Optical forces for noninvasive cellular analysis

A novel, noninvasive measurement technique for quantitative cellular analysis is presented that utilizes the forces generated by an optical beam to evaluate the physical properties of live cells in suspension. In this analysis, a focused, near-infrared laser line with a high cross-sectional intensit...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied Optics 2003-10, Vol.42 (28), p.5765-5773
Hauptverfasser: Wang, Mark M, Schnabel, Catherine A, Chachisvilis, Mirianas, Yang, Rong, Paliotti, Michael J, Simons, Laura A, McMullin, Laura, Hagen, Norbert, Lykstad, Kristie, Tu, Eugene, Pestana, Luis M, Sur, Sudipto, Zhang, Haichuan, Butler, William F, Kariv, Ilona, Marchand, Philippe J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 5773
container_issue 28
container_start_page 5765
container_title Applied Optics
container_volume 42
creator Wang, Mark M
Schnabel, Catherine A
Chachisvilis, Mirianas
Yang, Rong
Paliotti, Michael J
Simons, Laura A
McMullin, Laura
Hagen, Norbert
Lykstad, Kristie
Tu, Eugene
Pestana, Luis M
Sur, Sudipto
Zhang, Haichuan
Butler, William F
Kariv, Ilona
Marchand, Philippe J
description A novel, noninvasive measurement technique for quantitative cellular analysis is presented that utilizes the forces generated by an optical beam to evaluate the physical properties of live cells in suspension. In this analysis, a focused, near-infrared laser line with a high cross-sectional intensity gradient is rapidly scanned across a field of cells, and the interaction of those cells with the beam is monitored. The response of each cell to the laser depends on its size, structure, morphology, composition, and surface membrane properties; therefore, with this technique, cell populations of different type, treatment, or biological state can be compared. To demonstrate the utility of this cell analysis platform, we evaluated the early stages of apoptosis induced in the U937 cancer cell line by the drug camptothecin and compared the results with established reference assays. Measurements on our platform show detection of cellular changes earlier than either of the fluorescence-based Annexin V or caspase assays. Because no labeling or additional cell processing is required and because accurate assays can be performed with a small number of cells, this measurement technique may find suitable applications in cell research, medical diagnostics, and drug discovery.
doi_str_mv 10.1364/AO.42.005765
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75743500</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>75743500</sourcerecordid><originalsourceid>FETCH-LOGICAL-c287t-3c062a1acb592b42d9d8deac806186fdd8c692c2ba1aa976f8eedad62de234d3</originalsourceid><addsrcrecordid>eNpFkDtrwzAUhUVpadK0W-fiqVOdSlcPS2MIfUHAS4Zu4lqSwcWxUykO5N_XJoFO5w4fh3M_Qh4ZXTKuxOuqXApYUioLJa_InEluciEBrqdbmpyB_p6Ru5R-KOVSmOKWzNgIaCPYnNByf2gctlndRxfSFFnXd013xNQcQ-ZC2w4txgw7bE-pSffkpsY2hYdLLsj2_W27_sw35cfXerXJHejikHNHFSBDV0kDlQBvvPYBnaaKaVV7r50y4KAaGTSFqnUIHr0CH4ALzxfk-Vy7j_3vENLB7po0jcEu9EOyhSwEl-NHC_JyBl3sU4qhtvvY7DCeLKN2EmRXpRVgz4JG_OnSO1S74P_hixH-B5LoYRY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75743500</pqid></control><display><type>article</type><title>Optical forces for noninvasive cellular analysis</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><source>Optica Publishing Group Journals</source><creator>Wang, Mark M ; Schnabel, Catherine A ; Chachisvilis, Mirianas ; Yang, Rong ; Paliotti, Michael J ; Simons, Laura A ; McMullin, Laura ; Hagen, Norbert ; Lykstad, Kristie ; Tu, Eugene ; Pestana, Luis M ; Sur, Sudipto ; Zhang, Haichuan ; Butler, William F ; Kariv, Ilona ; Marchand, Philippe J</creator><creatorcontrib>Wang, Mark M ; Schnabel, Catherine A ; Chachisvilis, Mirianas ; Yang, Rong ; Paliotti, Michael J ; Simons, Laura A ; McMullin, Laura ; Hagen, Norbert ; Lykstad, Kristie ; Tu, Eugene ; Pestana, Luis M ; Sur, Sudipto ; Zhang, Haichuan ; Butler, William F ; Kariv, Ilona ; Marchand, Philippe J</creatorcontrib><description>A novel, noninvasive measurement technique for quantitative cellular analysis is presented that utilizes the forces generated by an optical beam to evaluate the physical properties of live cells in suspension. In this analysis, a focused, near-infrared laser line with a high cross-sectional intensity gradient is rapidly scanned across a field of cells, and the interaction of those cells with the beam is monitored. The response of each cell to the laser depends on its size, structure, morphology, composition, and surface membrane properties; therefore, with this technique, cell populations of different type, treatment, or biological state can be compared. To demonstrate the utility of this cell analysis platform, we evaluated the early stages of apoptosis induced in the U937 cancer cell line by the drug camptothecin and compared the results with established reference assays. Measurements on our platform show detection of cellular changes earlier than either of the fluorescence-based Annexin V or caspase assays. Because no labeling or additional cell processing is required and because accurate assays can be performed with a small number of cells, this measurement technique may find suitable applications in cell research, medical diagnostics, and drug discovery.</description><identifier>ISSN: 1559-128X</identifier><identifier>ISSN: 0003-6935</identifier><identifier>EISSN: 1539-4522</identifier><identifier>DOI: 10.1364/AO.42.005765</identifier><identifier>PMID: 14528941</identifier><language>eng</language><publisher>United States</publisher><subject>Apoptosis ; Humans ; Lasers ; Neoplasms - pathology ; Neoplasms - physiopathology ; Optics and Photonics - instrumentation ; Time Factors ; Tumor Cells, Cultured</subject><ispartof>Applied Optics, 2003-10, Vol.42 (28), p.5765-5773</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c287t-3c062a1acb592b42d9d8deac806186fdd8c692c2ba1aa976f8eedad62de234d3</citedby><cites>FETCH-LOGICAL-c287t-3c062a1acb592b42d9d8deac806186fdd8c692c2ba1aa976f8eedad62de234d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14528941$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Mark M</creatorcontrib><creatorcontrib>Schnabel, Catherine A</creatorcontrib><creatorcontrib>Chachisvilis, Mirianas</creatorcontrib><creatorcontrib>Yang, Rong</creatorcontrib><creatorcontrib>Paliotti, Michael J</creatorcontrib><creatorcontrib>Simons, Laura A</creatorcontrib><creatorcontrib>McMullin, Laura</creatorcontrib><creatorcontrib>Hagen, Norbert</creatorcontrib><creatorcontrib>Lykstad, Kristie</creatorcontrib><creatorcontrib>Tu, Eugene</creatorcontrib><creatorcontrib>Pestana, Luis M</creatorcontrib><creatorcontrib>Sur, Sudipto</creatorcontrib><creatorcontrib>Zhang, Haichuan</creatorcontrib><creatorcontrib>Butler, William F</creatorcontrib><creatorcontrib>Kariv, Ilona</creatorcontrib><creatorcontrib>Marchand, Philippe J</creatorcontrib><title>Optical forces for noninvasive cellular analysis</title><title>Applied Optics</title><addtitle>Appl Opt</addtitle><description>A novel, noninvasive measurement technique for quantitative cellular analysis is presented that utilizes the forces generated by an optical beam to evaluate the physical properties of live cells in suspension. In this analysis, a focused, near-infrared laser line with a high cross-sectional intensity gradient is rapidly scanned across a field of cells, and the interaction of those cells with the beam is monitored. The response of each cell to the laser depends on its size, structure, morphology, composition, and surface membrane properties; therefore, with this technique, cell populations of different type, treatment, or biological state can be compared. To demonstrate the utility of this cell analysis platform, we evaluated the early stages of apoptosis induced in the U937 cancer cell line by the drug camptothecin and compared the results with established reference assays. Measurements on our platform show detection of cellular changes earlier than either of the fluorescence-based Annexin V or caspase assays. Because no labeling or additional cell processing is required and because accurate assays can be performed with a small number of cells, this measurement technique may find suitable applications in cell research, medical diagnostics, and drug discovery.</description><subject>Apoptosis</subject><subject>Humans</subject><subject>Lasers</subject><subject>Neoplasms - pathology</subject><subject>Neoplasms - physiopathology</subject><subject>Optics and Photonics - instrumentation</subject><subject>Time Factors</subject><subject>Tumor Cells, Cultured</subject><issn>1559-128X</issn><issn>0003-6935</issn><issn>1539-4522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkDtrwzAUhUVpadK0W-fiqVOdSlcPS2MIfUHAS4Zu4lqSwcWxUykO5N_XJoFO5w4fh3M_Qh4ZXTKuxOuqXApYUioLJa_InEluciEBrqdbmpyB_p6Ru5R-KOVSmOKWzNgIaCPYnNByf2gctlndRxfSFFnXd013xNQcQ-ZC2w4txgw7bE-pSffkpsY2hYdLLsj2_W27_sw35cfXerXJHejikHNHFSBDV0kDlQBvvPYBnaaKaVV7r50y4KAaGTSFqnUIHr0CH4ALzxfk-Vy7j_3vENLB7po0jcEu9EOyhSwEl-NHC_JyBl3sU4qhtvvY7DCeLKN2EmRXpRVgz4JG_OnSO1S74P_hixH-B5LoYRY</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>Wang, Mark M</creator><creator>Schnabel, Catherine A</creator><creator>Chachisvilis, Mirianas</creator><creator>Yang, Rong</creator><creator>Paliotti, Michael J</creator><creator>Simons, Laura A</creator><creator>McMullin, Laura</creator><creator>Hagen, Norbert</creator><creator>Lykstad, Kristie</creator><creator>Tu, Eugene</creator><creator>Pestana, Luis M</creator><creator>Sur, Sudipto</creator><creator>Zhang, Haichuan</creator><creator>Butler, William F</creator><creator>Kariv, Ilona</creator><creator>Marchand, Philippe J</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20031001</creationdate><title>Optical forces for noninvasive cellular analysis</title><author>Wang, Mark M ; Schnabel, Catherine A ; Chachisvilis, Mirianas ; Yang, Rong ; Paliotti, Michael J ; Simons, Laura A ; McMullin, Laura ; Hagen, Norbert ; Lykstad, Kristie ; Tu, Eugene ; Pestana, Luis M ; Sur, Sudipto ; Zhang, Haichuan ; Butler, William F ; Kariv, Ilona ; Marchand, Philippe J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c287t-3c062a1acb592b42d9d8deac806186fdd8c692c2ba1aa976f8eedad62de234d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Apoptosis</topic><topic>Humans</topic><topic>Lasers</topic><topic>Neoplasms - pathology</topic><topic>Neoplasms - physiopathology</topic><topic>Optics and Photonics - instrumentation</topic><topic>Time Factors</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Mark M</creatorcontrib><creatorcontrib>Schnabel, Catherine A</creatorcontrib><creatorcontrib>Chachisvilis, Mirianas</creatorcontrib><creatorcontrib>Yang, Rong</creatorcontrib><creatorcontrib>Paliotti, Michael J</creatorcontrib><creatorcontrib>Simons, Laura A</creatorcontrib><creatorcontrib>McMullin, Laura</creatorcontrib><creatorcontrib>Hagen, Norbert</creatorcontrib><creatorcontrib>Lykstad, Kristie</creatorcontrib><creatorcontrib>Tu, Eugene</creatorcontrib><creatorcontrib>Pestana, Luis M</creatorcontrib><creatorcontrib>Sur, Sudipto</creatorcontrib><creatorcontrib>Zhang, Haichuan</creatorcontrib><creatorcontrib>Butler, William F</creatorcontrib><creatorcontrib>Kariv, Ilona</creatorcontrib><creatorcontrib>Marchand, Philippe J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Applied Optics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Mark M</au><au>Schnabel, Catherine A</au><au>Chachisvilis, Mirianas</au><au>Yang, Rong</au><au>Paliotti, Michael J</au><au>Simons, Laura A</au><au>McMullin, Laura</au><au>Hagen, Norbert</au><au>Lykstad, Kristie</au><au>Tu, Eugene</au><au>Pestana, Luis M</au><au>Sur, Sudipto</au><au>Zhang, Haichuan</au><au>Butler, William F</au><au>Kariv, Ilona</au><au>Marchand, Philippe J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optical forces for noninvasive cellular analysis</atitle><jtitle>Applied Optics</jtitle><addtitle>Appl Opt</addtitle><date>2003-10-01</date><risdate>2003</risdate><volume>42</volume><issue>28</issue><spage>5765</spage><epage>5773</epage><pages>5765-5773</pages><issn>1559-128X</issn><issn>0003-6935</issn><eissn>1539-4522</eissn><abstract>A novel, noninvasive measurement technique for quantitative cellular analysis is presented that utilizes the forces generated by an optical beam to evaluate the physical properties of live cells in suspension. In this analysis, a focused, near-infrared laser line with a high cross-sectional intensity gradient is rapidly scanned across a field of cells, and the interaction of those cells with the beam is monitored. The response of each cell to the laser depends on its size, structure, morphology, composition, and surface membrane properties; therefore, with this technique, cell populations of different type, treatment, or biological state can be compared. To demonstrate the utility of this cell analysis platform, we evaluated the early stages of apoptosis induced in the U937 cancer cell line by the drug camptothecin and compared the results with established reference assays. Measurements on our platform show detection of cellular changes earlier than either of the fluorescence-based Annexin V or caspase assays. Because no labeling or additional cell processing is required and because accurate assays can be performed with a small number of cells, this measurement technique may find suitable applications in cell research, medical diagnostics, and drug discovery.</abstract><cop>United States</cop><pmid>14528941</pmid><doi>10.1364/AO.42.005765</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1559-128X
ispartof Applied Optics, 2003-10, Vol.42 (28), p.5765-5773
issn 1559-128X
0003-6935
1539-4522
language eng
recordid cdi_proquest_miscellaneous_75743500
source MEDLINE; Alma/SFX Local Collection; Optica Publishing Group Journals
subjects Apoptosis
Humans
Lasers
Neoplasms - pathology
Neoplasms - physiopathology
Optics and Photonics - instrumentation
Time Factors
Tumor Cells, Cultured
title Optical forces for noninvasive cellular analysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T17%3A47%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Optical%20forces%20for%20noninvasive%20cellular%20analysis&rft.jtitle=Applied%20Optics&rft.au=Wang,%20Mark%20M&rft.date=2003-10-01&rft.volume=42&rft.issue=28&rft.spage=5765&rft.epage=5773&rft.pages=5765-5773&rft.issn=1559-128X&rft.eissn=1539-4522&rft_id=info:doi/10.1364/AO.42.005765&rft_dat=%3Cproquest_cross%3E75743500%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75743500&rft_id=info:pmid/14528941&rfr_iscdi=true