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      Bio-inspired detoxification using 3D-printed hydrogel nanocomposites

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          Abstract

          Rationally designed nanoparticles that can bind toxins show great promise for detoxification. However, the conventional intravenous administration of nanoparticles for detoxification often leads to nanoparticle accumulation in the liver, posing a risk of secondary poisoning especially in liver-failure patients. Here we present a liver-inspired three-dimensional (3D) detoxification device. This device is created by 3D printing of designer hydrogels with functional polydiacetylene nanoparticles installed in the hydrogel matrix. The nanoparticles can attract, capture and sense toxins, while the 3D matrix with a modified liver lobule microstructure allows toxins to be trapped efficiently. Our results show that the toxin solution completely loses its virulence after treatment using this biomimetic detoxification device. This work provides a proof-of-concept of detoxification by a 3D-printed biomimetic nanocomposite construct in hydrogel, and could lead to the development of alternative detoxification platforms.

          Abstract

          Nanoparticles capable of selectively binding target chemicals have potential for detoxification processes, but can lead to accumulation in the liver. Here the authors show a 3D-printed device containing functional nanoparticles, allowing the detox potential to be realised while holding the particles in place.

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          Most cited references33

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          Designing cell-compatible hydrogels for biomedical applications.

          Hydrogels are polymeric materials distinguished by high water content and diverse physical properties. They can be engineered to resemble the extracellular environment of the body's tissues in ways that enable their use in medical implants, biosensors, and drug-delivery devices. Cell-compatible hydrogels are designed by using a strategy of coordinated control over physical properties and bioactivity to influence specific interactions with cellular systems, including spatial and temporal patterns of biochemical and biomechanical cues known to modulate cell behavior. Important new discoveries in stem cell research, cancer biology, and cellular morphogenesis have been realized with model hydrogel systems premised on these designs. Basic and clinical applications for hydrogels in cell therapy, tissue engineering, and biomedical research continue to drive design improvements using performance-based materials engineering paradigms.
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            Liver regeneration: from myth to mechanism.

            The unusual regenerative properties of the liver are a logical adaptation by organisms, as the liver is the main detoxifying organ of the body and is likely to be injured by ingested toxins. The numerous cytokine- and growth-factor-mediated pathways that are involved in regulating liver regeneration are being successfully dissected using molecular and genetic approaches. So what is known about this process at present and which questions remain?
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              A tissue-like printed material.

              Living cells communicate and cooperate to produce the emergent properties of tissues. Synthetic mimics of cells, such as liposomes, are typically incapable of cooperation and therefore cannot readily display sophisticated collective behavior. We printed tens of thousands of picoliter aqueous droplets that become joined by single lipid bilayers to form a cohesive material with cooperating compartments. Three-dimensional structures can be built with heterologous droplets in software-defined arrangements. The droplet networks can be functionalized with membrane proteins; for example, to allow rapid electrical communication along a specific path. The networks can also be programmed by osmolarity gradients to fold into otherwise unattainable designed structures. Printed droplet networks might be interfaced with tissues, used as tissue engineering substrates, or developed as mimics of living tissue.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                08 May 2014
                : 5
                : 3774
                Affiliations
                [1 ]State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University , Chengdu 610041, P.R. China
                [2 ]Shiley Eye Center and Institute for Genomic Medicine, University of California , San Diego, La Jolla, California 92093, USA
                [3 ]Department of NanoEngineering, University of California , San Diego, La Jolla, California 92093, USA
                [4 ]School of Chemistry and Chemical Engineering, Shaanxi Normal University , Xi'an 710062, P.R. China
                [5 ]Biomaterials and Tissue Engineering Center, University of California , San Diego, La Jolla, California 92093, USA
                [6 ]Veterans Administration Healthcare System , San Diego, California 92093, USA
                [7 ]These authors contributed equally to this work and are co-first authors
                Author notes
                Article
                ncomms4774
                10.1038/ncomms4774
                4024742
                24805923
                eeecdec1-8f83-41c2-ae1e-47498196f442
                Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

                History
                : 06 November 2013
                : 02 April 2014
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