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      Nanoparticles and intracellular applications of surface-enhanced Raman spectroscopy

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          Abstract

          Surface-enhanced Raman spectroscopy offers ultra-sensitive vibrational fingerprinting within biological cells.

          Abstract

          Surface-enhanced Raman spectrocopy (SERS) offers ultrasensitive vibrational fingerprinting at the nanoscale. Its non-destructive nature affords an ideal tool for interrogation of the intracellular environment, detecting the localisation of biomolecules, delivery and monitoring of therapeutics and for characterisation of complex cellular processes at the molecular level. Innovations in nanotechnology have produced a wide selection of novel, purpose-built plasmonic nanostructures capable of high SERS enhancement for intracellular probing while microfluidic technologies are being utilised to reproducibly synthesise nanoparticle (NP) probes at large scale and in high throughput. Sophisticated multivariate analysis techniques unlock the wealth of previously unattainable biomolecular information contained within large and multidimensional SERS datasets. Thus, with suitable combination of experimental techniques and analytics, SERS boasts enormous potential for cell based assays and to expand our understanding of the intracellular environment. In this review we trace the pathway to utilisation of nanomaterials for intracellular SERS. Thus we review and assess nanoparticle synthesis methods, their toxicity and cell interactions before presenting significant developments in intracellular SERS methodologies and how identified challenges can be addressed.

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          Nanoparticle-mediated cellular response is size-dependent.

          Nanostructures of different sizes, shapes and material properties have many applications in biomedical imaging, clinical diagnostics and therapeutics. In spite of what has been achieved so far, a complete understanding of how cells interact with nanostructures of well-defined sizes, at the molecular level, remains poorly understood. Here we show that gold and silver nanoparticles coated with antibodies can regulate the process of membrane receptor internalization. The binding and activation of membrane receptors and subsequent protein expression strongly depend on nanoparticle size. Although all nanoparticles within the 2-100 nm size range were found to alter signalling processes essential for basic cell functions (including cell death), 40- and 50-nm nanoparticles demonstrated the greatest effect. These results show that nanoparticles should no longer be viewed as simple carriers for biomedical applications, but can also play an active role in mediating biological effects. The findings presented here may assist in the design of nanoscale delivery and therapeutic systems and provide insights into nanotoxicity.
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            (CdSe)ZnS Core−Shell Quantum Dots:  Synthesis and Characterization of a Size Series of Highly Luminescent Nanocrystallites

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              Elucidating the mechanism of cellular uptake and removal of protein-coated gold nanoparticles of different sizes and shapes.

              We investigated the mechanism by which transferrin-coated gold nanoparticles (Au NP) of different sizes and shapes entered mammalian cells. We determined that transferrin-coated Au NP entered the cells via clathrin-mediated endocytosis pathway. The NPs exocytosed out of the cells in a linear relationship to size. This was different than the relationship between uptake and size. Furthermore, we developed a mathematical equation to predict the relationship of size versus exocytosis for different cell lines. These studies will provide guidelines for developing NPs for imaging and drug delivery applications, which will require "controlling" NP accumulation rate. These studies will also have implications in determining nanotoxicity.
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                Author and article information

                Journal
                Analyst
                Analyst
                The Analyst
                Royal Society of Chemistry
                0003-2654
                1364-5528
                7 September 2016
                19 July 2016
                : 141
                : 17
                : 5037-5055
                Affiliations
                [a ] Department of Chemistry and Institute of Life Sciences (IfLS) , University of Southampton , SO17 1BJ , UK . Email: s.mahajan@ 123456soton.ac.uk
                [b ] Sector for Biological and Soft Systems , Cavendish Laboratory , Department of Physics , University of Cambridge , 19 JJ Thomson Avenue , Cambridge , CB3 0HE , UK
                [c ] Discovery Sciences , Screening and Compound Management , AstraZeneca , Unit 310 - Darwin Building , Cambridge Science Park , Milton Road , Cambridge , CB4 0WG , UK
                Author notes

                †Current address: Department of Chemistry, School of Chemistry and Molecular Engineering, East Chinal Normal University, 500, Dongchuan Road, Shanghai, 200241, China. E-mail: lli@chem.ecnu.edu.cn

                Article
                c6an01003b
                10.1039/c6an01003b
                5048737
                27479539
                60fdf3cb-8b65-447a-9aed-e5cc33d1bcf1
                This journal is © The Royal Society of Chemistry 2016

                This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License ( http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 29 April 2016
                : 18 July 2016
                Categories
                Chemistry

                Clinical Psychology & Psychiatry
                Clinical Psychology & Psychiatry

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