, and metastasis. The dynamics and diversity of TME cause the tumors to be heterogeneous and thus pose a challenge for cancer diagnosis, drug design, and therapy. As TME is significant in enhancing tumor progression, it is vital to identify the different components in the TME such as tumor vasculature, ECM, stromal cells, and the lymphatic system. This review explores how these significant factors in the TME, supply tumors with the required growth factors and signaling molecules to proliferate, invade, and metastasize. We also examine the development of TME-targeted nanotheranostics over the recent years for cancer therapy, diagnosis, and anticancer drug delivery systems. This review further discusses the limitations and future perspective of nanoparticle based theranostics when used in combination with current imaging modalities like Optical Imaging, Magnetic Resonance Imaging (MRI) and Nuclear Imaging (Positron Emission Tomography (PET) and Single Photon Emission Computer Tomography (SPECT)).MOE (Min. of Education, S’pore)Published versio