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      Nanoparticle Functionalization and Its Potentials for Molecular Imaging

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          Abstract

          Functionalization enhances the properties and characteristics of nanoparticles through surface modification, and enables them to play a major role in the field of medicine. In molecular imaging, quality functional images are required with proper differentiation which can be seen with high contrast to obtain viable information. This review article discusses how functionalization enhances molecular imaging and enables multimodal imaging by which images with combination of functions particular to each modality can be obtained. This also explains how nanoparticles interacting at molecular level, when functionalized with molecules can target the cells of interest or substances with high specificity, reducing background signal and allowing simultaneous therapies to be carried out while imaging. Functionalization allows imaging for a prolonged period and enables to track the cells over a period of time. Recent researches and progress in functionalizing the nanoparticles to specifically enhance bioimaging with different modalities and their applications are reviewed in this article.

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          Most cited references89

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          The enhanced permeability and retention (EPR) effect in tumor vasculature: the key role of tumor-selective macromolecular drug targeting.

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            Photoluminescence-tunable carbon nanodots: surface-state energy-gap tuning.

            The photoluminescence of carbon nanodots (C-dots) can be tuned by changing their surface chemistry or size because the photoluminescence is a function of the surface-state electronic transitions. Increasing the degree of surface oxidation leads to a narrowing of the energy gap of the surface; meanwhile, larger C-dots with an extensive π-electron system, which can couple with surface electronic states, can also lead to a narrowing of the energy gap of the surface states.
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              In vivo tumor targeting and image-guided drug delivery with antibody-conjugated, radiolabeled mesoporous silica nanoparticles.

              Since the first use of biocompatible mesoporous silica (mSiO2) nanoparticles as drug delivery vehicles, in vivo tumor targeted imaging and enhanced anticancer drug delivery has remained a major challenge. In this work, we describe the development of functionalized mSiO2 nanoparticles for actively targeted positron emission tomography (PET) imaging and drug delivery in 4T1 murine breast tumor-bearing mice. Our structural design involves the synthesis, surface functionalization with thiol groups, PEGylation, TRC105 antibody (specific for CD105/endoglin) conjugation, and (64)Cu-labeling of uniform 80 nm sized mSiO2 nanoparticles. Systematic in vivo tumor targeting studies clearly demonstrated that (64)Cu-NOTA-mSiO2-PEG-TRC105 could accumulate prominently at the 4T1 tumor site via both the enhanced permeability and retention effect and TRC105-mediated binding to tumor vasculature CD105. As a proof-of-concept, we also demonstrated successful enhanced tumor targeted delivery of doxorubicin (DOX) in 4T1 tumor-bearing mice after intravenous injection of DOX-loaded NOTA-mSiO2-PEG-TRC105, which holds great potential for future image-guided drug delivery and targeted cancer therapy.
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                Author and article information

                Contributors
                ppadmanabhan@ntu.edu.sg
                balazs.gulyas@ntu.edu.sg
                Journal
                Adv Sci (Weinh)
                Adv Sci (Weinh)
                10.1002/(ISSN)2198-3844
                ADVS
                Advanced Science
                John Wiley and Sons Inc. (Hoboken )
                2198-3844
                16 December 2016
                March 2017
                : 4
                : 3 ( doiID: 10.1002/advs.v4.3 )
                : 1600279
                Affiliations
                [ 1 ] Lee Kong Chian School of MedicineNanyang Technological University 59 Nanyang Drive 636921Singapore
                [ 2 ] Center for Biotechnology Alagappa College of TechnologyAnna University Sardar Patel Road Chennai Tamil Nadu 600025India
                Author notes
                Article
                ADVS257
                10.1002/advs.201600279
                5357986
                28331783
                934944b8-e0e6-4516-aff3-c4cc28992b9e
                © 2016 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 July 2016
                : 02 October 2016
                Page count
                Figures: 12, Tables: 1, Pages: 14, Words: 9953
                Funding
                Funded by: Lee Kong Chian School of Medicine
                Funded by: Nanyang Technological University
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                advs257
                March 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.0.8 mode:remove_FC converted:20.03.2017

                conjugation,functionalization,imaging,microscopy,nanoparticles

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