On-chip light sheet illumination enables diagnostic size and concentration measurements of membrane vesicles in biofluidsElectronic supplementary information (ESI) available. See DOI: 10.1039/c3nr04432g
Cell-derived membrane vesicles that are released in biofluids, like blood or saliva, are emerging as potential non-invasive biomarkers for diseases, such as cancer. Techniques capable of measuring the size and concentration of membrane vesicles directly in biofluids are urgently needed. Fluorescence...
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creator | Deschout, Hendrik Raemdonck, Koen Stremersch, Stephan Maoddi, Pietro Mernier, Guillaume Renaud, Philippe Jiguet, Sébastien Hendrix, An Bracke, Marc Van den Broecke, Rudy Röding, Magnus Rudemo, Mats Demeester, Jo De Smedt, Stefaan C Strubbe, Filip Neyts, Kristiaan Braeckmans, Kevin |
description | Cell-derived membrane vesicles that are released in biofluids, like blood or saliva, are emerging as potential non-invasive biomarkers for diseases, such as cancer. Techniques capable of measuring the size and concentration of membrane vesicles directly in biofluids are urgently needed. Fluorescence single particle tracking microscopy has the potential of doing exactly that by labelling the membrane vesicles with a fluorescent label and analysing their Brownian motion in the biofluid. However, an unbound dye in the biofluid can cause high background intensity that strongly biases the fluorescence single particle tracking size and concentration measurements. While such background intensity can be avoided with light sheet illumination, current set-ups require specialty sample holders that are not compatible with high-throughput diagnostics. Here, a microfluidic chip with integrated light sheet illumination is reported, and accurate fluorescence single particle tracking size and concentration measurements of membrane vesicles in cell culture medium and in interstitial fluid collected from primary human breast tumours are demonstrated.
A microfluidic chip with integrated light sheet illumination allows accurate fluorescence single particle tracking size and concentration measurements of membrane vesicles in biofluids. |
doi_str_mv | 10.1039/c3nr04432g |
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See DOI: 10.1039/c3nr04432g</atitle><date>2014-01-16</date><risdate>2014</risdate><volume>6</volume><issue>3</issue><spage>1741</spage><epage>1747</epage><pages>1741-1747</pages><issn>2040-3364</issn><eissn>2040-3372</eissn><abstract>Cell-derived membrane vesicles that are released in biofluids, like blood or saliva, are emerging as potential non-invasive biomarkers for diseases, such as cancer. Techniques capable of measuring the size and concentration of membrane vesicles directly in biofluids are urgently needed. Fluorescence single particle tracking microscopy has the potential of doing exactly that by labelling the membrane vesicles with a fluorescent label and analysing their Brownian motion in the biofluid. However, an unbound dye in the biofluid can cause high background intensity that strongly biases the fluorescence single particle tracking size and concentration measurements. While such background intensity can be avoided with light sheet illumination, current set-ups require specialty sample holders that are not compatible with high-throughput diagnostics. Here, a microfluidic chip with integrated light sheet illumination is reported, and accurate fluorescence single particle tracking size and concentration measurements of membrane vesicles in cell culture medium and in interstitial fluid collected from primary human breast tumours are demonstrated.
A microfluidic chip with integrated light sheet illumination allows accurate fluorescence single particle tracking size and concentration measurements of membrane vesicles in biofluids.</abstract><doi>10.1039/c3nr04432g</doi><tpages>7</tpages></addata></record> |
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title | On-chip light sheet illumination enables diagnostic size and concentration measurements of membrane vesicles in biofluidsElectronic supplementary information (ESI) available. See DOI: 10.1039/c3nr04432g |
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