Implementation of a bimorph-based aperture tapping-SNOM with an incubator to study the evolution of cultured living cells
We present the implementation of a tapping-mode aperture scanning near-field optical microscope (Tapping-SNOM) to a Binder CB incubator (Istituto di Struttura della Materia, Rome, Italy). The microscope operates in the intermittent contact mode using a nonbent optical fibre allowing to reduce the pe...
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Veröffentlicht in: | Journal of microscopy (Oxford) 2008-03, Vol.229 (3), p.433-439 |
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description | We present the implementation of a tapping-mode aperture scanning near-field optical microscope (Tapping-SNOM) to a Binder CB incubator (Istituto di Struttura della Materia, Rome, Italy). The microscope operates in the intermittent contact mode using a nonbent optical fibre allowing to reduce the perturbation exerted on the sample, while the incubator maintains a constant temperature, humidity and CO₂ level. This instrument can maintain and analyse in a controlled environment different samples, both organic and nonorganic. In particular, the Tapping-SNOM can study different cell lines at nanometric resolution and in physiological buffer, following the evolution of the living cells almost indefinitely. We will present several examples of the capabilities of the tapping scanning near-field optical microscope in the study of different lines of living cells, showing corresponding topographical, optical or phase-lag images of the live samples, evidencing the excellent stability, versatility and resolution of the system. |
doi_str_mv | 10.1111/j.1365-2818.2008.01924.x |
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The microscope operates in the intermittent contact mode using a nonbent optical fibre allowing to reduce the perturbation exerted on the sample, while the incubator maintains a constant temperature, humidity and CO₂ level. This instrument can maintain and analyse in a controlled environment different samples, both organic and nonorganic. In particular, the Tapping-SNOM can study different cell lines at nanometric resolution and in physiological buffer, following the evolution of the living cells almost indefinitely. We will present several examples of the capabilities of the tapping scanning near-field optical microscope in the study of different lines of living cells, showing corresponding topographical, optical or phase-lag images of the live samples, evidencing the excellent stability, versatility and resolution of the system.</description><identifier>ISSN: 0022-2720</identifier><identifier>EISSN: 1365-2818</identifier><identifier>DOI: 10.1111/j.1365-2818.2008.01924.x</identifier><identifier>PMID: 18331491</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Cell Line, Tumor - ultrastructure ; Cells, Cultured - ultrastructure ; Endothelial Cells - physiology ; Endothelial Cells - ultrastructure ; Equipment Design ; Erythrocytes - physiology ; Erythrocytes - ultrastructure ; Fiber Optic Technology ; Humans ; Incubator ; Keratinocytes - physiology ; Keratinocytes - ultrastructure ; living cells ; Microscopy, Electron, Scanning - instrumentation ; Microscopy, Electron, Scanning - methods ; Microscopy, Scanning Probe - instrumentation ; Neuroblastoma ; Q-factor ; SNOM ; Super resolution ; Swine ; tapping-mode</subject><ispartof>Journal of microscopy (Oxford), 2008-03, Vol.229 (3), p.433-439</ispartof><rights>2008 The Authors Journal compilation ©2008 The Royal Microscopical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4224-a4470d43d20e70c852d0ea391160ec4e42a855bdefa09f971f295b25940755493</citedby><cites>FETCH-LOGICAL-c4224-a4470d43d20e70c852d0ea391160ec4e42a855bdefa09f971f295b25940755493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2818.2008.01924.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2818.2008.01924.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18331491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LONGO, G</creatorcontrib><creatorcontrib>GIRASOLE, M</creatorcontrib><creatorcontrib>CRICENTI, A</creatorcontrib><title>Implementation of a bimorph-based aperture tapping-SNOM with an incubator to study the evolution of cultured living cells</title><title>Journal of microscopy (Oxford)</title><addtitle>J Microsc</addtitle><description>We present the implementation of a tapping-mode aperture scanning near-field optical microscope (Tapping-SNOM) to a Binder CB incubator (Istituto di Struttura della Materia, Rome, Italy). The microscope operates in the intermittent contact mode using a nonbent optical fibre allowing to reduce the perturbation exerted on the sample, while the incubator maintains a constant temperature, humidity and CO₂ level. This instrument can maintain and analyse in a controlled environment different samples, both organic and nonorganic. In particular, the Tapping-SNOM can study different cell lines at nanometric resolution and in physiological buffer, following the evolution of the living cells almost indefinitely. We will present several examples of the capabilities of the tapping scanning near-field optical microscope in the study of different lines of living cells, showing corresponding topographical, optical or phase-lag images of the live samples, evidencing the excellent stability, versatility and resolution of the system.</description><subject>Animals</subject><subject>Cell Line, Tumor - ultrastructure</subject><subject>Cells, Cultured - ultrastructure</subject><subject>Endothelial Cells - physiology</subject><subject>Endothelial Cells - ultrastructure</subject><subject>Equipment Design</subject><subject>Erythrocytes - physiology</subject><subject>Erythrocytes - ultrastructure</subject><subject>Fiber Optic Technology</subject><subject>Humans</subject><subject>Incubator</subject><subject>Keratinocytes - physiology</subject><subject>Keratinocytes - ultrastructure</subject><subject>living cells</subject><subject>Microscopy, Electron, Scanning - instrumentation</subject><subject>Microscopy, Electron, Scanning - methods</subject><subject>Microscopy, Scanning Probe - instrumentation</subject><subject>Neuroblastoma</subject><subject>Q-factor</subject><subject>SNOM</subject><subject>Super resolution</subject><subject>Swine</subject><subject>tapping-mode</subject><issn>0022-2720</issn><issn>1365-2818</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS0EokPhFcArdgnXf5NkwQJVUAb1Z9F2bTnJTcejJA6203bevg4zwBK8sSV_57tXOoRQBjlL59MuZ2KtMl6yMucAZQ6s4jJ_ekFWfz5ekhUA5xkvOJyQNyHsIJGqhNfkhJVCMFmxFdlvhqnHAcdoonUjdR01tLaD89M2q03AlpoJfZw90mimyY732c3V9SV9tHFLzUjt2My1ic7T6GiIc7uncYsUH1w__zY2c78IWtrbhySgDfZ9eEtedaYP-O54n5K7b19vz75nF9fnm7MvF1kjOZeZkbKAVoqWAxbQlIq3gEZUjK0BG4mSm1KpusXOQNVVBet4pWquKgmFUrISp-TjwTt593PGEPVgw7KBGdHNQRcgkpSX_wSF5GsAJRJYHsDGuxA8dnrydjB-rxnopR-900sNeqlBL_3oX_3opxR9f5wx1wO2f4PHQhLw-QA82h73_y3WPy43yyvlPxzynXHa3Hsb9N0NByYSvC6qNOYZfimoPg</recordid><startdate>200803</startdate><enddate>200803</enddate><creator>LONGO, G</creator><creator>GIRASOLE, M</creator><creator>CRICENTI, A</creator><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><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>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>200803</creationdate><title>Implementation of a bimorph-based aperture tapping-SNOM with an incubator to study the evolution of cultured living cells</title><author>LONGO, G ; GIRASOLE, M ; CRICENTI, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4224-a4470d43d20e70c852d0ea391160ec4e42a855bdefa09f971f295b25940755493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Cell Line, Tumor - ultrastructure</topic><topic>Cells, Cultured - ultrastructure</topic><topic>Endothelial Cells - physiology</topic><topic>Endothelial Cells - ultrastructure</topic><topic>Equipment Design</topic><topic>Erythrocytes - physiology</topic><topic>Erythrocytes - ultrastructure</topic><topic>Fiber Optic Technology</topic><topic>Humans</topic><topic>Incubator</topic><topic>Keratinocytes - physiology</topic><topic>Keratinocytes - ultrastructure</topic><topic>living cells</topic><topic>Microscopy, Electron, Scanning - instrumentation</topic><topic>Microscopy, Electron, Scanning - methods</topic><topic>Microscopy, Scanning Probe - instrumentation</topic><topic>Neuroblastoma</topic><topic>Q-factor</topic><topic>SNOM</topic><topic>Super resolution</topic><topic>Swine</topic><topic>tapping-mode</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LONGO, G</creatorcontrib><creatorcontrib>GIRASOLE, M</creatorcontrib><creatorcontrib>CRICENTI, A</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of microscopy (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LONGO, G</au><au>GIRASOLE, M</au><au>CRICENTI, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Implementation of a bimorph-based aperture tapping-SNOM with an incubator to study the evolution of cultured living cells</atitle><jtitle>Journal of microscopy (Oxford)</jtitle><addtitle>J Microsc</addtitle><date>2008-03</date><risdate>2008</risdate><volume>229</volume><issue>3</issue><spage>433</spage><epage>439</epage><pages>433-439</pages><issn>0022-2720</issn><eissn>1365-2818</eissn><abstract>We present the implementation of a tapping-mode aperture scanning near-field optical microscope (Tapping-SNOM) to a Binder CB incubator (Istituto di Struttura della Materia, Rome, Italy). The microscope operates in the intermittent contact mode using a nonbent optical fibre allowing to reduce the perturbation exerted on the sample, while the incubator maintains a constant temperature, humidity and CO₂ level. This instrument can maintain and analyse in a controlled environment different samples, both organic and nonorganic. In particular, the Tapping-SNOM can study different cell lines at nanometric resolution and in physiological buffer, following the evolution of the living cells almost indefinitely. 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subjects | Animals Cell Line, Tumor - ultrastructure Cells, Cultured - ultrastructure Endothelial Cells - physiology Endothelial Cells - ultrastructure Equipment Design Erythrocytes - physiology Erythrocytes - ultrastructure Fiber Optic Technology Humans Incubator Keratinocytes - physiology Keratinocytes - ultrastructure living cells Microscopy, Electron, Scanning - instrumentation Microscopy, Electron, Scanning - methods Microscopy, Scanning Probe - instrumentation Neuroblastoma Q-factor SNOM Super resolution Swine tapping-mode |
title | Implementation of a bimorph-based aperture tapping-SNOM with an incubator to study the evolution of cultured living cells |
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