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      Large-Pore Functionalized Mesoporous Silica Nanoparticles as Drug Delivery Vector for a Highly Cytotoxic Hybrid Platinum-Acridine Anticancer Agent

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          Most cited references51

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          Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism

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            Functionalized mesoporous silica materials for controlled drug delivery.

            In the past decade, non-invasive and biocompatible mesoporous silica materials as efficient drug delivery systems have attracted special attention. Great progress in structure control and functionalization (magnetism and luminescence) design has been achieved for biotechnological and biomedical applications. This review highlights the most recent research progress on silica-based controlled drug delivery systems, including: (i) pure mesoporous silica sustained-release systems, (ii) magnetism and/or luminescence functionalized mesoporous silica systems which integrate targeting and tracking abilities of drug molecules, and (iii) stimuli-responsive controlled release systems which are able to respond to environmental changes, such as pH, redox potential, temperature, photoirradiation, and biomolecules. Although encouraging and potential developments have been achieved, design and mass production of novel multifunctional carriers, some practical biological application, such as biodistribution, the acute and chronic toxicities, long-term stability, circulation properties and targeting efficacy in vivo are still challenging. This journal is © The Royal Society of Chemistry 2012
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              Stimuli-responsive controlled-release delivery system based on mesoporous silica nanorods capped with magnetic nanoparticles.

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                Author and article information

                Journal
                Chemistry - A European Journal
                Chem. Eur. J.
                Wiley
                09476539
                March 08 2017
                March 08 2017
                February 14 2017
                : 23
                : 14
                : 3386-3397
                Affiliations
                [1 ]Department of Chemistry; Wake Forest University; Winston-Salem NC 27109 USA
                [2 ]Department of Cancer Biology; Wake Forest School of Medicine; Winston-Salem NC 27157 USA
                [3 ]Analytical Instrumentation Facility, Monteith Research Center; North Carolina State University; Raleigh NC 27695 USA
                [4 ]Department of Biology; Wake Forest University; Winston-Salem NC 27109 USA
                Article
                10.1002/chem.201604868
                b70d58a1-951f-4c5c-9527-f40e7e26014d
                © 2017

                http://doi.wiley.com/10.1002/tdm_license_1

                http://onlinelibrary.wiley.com/termsAndConditions

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