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      Renal clearable catalytic gold nanoclusters for in vivo disease monitoring

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          Abstract

          Ultra-small gold nanoclusters (AuNCs) have emerged as agile probes for in vivo imaging, as they exhibit exceptional tumour accumulation and efficient renal clearance properties. However, their intrinsic catalytic activity, which can enable increased detection sensitivity, has yet to be explored for in vivo sensing. By exploiting the peroxidase-mimicking activity of AuNCs and the precise nanometer size filtration of the kidney, we designed multifunctional protease nanosensors that respond to disease microenvironments to produce a direct colorimetric urinary readout of disease state in less than 1 h. We monitored the catalytic activity of AuNCs in collected urine of a mouse model of colorectal cancer where tumour-bearing mice showed a 13-fold increase in colorimetric signal compared to healthy mice. Nanosensors were eliminated completely through hepatic and renal excretion within 4 weeks after injection with no evidence of toxicity. We envision that this modular approach will enable rapid detection of a diverse range of diseases by exploiting their specific enzymatic signatures.

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          Most cited references31

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          Analysis of nanoparticle delivery to tumours

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            Atomically Precise Colloidal Metal Nanoclusters and Nanoparticles: Fundamentals and Opportunities.

            Colloidal nanoparticles are being intensely pursued in current nanoscience research. Nanochemists are often frustrated by the well-known fact that no two nanoparticles are the same, which precludes the deep understanding of many fundamental properties of colloidal nanoparticles in which the total structures (core plus surface) must be known. Therefore, controlling nanoparticles with atomic precision and solving their total structures have long been major dreams for nanochemists. Recently, these goals are partially fulfilled in the case of gold nanoparticles, at least in the ultrasmall size regime (1-3 nm in diameter, often called nanoclusters). This review summarizes the major progress in the field, including the principles that permit atomically precise synthesis, new types of atomic structures, and unique physical and chemical properties of atomically precise nanoparticles, as well as exciting opportunities for nanochemists to understand very fundamental science of colloidal nanoparticles (such as the stability, metal-ligand interfacial bonding, ligand assembly on particle surfaces, aesthetic structural patterns, periodicities, and emergence of the metallic state) and to develop a range of potential applications such as in catalysis, biomedicine, sensing, imaging, optics, and energy conversion. Although most of the research activity currently focuses on thiolate-protected gold nanoclusters, important progress has also been achieved in other ligand-protected gold, silver, and bimetal (or alloy) nanoclusters. All of these types of unique nanoparticles will bring unprecedented opportunities, not only in understanding the fundamental questions of nanoparticles but also in opening up new horizons for scientific studies of nanoparticles.
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              From aggregation-induced emission of Au(I)-thiolate complexes to ultrabright Au(0)@Au(I)-thiolate core-shell nanoclusters.

              A fundamental understanding of the luminescence of Au-thiolate nanoclusters (NCs), such as the origin of emission and the size effect in luminescence, is pivotal to the development of efficient synthesis routes for highly luminescent Au NCs. This paper reports an interesting finding of Au(I)-thiolate complexes: strong luminescence emission by the mechanism of aggregation-induced emission (AIE). The AIE property of the complexes was then used to develop a simple one-pot synthesis of highly luminescent Au-thiolate NCs with a quantum yield of ~15%. Our key strategy was to induce the controlled aggregation of Au(I)-thiolate complexes on in situ generated Au(0) cores to form Au(0)@Au(I)-thiolate core-shell NCs where strong luminescence was generated by the AIE of Au(I)-thiolate complexes on the NC surface. We were able to extend the synthetic strategy to other thiolate ligands with added functionalities (in the form of custom-designed peptides). The discovery (e.g., identifying the source of emission and the size effect in luminescence) and the synthesis protocols in this study can contribute significantly to better understanding of these new luminescence probes and the development of new synthetic routes.
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                Author and article information

                Journal
                101283273
                34218
                Nat Nanotechnol
                Nat Nanotechnol
                Nature nanotechnology
                1748-3387
                1748-3395
                12 February 2020
                02 September 2019
                September 2019
                02 September 2020
                : 14
                : 9
                : 883-890
                Affiliations
                [1. ] Department of Materials, Department of Bioengineering, and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, London, U.K.
                [2. ] Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139
                [3. ] Harvard Graduate Program in Biophysics, Harvard University, Boston, MA 02115
                [4. ] Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139
                [5. ] Harvard-MIT Division of Health Sciences and Technology, Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA 02139
                [6. ] Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA 02139
                [7. ] Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA 02115
                [8. ] Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, MA 02139
                [9. ] Howard Hughes Medical Institute, Cambridge, MA 02139
                Author notes
                [†]

                Contributed equally

                Author contributions

                C.N.L., A.P.S., J.S.D., S.N.B., and M.M.S. conceived and designed the research. C.N.L. and A.P.S. carried out all experiments and analysed the data. Y.L. assisted with peptide synthesis and characterization, A.N. performed FCS measurements and analysis, A.B. assisted with ICP-MS, and Q.C. assisted with TEM imaging. C.N.L., A.P.S., S.N.B., and M.M.S. wrote the manuscript with feedback from all authors. C.N.L. and A.P.S. contributed equally, and S.N.B. and M.M.S. are joint corresponding authors.

                [* ] Correspondence and requests for materials should be addressed to S.N.B. and M.M.S. sbhatia@ 123456mit.edu and m.stevens@ 123456imperial.ac.uk
                Article
                PMC7045344 PMC7045344 7045344 nihpa1062497
                10.1038/s41565-019-0527-6
                7045344
                31477801
                07b320a1-1f02-4857-aee4-e238f8100da7
                History
                Categories
                Article

                urinary diagnostic,nanosensors,proteases,activity-based biomarkers,renal clearance,enzyme-mimic,biosensing,nanoclusters,catalytic nanoparticles

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