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      Reaction injection molding of hydrophilic-in-hydrophobic femtolitre-well arrays

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          Abstract

          Patterning of micro- and nanoscale topologies and surface properties of polymer devices is of particular importance for a broad range of life science applications, including cell-adhesion assays and highly sensitive bioassays. The manufacturing of such devices necessitates cumbersome multiple-step fabrication procedures and results in surface properties which degrade over time. This critically hinders their wide-spread dissemination. Here, we simultaneously mold and surface energy pattern microstructures in off-stoichiometric thiol-ene by area-selective monomer self-assembly in a rapid micro-reaction injection molding cycle. We replicated arrays of 1,843,650 hydrophilic-in-hydrophobic femtolitre-wells with long-term stable surface properties and magnetically trapped beads with 75% and 87.2% efficiency in single- and multiple-seeding events, respectively. These results form the basis for ultrasensitive digital biosensors, specifically, and for the fabrication of medical devices and life science research tools, generally.

          Simultaneous microstructuring and surface modification of microfluidic bioreactors

          Researchers from Sweden and Belgium have developed a simplified technique to create microfluidic devices with patterns of modified surface properties. Microfluidic devices, such as the one demonstrated here by a team led by Wouter van der Wijngaart, from KTH Royal Institute of Technology, Sweden, utilize polymer microstructures with hydrophobic and hydrophilic properties to manipulate fluids on a tiny scale. This enables ‘lab-on-a-chip’ experiments with a diverse array of applications. However, current devices suffer from complicated fabrication processes and a limited lifespan. van der Wijngaart and his team used the polymer ‘off-stoichiometric thiol-ene’ to merge a rapid replication technique called reaction injection molding with a method to self-assemble hydrophobic and hydrophilic micropatterns in a single, rapid fabrication step. The researchers hope that their results will form the basis for future microfluidic chip manufacturing and lead to the creation of ultrasensitive life science research tools.

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          Most cited references25

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          Thiol-ene click chemistry.

          Following Sharpless' visionary characterization of several idealized reactions as click reactions, the materials science and synthetic chemistry communities have pursued numerous routes toward the identification and implementation of these click reactions. Herein, we review the radical-mediated thiol-ene reaction as one such click reaction. This reaction has all the desirable features of a click reaction, being highly efficient, simple to execute with no side products and proceeding rapidly to high yield. Further, the thiol-ene reaction is most frequently photoinitiated, particularly for photopolymerizations resulting in highly uniform polymer networks, promoting unique capabilities related to spatial and temporal control of the click reaction. The reaction mechanism and its implementation in various synthetic methodologies, biofunctionalization, surface and polymer modification, and polymerization are all reviewed.
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            Thiol-enes: Chemistry of the past with promise for the future

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              Polymer microfabrication technologies for microfluidic systems.

              Polymers have assumed the leading role as substrate materials for microfluidic devices in recent years. They offer a broad range of material parameters as well as material and surface chemical properties which enable microscopic design features that cannot be realised by any other class of materials. A similar range of fabrication technologies exist to generate microfluidic devices from these materials. This review will introduce the currently relevant microfabrication technologies such as replication methods like hot embossing, injection molding, microthermoforming and casting as well as photodefining methods like lithography and laser ablation for microfluidic systems and discuss academic and industrial considerations for their use. A section on back-end processing completes the overview.
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                Author and article information

                Contributors
                rezazs@kth.se
                wouter@kth.se
                Journal
                Microsyst Nanoeng
                Microsyst Nanoeng
                Microsystems & Nanoengineering
                Nature Publishing Group UK (London )
                2096-1030
                2055-7434
                3 June 2019
                3 June 2019
                2019
                : 5
                : 25
                Affiliations
                [1 ]ISNI 0000000121581746, GRID grid.5037.1, Department of Micro- and Nanosystems, , KTH Royal Institute of Technology, ; Stockholm, Sweden
                [2 ]ISNI 0000 0001 0668 7884, GRID grid.5596.f, Department of Biosystems, , KU Leuven, ; Willem de Croylaan 42, 3001 Leuven, Belgium
                Author information
                http://orcid.org/0000-0003-4322-6192
                http://orcid.org/0000-0001-5906-0532
                http://orcid.org/0000-0002-7240-8377
                http://orcid.org/0000-0002-4115-4677
                http://orcid.org/0000-0001-9177-1174
                http://orcid.org/0000-0001-8143-6794
                http://orcid.org/0000-0001-8248-6670
                Article
                65
                10.1038/s41378-019-0065-2
                6545322
                da8ff3c1-cc33-477c-bed3-caeba977f70d
                © The Author(s) 2019

                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
                : 6 November 2018
                : 16 February 2019
                : 13 March 2019
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                Custom metadata
                © The Author(s) 2019

                nanoscale devices,nanoscale materials
                nanoscale devices, nanoscale materials

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