Analyzing the feasibility of discriminating between collagen types I and II using polarization‐resolved second harmonic generation
According to previous studies, the nonlinear susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation (P‐SHG) under the assumption of cylindrical symmetry can be used to distinguish between fibrillar collagen types. Discriminating between collagen fibrils of...
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Veröffentlicht in: | Journal of biophotonics 2019-01, Vol.12 (1), p.e201800090-n/a |
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description | According to previous studies, the nonlinear susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation (P‐SHG) under the assumption of cylindrical symmetry can be used to distinguish between fibrillar collagen types. Discriminating between collagen fibrils of types I and II is important in tissue engineering of cartilage. However, cartilage has a random organization of collagen fibrils, and the assumption of cylindrical symmetry may be incorrect. In this study, we simulated the P‐SHG response from different collagen organizations and demonstrated a possible method to exclude areas where cylindrical symmetry is not fulfilled and where fibrils are located in the imaging plane. The χ33/χ31‐ratio for collagen type I in tendon and collagen type II in cartilage was estimated to be 1.33 and 1.36, respectively, using this method. These ratios are now much closer than what has been reported previously in the literature, and the larger reported differences between collagen types can be explained by variation in the structural organization.
According to previous studies, the susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation, assuming cylindrical symmetry, can be used to distinguish collagen types. In this study, we demonstrate a method of excluding regions that do not fulfill cylindrical symmetry. Thereby, the lowest χ33/χ31‐value is unaffected by orientation. However, the results indicate that the χ33/χ31‐values for collagen types I and II are very close and difficult to distinguish. |
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According to previous studies, the susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation, assuming cylindrical symmetry, can be used to distinguish collagen types. In this study, we demonstrate a method of excluding regions that do not fulfill cylindrical symmetry. Thereby, the lowest χ33/χ31‐value is unaffected by orientation. However, the results indicate that the χ33/χ31‐values for collagen types I and II are very close and difficult to distinguish.</description><identifier>ISSN: 1864-063X</identifier><identifier>EISSN: 1864-0648</identifier><identifier>DOI: 10.1002/jbio.201800090</identifier><identifier>PMID: 29971934</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH & Co. KGaA</publisher><subject>Animals ; Cartilage ; Cartilage - metabolism ; Chickens ; Collagen ; Collagen (type I) ; Collagen (type II) ; Collagen Type I - chemistry ; Collagen Type I - metabolism ; Collagen Type II - chemistry ; Collagen Type II - metabolism ; Feasibility Studies ; Fibrils ; Nonlinear Dynamics ; nonlinear optical microscopy ; Optical Phenomena ; Polarization ; Second harmonic generation ; second harmonic generation microscopy ; Swine ; Symmetry ; tendon ; Tendons - metabolism ; Tensors ; Tissue engineering</subject><ispartof>Journal of biophotonics, 2019-01, Vol.12 (1), p.e201800090-n/a</ispartof><rights>2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4130-953746d39a6fa25e63e5619906705b9487eed7c1881cd89c2759b190896be8003</citedby><cites>FETCH-LOGICAL-c4130-953746d39a6fa25e63e5619906705b9487eed7c1881cd89c2759b190896be8003</cites><orcidid>0000-0001-6303-859X ; 0000-0002-5296-4501 ; 0000-0002-5404-2033</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbio.201800090$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbio.201800090$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29971934$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Romijn, Elisabeth I.</creatorcontrib><creatorcontrib>Finnøy, Andreas</creatorcontrib><creatorcontrib>Lilledahl, Magnus B.</creatorcontrib><title>Analyzing the feasibility of discriminating between collagen types I and II using polarization‐resolved second harmonic generation</title><title>Journal of biophotonics</title><addtitle>J Biophotonics</addtitle><description>According to previous studies, the nonlinear susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation (P‐SHG) under the assumption of cylindrical symmetry can be used to distinguish between fibrillar collagen types. Discriminating between collagen fibrils of types I and II is important in tissue engineering of cartilage. However, cartilage has a random organization of collagen fibrils, and the assumption of cylindrical symmetry may be incorrect. In this study, we simulated the P‐SHG response from different collagen organizations and demonstrated a possible method to exclude areas where cylindrical symmetry is not fulfilled and where fibrils are located in the imaging plane. The χ33/χ31‐ratio for collagen type I in tendon and collagen type II in cartilage was estimated to be 1.33 and 1.36, respectively, using this method. These ratios are now much closer than what has been reported previously in the literature, and the larger reported differences between collagen types can be explained by variation in the structural organization.
According to previous studies, the susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation, assuming cylindrical symmetry, can be used to distinguish collagen types. In this study, we demonstrate a method of excluding regions that do not fulfill cylindrical symmetry. Thereby, the lowest χ33/χ31‐value is unaffected by orientation. However, the results indicate that the χ33/χ31‐values for collagen types I and II are very close and difficult to distinguish.</description><subject>Animals</subject><subject>Cartilage</subject><subject>Cartilage - metabolism</subject><subject>Chickens</subject><subject>Collagen</subject><subject>Collagen (type I)</subject><subject>Collagen (type II)</subject><subject>Collagen Type I - chemistry</subject><subject>Collagen Type I - metabolism</subject><subject>Collagen Type II - chemistry</subject><subject>Collagen Type II - metabolism</subject><subject>Feasibility Studies</subject><subject>Fibrils</subject><subject>Nonlinear Dynamics</subject><subject>nonlinear optical microscopy</subject><subject>Optical Phenomena</subject><subject>Polarization</subject><subject>Second harmonic generation</subject><subject>second harmonic generation microscopy</subject><subject>Swine</subject><subject>Symmetry</subject><subject>tendon</subject><subject>Tendons - metabolism</subject><subject>Tensors</subject><subject>Tissue engineering</subject><issn>1864-063X</issn><issn>1864-0648</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1P3DAQhq2qVflorz1Wlnrhsss4dhz7CIhCEBKXVuotcpwJeJWNt3YCCqce-gP6G_kleFnYSlw4zRyeeaR5X0K-MJgzgOxwUTs_z4ApANDwjuwyJcUMpFDvtzv_tUP2YlwASOA5_0h2Mq0LprnYJX-PetNN966_psMN0hZNdLXr3DBR39LGRRvc0vVmWBM1DneIPbW-68x1WoZphZGW1PQNLUs6xjW18p0J7j6d-P7hz7-A0Xe32NCI1ifuxoSl752lSYDhifpEPrSmi_j5ee6Tn99Pf5yczy6vzsqTo8uZFYzDTOe8ELLh2sjWZDlKjrlkWoMsIK-1UAViU1imFLON0jYrcl0zDUrLGlNAfJ8cbLyr4H-PGIdqmR7E9EyPfoxVlnLLhFagE_rtFbrwY0hZJYpJIQolc5mo-YaywccYsK1WKS4TpopBte6nWvdTbftJB1-ftWO9xGaLvxSSAL0B7lyH0xu66uK4vPovfwQzB56A</recordid><startdate>201901</startdate><enddate>201901</enddate><creator>Romijn, Elisabeth I.</creator><creator>Finnøy, Andreas</creator><creator>Lilledahl, Magnus B.</creator><general>WILEY‐VCH Verlag GmbH & Co. KGaA</general><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>7QO</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>K9.</scope><scope>L7M</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6303-859X</orcidid><orcidid>https://orcid.org/0000-0002-5296-4501</orcidid><orcidid>https://orcid.org/0000-0002-5404-2033</orcidid></search><sort><creationdate>201901</creationdate><title>Analyzing the feasibility of discriminating between collagen types I and II using polarization‐resolved second harmonic generation</title><author>Romijn, Elisabeth I. ; Finnøy, Andreas ; Lilledahl, Magnus B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4130-953746d39a6fa25e63e5619906705b9487eed7c1881cd89c2759b190896be8003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Cartilage</topic><topic>Cartilage - metabolism</topic><topic>Chickens</topic><topic>Collagen</topic><topic>Collagen (type I)</topic><topic>Collagen (type II)</topic><topic>Collagen Type I - chemistry</topic><topic>Collagen Type I - metabolism</topic><topic>Collagen Type II - chemistry</topic><topic>Collagen Type II - metabolism</topic><topic>Feasibility Studies</topic><topic>Fibrils</topic><topic>Nonlinear Dynamics</topic><topic>nonlinear optical microscopy</topic><topic>Optical Phenomena</topic><topic>Polarization</topic><topic>Second harmonic generation</topic><topic>second harmonic generation microscopy</topic><topic>Swine</topic><topic>Symmetry</topic><topic>tendon</topic><topic>Tendons - metabolism</topic><topic>Tensors</topic><topic>Tissue engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Romijn, Elisabeth I.</creatorcontrib><creatorcontrib>Finnøy, Andreas</creatorcontrib><creatorcontrib>Lilledahl, Magnus B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biophotonics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Romijn, Elisabeth I.</au><au>Finnøy, Andreas</au><au>Lilledahl, Magnus B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analyzing the feasibility of discriminating between collagen types I and II using polarization‐resolved second harmonic generation</atitle><jtitle>Journal of biophotonics</jtitle><addtitle>J Biophotonics</addtitle><date>2019-01</date><risdate>2019</risdate><volume>12</volume><issue>1</issue><spage>e201800090</spage><epage>n/a</epage><pages>e201800090-n/a</pages><issn>1864-063X</issn><eissn>1864-0648</eissn><abstract>According to previous studies, the nonlinear susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation (P‐SHG) under the assumption of cylindrical symmetry can be used to distinguish between fibrillar collagen types. Discriminating between collagen fibrils of types I and II is important in tissue engineering of cartilage. However, cartilage has a random organization of collagen fibrils, and the assumption of cylindrical symmetry may be incorrect. In this study, we simulated the P‐SHG response from different collagen organizations and demonstrated a possible method to exclude areas where cylindrical symmetry is not fulfilled and where fibrils are located in the imaging plane. The χ33/χ31‐ratio for collagen type I in tendon and collagen type II in cartilage was estimated to be 1.33 and 1.36, respectively, using this method. These ratios are now much closer than what has been reported previously in the literature, and the larger reported differences between collagen types can be explained by variation in the structural organization.
According to previous studies, the susceptibility tensor ratio χ33/χ31 obtained from polarization‐resolved second harmonic generation, assuming cylindrical symmetry, can be used to distinguish collagen types. In this study, we demonstrate a method of excluding regions that do not fulfill cylindrical symmetry. Thereby, the lowest χ33/χ31‐value is unaffected by orientation. However, the results indicate that the χ33/χ31‐values for collagen types I and II are very close and difficult to distinguish.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH & Co. KGaA</pub><pmid>29971934</pmid><doi>10.1002/jbio.201800090</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6303-859X</orcidid><orcidid>https://orcid.org/0000-0002-5296-4501</orcidid><orcidid>https://orcid.org/0000-0002-5404-2033</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cartilage Cartilage - metabolism Chickens Collagen Collagen (type I) Collagen (type II) Collagen Type I - chemistry Collagen Type I - metabolism Collagen Type II - chemistry Collagen Type II - metabolism Feasibility Studies Fibrils Nonlinear Dynamics nonlinear optical microscopy Optical Phenomena Polarization Second harmonic generation second harmonic generation microscopy Swine Symmetry tendon Tendons - metabolism Tensors Tissue engineering |
title | Analyzing the feasibility of discriminating between collagen types I and II using polarization‐resolved second harmonic generation |
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