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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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            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

                Journal
                Adv Sci (Weinh)
                Advanced science (Weinheim, Baden-Wurttemberg, Germany)
                Wiley
                2198-3844
                2198-3844
                Mar 2017
                : 4
                : 3
                Affiliations
                [1 ] Lee Kong Chian School of Medicine Nanyang Technological University 59 Nanyang Drive 636921 Singapore; Center for Biotechnology Alagappa College of Technology Anna University Sardar Patel Road Chennai Tamil Nadu 600025 India.
                [2 ] Lee Kong Chian School of Medicine Nanyang Technological University 59 Nanyang Drive 636921 Singapore.
                [3 ] Center for Biotechnology Alagappa College of Technology Anna University Sardar Patel Road Chennai Tamil Nadu 600025 India.
                Article
                ADVS257
                10.1002/advs.201600279
                5357986
                28331783
                934944b8-e0e6-4516-aff3-c4cc28992b9e
                History

                microscopy,conjugation,functionalization,imaging,nanoparticles

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