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      Long-range optofluidic control with plasmon heating

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          Abstract

          Using light to manipulate fluids has been a long-sought-after goal for lab-on-a-chip applications to address the size mismatch between bulky external fluid controllers and microfluidic devices. Yet, this goal has remained elusive due to the complexity of thermally driven fluid dynamic phenomena, and the lack of approaches that allow comprehensive multiscale and multiparameter studies. Here, we report an innovative optofluidic platform that fulfills this need by combining digital holographic microscopy with state-of-the-art thermoplasmonics, allowing us to identify the different contributions from thermophoresis, thermo-osmosis, convection, and radiation pressure. In our experiments, we demonstrate that a local thermal perturbation at the microscale can lead to mm-scale changes in both the particle and fluid dynamics, thus achieving long-range transport. Furthermore, thanks to a comprehensive parameter study involving sample geometry, temperature increase, light fluence, and size of the heat source, we showcase an integrated and reconfigurable all-optical control strategy for microfluidic devices, thereby opening new frontiers in fluid actuation technology.

          Abstract

          Here, the authors combine digital holographic microscopy with thermoplasmonics in order to identify different contributions of thermally driven fluid dynamic phenomena. They find that local thermal perturbation leads to long-range changes in the dynamics of the system, and demonstrate an all-optical control strategy for microfluidic devices.

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          In situ click chemistry generation of cyclooxygenase-2 inhibitors

          Cyclooxygenase-2 isozyme is a promising anti-inflammatory drug target, and overexpression of this enzyme is also associated with several cancers and neurodegenerative diseases. The amino-acid sequence and structural similarity between inducible cyclooxygenase-2 and housekeeping cyclooxygenase-1 isoforms present a significant challenge to design selective cyclooxygenase-2 inhibitors. Herein, we describe the use of the cyclooxygenase-2 active site as a reaction vessel for the in situ generation of its own highly specific inhibitors. Multi-component competitive-binding studies confirmed that the cyclooxygenase-2 isozyme can judiciously select most appropriate chemical building blocks from a pool of chemicals to build its own highly potent inhibitor. Herein, with the use of kinetic target-guided synthesis, also termed as in situ click chemistry, we describe the discovery of two highly potent and selective cyclooxygenase-2 isozyme inhibitors. The in vivo anti-inflammatory activity of these two novel small molecules is significantly higher than that of widely used selective cyclooxygenase-2 inhibitors.
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            Microfluidics: Fluid physics at the nanoliter scale

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              Preparation and Growth Mechanism of Gold Nanorods (NRs) Using Seed-Mediated Growth Method

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                Author and article information

                Contributors
                jarroyo@ethz.ch
                rquidant@ethz.ch
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                31 March 2021
                31 March 2021
                2021
                : 12
                : 2001
                Affiliations
                [1 ]ICFO – Institut de Ciències Fotòniques, The Barcelona Institute of Science and Technology, Castelldefels (Barcelona), Spain
                [2 ]GRID grid.5801.c, ISNI 0000 0001 2156 2780, Nanophotonic Systems Laboratory, Department of Mechanical and Process Engineering, ETH Zurich, ; Zurich, Switzerland
                [3 ]GRID grid.425902.8, ISNI 0000 0000 9601 989X, Institució Catalana de Recerca i Estudis Avançats (ICREA), ; Barcelona, Spain
                Author information
                https://orcid.org/http://orcid.org/0000-0002-7191-8594
                https://orcid.org/http://orcid.org/0000-0003-4574-4356
                https://orcid.org/http://orcid.org/0000-0002-0657-051X
                https://orcid.org/http://orcid.org/0000-0001-8995-8976
                Article
                22280
                10.1038/s41467-021-22280-3
                8012589
                33790293
                67f57091-18e3-4a94-8899-d3921095b6e3
                © The Author(s) 2021

                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
                : 4 June 2020
                : 23 February 2021
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                nanophotonics and plasmonics,optics and photonics,optofluidics
                Uncategorized
                nanophotonics and plasmonics, optics and photonics, optofluidics

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