Polyshrink™ based microfluidic chips and protein microarrays
Autor: | Céline A. Mandon, Christophe A. Marquette, Loïc J. Blum, Kevin A. Heyries |
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Přispěvatelé: | Institut de Chimie et Biochimie Moléculaires et Supramoléculaires (ICBMS), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Institut de Chimie du CNRS (INC)-École Supérieure Chimie Physique Électronique de Lyon-Centre National de la Recherche Scientifique (CNRS) |
Rok vydání: | 2010 |
Předmět: |
MESH: Microelectrodes
02 engineering and technology 01 natural sciences MESH: Antibodies Monoclonal chemistry.chemical_compound MESH: Ink Electrochemistry MESH: Animals MESH: Proteins Biochip Immunoassay Spots MESH: Protein Array Analysis Antibodies Monoclonal MESH: Polystyrenes Serum Albumin Bovine Equipment Design General Medicine Microfluidic Analytical Techniques 021001 nanoscience & nanotechnology MESH: Cattle Biochip Cell adhesion Protein microarray Microfluidic Serology MESH: Microfluidic Analytical Techniques Protein microarray Printing Ink 0210 nano-technology MESH: Immunoassay Biotechnology Materials science MESH: Chemiluminescent Measurements Microfluidics Protein Array Analysis Biomedical Engineering Biophysics Nanotechnology Miniaturization Animals Humans MESH: Printing [SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biochemistry [q-bio.BM] MESH: Humans Inkwell 010401 analytical chemistry Proteins 0104 chemical sciences MESH: Hela Cells chemistry Luminescent Measurements Polystyrenes Cattle Polystyrene Microelectrodes MESH: Serum Albumin Bovine HeLa Cells MESH: Equipment Design |
Zdroj: | Biosensors and Bioelectronics Biosensors and Bioelectronics, Elsevier, 2010, 26 (4), pp.1218-24. ⟨10.1016/j.bios.2010.05.028⟩ |
ISSN: | 0956-5663 |
DOI: | 10.1016/j.bios.2010.05.028 |
Popis: | International audience; A new approach for the rapid production of microfluidic chips integrating protein spots is described. The technology, called "Print-n-Shrink", is based on the screen-printing of a microfluidic design (using a dielectric ink) onto Polyshrink™ polystyrene sheets. The initial printing which have a minimum size of 15 μm (height)×230 μm (width) was thermally treated (30s, 163°C) to shrink and generate features of 85 μm (height)×100 μm (width). Protein spots were also demonstrated to be shrinkable and arrays of 50 μm-size spots with density up to 6400 spots/cm(2) were achieved. Proteins such as monoclonal antibodies or cellular adhesion proteins were thus spotted onto the Polyshrink™ sheets and shrunk together with the microfluidic design, creating complete biochips integrating both complex microfluidic designs and protein spots for bioanalytical applications. These shrunk spots were shown to host enough active proteins to enable the achievement of both sensitive sandwich immunoassays (Brain Natriuretic Peptide, C-Reactive Protein and c-Troponin I) and localized cell culture. |
Databáze: | OpenAIRE |
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