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      Multifunctional quantum dot DNA hydrogels

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          Abstract

          Biotemplated nanomaterials offer versatile functionality for multimodal imaging, biosensing, and drug delivery. There remains an unmet need for traceable and biocompatible nanomaterials that can be synthesized in a precisely controllable manner. Here, we report self-assembled quantum dot DNA hydrogels that exhibit both size and spectral tunability. We successfully incorporate DNA-templated quantum dots with high quantum yield, long-term photostability, and low cytotoxicity into a hydrogel network in a single step. By leveraging DNA-guided interactions, we introduce multifunctionality for a variety of applications, including enzyme-responsive drug delivery and cell-specific targeting. We report that quantum dot DNA hydrogels can be used for delivery of doxorubicin, an anticancer drug, to increase potency 9-fold against cancer cells. This approach also demonstrated high biocompatibility, trackability, and in vivo therapeutic efficacy in mice bearing xenografted breast cancer tumors. This work paves the way for the development of new tunable biotemplated nanomaterials with multiple synergistic functionalities for biomedical applications.

          Abstract

          The development of nanomaterials for imaging and drug delivery has been of great interest to the field. Here, the authors synthesized multifunctional enzyme-responsive hydrogels with self-assembling quantum dots for nucleic acid and drug delivery as well as having imaging capability.

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          Most cited references39

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          Experimental Determination of the Extinction Coefficient of CdTe, CdSe, and CdS Nanocrystals

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            Nanomaterials. Programmable materials and the nature of the DNA bond.

            For over half a century, the biological roles of nucleic acids as catalytic enzymes, intracellular regulatory molecules, and the carriers of genetic information have been studied extensively. More recently, the sequence-specific binding properties of DNA have been exploited to direct the assembly of materials at the nanoscale. Integral to any methodology focused on assembling matter from smaller pieces is the idea that final structures have well-defined spacings, orientations, and stereo-relationships. This requirement can be met by using DNA-based constructs that present oriented nanoscale bonding elements from rigid core units. Here, we draw analogy between such building blocks and the familiar chemical concepts of "bonds" and "valency" and review two distinct but related strategies that have used this design principle in constructing new configurations of matter.
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              Immunofluorescent labeling of cancer marker Her2 and other cellular targets with semiconductor quantum dots.

              Semiconductor quantum dots (QDs) are among the most promising emerging fluorescent labels for cellular imaging. However, it is unclear whether QDs, which are nanoparticles rather than small molecules, can specifically and effectively label molecular targets at a subcellular level. Here we have used QDs linked to immunoglobulin G (IgG) and streptavidin to label the breast cancer marker Her2 on the surface of fixed and live cancer cells, to stain actin and microtubule fibers in the cytoplasm, and to detect nuclear antigens inside the nucleus. All labeling signals are specific for the intended targets and are brighter and considerably more photostable than comparable organic dyes. Using QDs with different emission spectra conjugated to IgG and streptavidin, we simultaneously detected two cellular targets with one excitation wavelength. The results indicate that QD-based probes can be very effective in cellular imaging and offer substantial advantages over organic dyes in multiplex target detection.
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                Author and article information

                Contributors
                ted.sargent@utoronto.ca
                shana.kelley@utoronto.ca
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                29 August 2017
                29 August 2017
                2017
                : 8
                : 381
                Affiliations
                [1 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, , University of Toronto, ; Toronto, Ontario Canada M5S 3M2
                [2 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Chemistry, Faculty of Arts and Science, , University of Toronto, ; Toronto, Ontario Canada M5S 3H6
                [3 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Institute for Biomaterials and Biomedical Engineering, , University of Toronto, ; Toronto, Ontario Canada M5S 3G9
                [4 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Electrical and Computer Engineering, Faculty of Engineering, , University of Toronto, ; Toronto, Ontario Canada M5S 3G4
                [5 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Biochemistry, Faculty of Medicine, , University of Toronto, ; Toronto, Ontario Canada M5S 1A8
                Author information
                http://orcid.org/0000-0003-3360-5359
                Article
                298
                10.1038/s41467-017-00298-w
                5575008
                28851869
                aef176c6-7efa-4dec-9f23-30e2e35a375c
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 22 February 2017
                : 19 June 2017
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