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A surface plasmon resonance imaging system for the stimulated living cell analysis
In this paper, a surface plasmon resonance imaging(SPRI) system for cell analysis is developed for obtaining the surface plasmon resonance(SPR) signal from the interactions between cells and different stimuli. The system is constructed with a red laser light source, a P-polarizer, a glass prism, a 5...
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Published in: | Optoelectronics letters 2015, Vol.11 (1), p.77-80 |
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creator | 张璐璐 陈兴 杜洋 张倩 李辉 孙建海 崔大付 |
description | In this paper, a surface plasmon resonance imaging(SPRI) system for cell analysis is developed for obtaining the surface plasmon resonance(SPR) signal from the interactions between cells and different stimuli. The system is constructed with a red laser light source, a P-polarizer, a glass prism, a 5× objective lens, a charge coupled device(CCD) camera, a gold sensor chip, a polydimethylsiloxane(PDMS) reaction well and a mechanical scanning device. The system is applied to mapping living cells in response to stimuli by characterization of the refractive index(RI) changes. Cell responses to K+ in KCl solutions with concentrations of 5 mmol/L, 20 mmol/L, 50 mmol/L and 100 mmol/L are collected, which indicates that the SPRI method can distinguish the concentration of the stimuli. Furthermore, cell responses to epidermal growth factor(EGF) and vascular endothelial growth factor(VEGF) are studied independently. The binding of EGF receptor(EGFR) and EGF is collected as the first signal, and the internal change in cells is recorded as the second signal. The cell response to VEGF is different from that to EGF, which indicates that the SPRI as a label-free, real-time, fast and quantitative method has a potential to distinguish the cell responses to different stimuli. |
doi_str_mv | 10.1007/s11801-015-4171-6 |
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The cell response to VEGF is different from that to EGF, which indicates that the SPRI as a label-free, real-time, fast and quantitative method has a potential to distinguish the cell responses to different stimuli.</description><identifier>ISSN: 1673-1905</identifier><identifier>EISSN: 1993-5013</identifier><identifier>DOI: 10.1007/s11801-015-4171-6</identifier><language>eng</language><publisher>Heidelberg: Tianjin University of Technology</publisher><subject>Lasers ; Optical Devices ; Optics ; Photonics ; Physics ; Physics and Astronomy ; VEGF ; 成像系统 ; 激活 ; 细胞分析 ; 聚二甲基硅氧烷 ; 血管内皮生长因子 ; 表皮生长因子受体 ; 表面等离子体共振</subject><ispartof>Optoelectronics letters, 2015, Vol.11 (1), p.77-80</ispartof><rights>Tianjin University of Technology and Springer-Verlag Berlin Heidelberg 2015</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-a0b7ace6675d2a12a5a079e1a64582b6c3a01d19ec86ffdd111220066f2030493</citedby><cites>FETCH-LOGICAL-c315t-a0b7ace6675d2a12a5a079e1a64582b6c3a01d19ec86ffdd111220066f2030493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/88368X/88368X.jpg</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids></links><search><creatorcontrib>张璐璐 陈兴 杜洋 张倩 李辉 孙建海 崔大付</creatorcontrib><title>A surface plasmon resonance imaging system for the stimulated living cell analysis</title><title>Optoelectronics letters</title><addtitle>Optoelectron. Lett</addtitle><addtitle>Opto-electronics Letters</addtitle><description>In this paper, a surface plasmon resonance imaging(SPRI) system for cell analysis is developed for obtaining the surface plasmon resonance(SPR) signal from the interactions between cells and different stimuli. The system is constructed with a red laser light source, a P-polarizer, a glass prism, a 5× objective lens, a charge coupled device(CCD) camera, a gold sensor chip, a polydimethylsiloxane(PDMS) reaction well and a mechanical scanning device. The system is applied to mapping living cells in response to stimuli by characterization of the refractive index(RI) changes. Cell responses to K+ in KCl solutions with concentrations of 5 mmol/L, 20 mmol/L, 50 mmol/L and 100 mmol/L are collected, which indicates that the SPRI method can distinguish the concentration of the stimuli. Furthermore, cell responses to epidermal growth factor(EGF) and vascular endothelial growth factor(VEGF) are studied independently. The binding of EGF receptor(EGFR) and EGF is collected as the first signal, and the internal change in cells is recorded as the second signal. The cell response to VEGF is different from that to EGF, which indicates that the SPRI as a label-free, real-time, fast and quantitative method has a potential to distinguish the cell responses to different stimuli.</description><subject>Lasers</subject><subject>Optical Devices</subject><subject>Optics</subject><subject>Photonics</subject><subject>Physics</subject><subject>Physics and Astronomy</subject><subject>VEGF</subject><subject>成像系统</subject><subject>激活</subject><subject>细胞分析</subject><subject>聚二甲基硅氧烷</subject><subject>血管内皮生长因子</subject><subject>表皮生长因子受体</subject><subject>表面等离子体共振</subject><issn>1673-1905</issn><issn>1993-5013</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoWLQ_wFvwHp1JNsnusRS_oCCInkO6m91u2Y-a2Qr996a0eHQuMwzzzPvyMnaH8IAA9pEQc0ABqEWGFoW5YDMsCiU0oLpMs7FKYAH6ms2JtpBKSZtnxYx9LDjtY-3LwHedp34ceAw0Dn5Im7b3TTs0nA40hZ7XY-TTJnCa2n7f-SlUvGt_jgdl6DruB98dqKVbdlX7jsL83G_Y1_PT5_JVrN5f3paLlSgV6kl4WNska4zVlfQovfZgi4DeZDqXa1MqD1hhEcrc1HVVIaKUAMbUEhRkhbphePpbxpEohtrtYnIcDw7BHXNxp1xcysUdc3EmMfLEULodmhDddtzHZJz-he7PQptxaL4T96dkjNLaGJmrX0C9cRM</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>张璐璐 陈兴 杜洋 张倩 李辉 孙建海 崔大付</creator><general>Tianjin University of Technology</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W92</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2015</creationdate><title>A surface plasmon resonance imaging system for the stimulated living cell analysis</title><author>张璐璐 陈兴 杜洋 张倩 李辉 孙建海 崔大付</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-a0b7ace6675d2a12a5a079e1a64582b6c3a01d19ec86ffdd111220066f2030493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Lasers</topic><topic>Optical Devices</topic><topic>Optics</topic><topic>Photonics</topic><topic>Physics</topic><topic>Physics and Astronomy</topic><topic>VEGF</topic><topic>成像系统</topic><topic>激活</topic><topic>细胞分析</topic><topic>聚二甲基硅氧烷</topic><topic>血管内皮生长因子</topic><topic>表皮生长因子受体</topic><topic>表面等离子体共振</topic><toplevel>online_resources</toplevel><creatorcontrib>张璐璐 陈兴 杜洋 张倩 李辉 孙建海 崔大付</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>中文科技期刊数据库-工程技术</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><jtitle>Optoelectronics letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>张璐璐 陈兴 杜洋 张倩 李辉 孙建海 崔大付</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A surface plasmon resonance imaging system for the stimulated living cell analysis</atitle><jtitle>Optoelectronics letters</jtitle><stitle>Optoelectron. Lett</stitle><addtitle>Opto-electronics Letters</addtitle><date>2015</date><risdate>2015</risdate><volume>11</volume><issue>1</issue><spage>77</spage><epage>80</epage><pages>77-80</pages><issn>1673-1905</issn><eissn>1993-5013</eissn><abstract>In this paper, a surface plasmon resonance imaging(SPRI) system for cell analysis is developed for obtaining the surface plasmon resonance(SPR) signal from the interactions between cells and different stimuli. The system is constructed with a red laser light source, a P-polarizer, a glass prism, a 5× objective lens, a charge coupled device(CCD) camera, a gold sensor chip, a polydimethylsiloxane(PDMS) reaction well and a mechanical scanning device. The system is applied to mapping living cells in response to stimuli by characterization of the refractive index(RI) changes. Cell responses to K+ in KCl solutions with concentrations of 5 mmol/L, 20 mmol/L, 50 mmol/L and 100 mmol/L are collected, which indicates that the SPRI method can distinguish the concentration of the stimuli. Furthermore, cell responses to epidermal growth factor(EGF) and vascular endothelial growth factor(VEGF) are studied independently. The binding of EGF receptor(EGFR) and EGF is collected as the first signal, and the internal change in cells is recorded as the second signal. The cell response to VEGF is different from that to EGF, which indicates that the SPRI as a label-free, real-time, fast and quantitative method has a potential to distinguish the cell responses to different stimuli.</abstract><cop>Heidelberg</cop><pub>Tianjin University of Technology</pub><doi>10.1007/s11801-015-4171-6</doi><tpages>4</tpages></addata></record> |
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subjects | Lasers Optical Devices Optics Photonics Physics Physics and Astronomy VEGF 成像系统 激活 细胞分析 聚二甲基硅氧烷 血管内皮生长因子 表皮生长因子受体 表面等离子体共振 |
title | A surface plasmon resonance imaging system for the stimulated living cell analysis |
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