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      Cyclic olefin polymers: emerging materials for lab-on-a-chip applications

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          Microfluidic devices fabricated in poly(dimethylsiloxane) for biological studies.

          This review describes microfluidic systems in poly(dimethylsiloxane) (PDMS) for biological studies. Properties of PDMS that make it a suitable platform for miniaturized biological studies, techniques for fabricating PDMS microstructures, and methods for controlling fluid flow in microchannels are discussed. Biological procedures that have been miniaturized into PDMS-based microdevices include immunoassays, separation of proteins and DNA, sorting and manipulation of cells, studies of cells in microchannels exposed to laminar flows of fluids, and large-scale, combinatorial screening. The review emphasizes the advantages of miniaturization for biological analysis, such as efficiency of the device and special insights into cell biology.
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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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              Bonding of thermoplastic polymer microfluidics

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                Author and article information

                Journal
                Microfluidics and Nanofluidics
                Microfluid Nanofluid
                Springer Nature
                1613-4982
                1613-4990
                August 2010
                April 2010
                : 9
                : 2-3
                : 145-161
                Article
                10.1007/s10404-010-0605-4
                efdb91ab-1e64-40f9-9612-f859f29d88c3
                © 2010
                History

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