E12 technique: Conventional epoxy resin sheet plastination
Epoxy plastination techniques were developed to obtain thin transparent body slices with high anatomical detail. This is facilitated because the plastinated tissue is transparent and the topography of the anatomical structures well preserved. For this reason, thin epoxy slices are currently used for...
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Veröffentlicht in: | Anatomia, histologia, embryologia histologia, embryologia, 2019-11, Vol.48 (6), p.557-563 |
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creator | Latorre, Rafael Jong, Kees Sora, Mircea‐Constantin López‐Albors, Octavio Baptista, Carlos |
description | Epoxy plastination techniques were developed to obtain thin transparent body slices with high anatomical detail. This is facilitated because the plastinated tissue is transparent and the topography of the anatomical structures well preserved. For this reason, thin epoxy slices are currently used for research purposes in both macroscopic and microscopic studies. The protocol for the conventional epoxy technique (E12) follows the main steps of plastination—specimen preparation, dehydration, impregnation and curing/casting. Preparation begins with selection of the specimen, followed by freezing and slicing. Either fresh or fixed (embalmed) tissue is suitable for epoxy plastination, while slice thickness is kept between 1.5 and 3 mm. Impregnation mixture is made of epoxy E12 resin plus E1 hardener (100 ppw; 28 ppw). This mixture is reactive and temperature sensitive, and for this reason, total impregnation time under vacuum at room laboratory temperature should not last for more than 20–24 hr. Casting of impregnated slices is done in either flat chambers or by the so‐called sandwich method in either fresh mixture or the one used for impregnation. Curing is completed at 40°C to allow a complete polymerization of the epoxy‐mixture. After curing, slices can be photographed, scanned or used for anatomical study under screen negatoscope, magnification glass or fluorescent microscope. Based on epoxy sheet plastination, many anatomical papers have recent observations of and/or clarification of anatomical concepts in different areas of medical expertice. |
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This is facilitated because the plastinated tissue is transparent and the topography of the anatomical structures well preserved. For this reason, thin epoxy slices are currently used for research purposes in both macroscopic and microscopic studies. The protocol for the conventional epoxy technique (E12) follows the main steps of plastination—specimen preparation, dehydration, impregnation and curing/casting. Preparation begins with selection of the specimen, followed by freezing and slicing. Either fresh or fixed (embalmed) tissue is suitable for epoxy plastination, while slice thickness is kept between 1.5 and 3 mm. Impregnation mixture is made of epoxy E12 resin plus E1 hardener (100 ppw; 28 ppw). This mixture is reactive and temperature sensitive, and for this reason, total impregnation time under vacuum at room laboratory temperature should not last for more than 20–24 hr. Casting of impregnated slices is done in either flat chambers or by the so‐called sandwich method in either fresh mixture or the one used for impregnation. Curing is completed at 40°C to allow a complete polymerization of the epoxy‐mixture. After curing, slices can be photographed, scanned or used for anatomical study under screen negatoscope, magnification glass or fluorescent microscope. Based on epoxy sheet plastination, many anatomical papers have recent observations of and/or clarification of anatomical concepts in different areas of medical expertice.</description><identifier>ISSN: 0340-2096</identifier><identifier>EISSN: 1439-0264</identifier><identifier>DOI: 10.1111/ahe.12507</identifier><identifier>PMID: 31617253</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Anatomy ; Anatomy - methods ; Animals ; Dehydration ; E12 technique ; education ; epoxides ; Epoxy Resins ; fluorescence microscopes ; Freezing ; glass ; History, 20th Century ; History, 21st Century ; Humans ; plastination ; Plastination - history ; Plastination - instrumentation ; Plastination - methods ; Polymerization ; sectional anatomy ; slicing ; Specimen preparation ; temperature ; Vacuum</subject><ispartof>Anatomia, histologia, embryologia, 2019-11, Vol.48 (6), p.557-563</ispartof><rights>2019 Blackwell Verlag GmbH</rights><rights>2019 Blackwell Verlag GmbH.</rights><rights>Copyright © 2019 Blackwell Verlag GmbH</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4217-1abb322c6138e20ac4a27e1b193c38a53802d9a521b00be3384fc9cc1a3557673</citedby><cites>FETCH-LOGICAL-c4217-1abb322c6138e20ac4a27e1b193c38a53802d9a521b00be3384fc9cc1a3557673</cites><orcidid>0000-0002-3609-2790 ; 0000-0001-6188-9809</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fahe.12507$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fahe.12507$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31617253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Latorre, Rafael</creatorcontrib><creatorcontrib>Jong, Kees</creatorcontrib><creatorcontrib>Sora, Mircea‐Constantin</creatorcontrib><creatorcontrib>López‐Albors, Octavio</creatorcontrib><creatorcontrib>Baptista, Carlos</creatorcontrib><title>E12 technique: Conventional epoxy resin sheet plastination</title><title>Anatomia, histologia, embryologia</title><addtitle>Anat Histol Embryol</addtitle><description>Epoxy plastination techniques were developed to obtain thin transparent body slices with high anatomical detail. This is facilitated because the plastinated tissue is transparent and the topography of the anatomical structures well preserved. For this reason, thin epoxy slices are currently used for research purposes in both macroscopic and microscopic studies. The protocol for the conventional epoxy technique (E12) follows the main steps of plastination—specimen preparation, dehydration, impregnation and curing/casting. Preparation begins with selection of the specimen, followed by freezing and slicing. Either fresh or fixed (embalmed) tissue is suitable for epoxy plastination, while slice thickness is kept between 1.5 and 3 mm. Impregnation mixture is made of epoxy E12 resin plus E1 hardener (100 ppw; 28 ppw). This mixture is reactive and temperature sensitive, and for this reason, total impregnation time under vacuum at room laboratory temperature should not last for more than 20–24 hr. Casting of impregnated slices is done in either flat chambers or by the so‐called sandwich method in either fresh mixture or the one used for impregnation. Curing is completed at 40°C to allow a complete polymerization of the epoxy‐mixture. After curing, slices can be photographed, scanned or used for anatomical study under screen negatoscope, magnification glass or fluorescent microscope. Based on epoxy sheet plastination, many anatomical papers have recent observations of and/or clarification of anatomical concepts in different areas of medical expertice.</description><subject>Anatomy</subject><subject>Anatomy - methods</subject><subject>Animals</subject><subject>Dehydration</subject><subject>E12 technique</subject><subject>education</subject><subject>epoxides</subject><subject>Epoxy Resins</subject><subject>fluorescence microscopes</subject><subject>Freezing</subject><subject>glass</subject><subject>History, 20th Century</subject><subject>History, 21st Century</subject><subject>Humans</subject><subject>plastination</subject><subject>Plastination - history</subject><subject>Plastination - instrumentation</subject><subject>Plastination - methods</subject><subject>Polymerization</subject><subject>sectional anatomy</subject><subject>slicing</subject><subject>Specimen preparation</subject><subject>temperature</subject><subject>Vacuum</subject><issn>0340-2096</issn><issn>1439-0264</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E1PwkAQBuCN0QiiB_-AaeJFD4WZ2X5yIwTFhMSLnpvtMoSS0tZuq_LvXSh6MDHuZS5P3pl9hbhGGKJ9I7XmIZIP4YnooydjFyjwTkUfpAcuQRz0xIUxG4AAZRyei57EAEPyZV-MZ0hOw3pdZG8tj51pWbxz0WRloXKHq_Jz59RsssIxa-bGqXJlmqxQe3ApzlYqN3x1nAPx-jB7mc7dxfPj03SycLVHGLqo0lQSabs7YgKlPUUhY4qx1DJSvoyAlrHyCVOAlKWMvJWOtUYlfT8MQjkQd11uVZf2RtMk28xoznNVcNmahDyJUUC2gP-phICI4EBvf9FN2db213uFFEEAXmTVfad0XRpT8yqp6myr6l2CkOy7T2z3yaF7a2-OiW265eWP_C7bglEHPrKcd38nJZP5rIv8AuFKigk</recordid><startdate>201911</startdate><enddate>201911</enddate><creator>Latorre, Rafael</creator><creator>Jong, Kees</creator><creator>Sora, Mircea‐Constantin</creator><creator>López‐Albors, Octavio</creator><creator>Baptista, Carlos</creator><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>7TK</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-3609-2790</orcidid><orcidid>https://orcid.org/0000-0001-6188-9809</orcidid></search><sort><creationdate>201911</creationdate><title>E12 technique: Conventional epoxy resin sheet plastination</title><author>Latorre, Rafael ; 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This is facilitated because the plastinated tissue is transparent and the topography of the anatomical structures well preserved. For this reason, thin epoxy slices are currently used for research purposes in both macroscopic and microscopic studies. The protocol for the conventional epoxy technique (E12) follows the main steps of plastination—specimen preparation, dehydration, impregnation and curing/casting. Preparation begins with selection of the specimen, followed by freezing and slicing. Either fresh or fixed (embalmed) tissue is suitable for epoxy plastination, while slice thickness is kept between 1.5 and 3 mm. Impregnation mixture is made of epoxy E12 resin plus E1 hardener (100 ppw; 28 ppw). This mixture is reactive and temperature sensitive, and for this reason, total impregnation time under vacuum at room laboratory temperature should not last for more than 20–24 hr. Casting of impregnated slices is done in either flat chambers or by the so‐called sandwich method in either fresh mixture or the one used for impregnation. Curing is completed at 40°C to allow a complete polymerization of the epoxy‐mixture. After curing, slices can be photographed, scanned or used for anatomical study under screen negatoscope, magnification glass or fluorescent microscope. Based on epoxy sheet plastination, many anatomical papers have recent observations of and/or clarification of anatomical concepts in different areas of medical expertice.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31617253</pmid><doi>10.1111/ahe.12507</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-3609-2790</orcidid><orcidid>https://orcid.org/0000-0001-6188-9809</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anatomy Anatomy - methods Animals Dehydration E12 technique education epoxides Epoxy Resins fluorescence microscopes Freezing glass History, 20th Century History, 21st Century Humans plastination Plastination - history Plastination - instrumentation Plastination - methods Polymerization sectional anatomy slicing Specimen preparation temperature Vacuum |
title | E12 technique: Conventional epoxy resin sheet plastination |
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