Aglycone geniposidic acid, a naturally occurring crosslinking agent, and its application for the fixation of collagenous tissues
A natural compound, aglycone geniposidic acid (aGSA), originated from the fruits of Gardenia jasminoides ELLIS was used for the fixation of collagenous tissues. The presumed crosslinking reaction mechanism of collagenous tissues with aGSA was inferred by reacting aGSA with a bifunctional amine, 1,6‐...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2007-12, Vol.83A (3), p.667-673 |
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container_title | Journal of biomedical materials research. Part A |
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creator | Mi, Fwu-Long Huang, Chin-Tsung Chiu, Ya-Ling Chen, Mei-Chin Liang, Hsiang-Fa Sung, Hsing-Wen |
description | A natural compound, aglycone geniposidic acid (aGSA), originated from the fruits of Gardenia jasminoides ELLIS was used for the fixation of collagenous tissues. The presumed crosslinking reaction mechanism of collagenous tissues with aGSA was inferred by reacting aGSA with a bifunctional amine, 1,6‐hexanediamine, using a series of 1H NMR, FT‐IR, and UV/Vis spectra analyses. aGSA reacted with 1,6‐hexanediamine by a nucleophilic attack on the olefinic carbon atom at C‐2 of deoxyloganin aglycone, followed by opening the dihydropyran ring to form heterocyclic amine compounds. It is inferred that aGSA may form intramolecular and intermolecular crosslinks with a heterocyclic structure within collagen fibers in tissues. The degrees of tissue fixation by aGSA at different pH values were investigated by examining the fixation indices and denaturation temperatures of test samples. It was found that the fixation indices and denaturation temperatures of test samples fixed at neutral or basic pH (pH 7.4 or pH 8.5) were significantly greater than at acidic pH (pH 4.0). The results obtained in this study may be used to elucidate the crosslinking mechanism and optimize the fixation process for developing bioprostheses fixed by aGSA. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res 2007 |
doi_str_mv | 10.1002/jbm.a.31274 |
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The presumed crosslinking reaction mechanism of collagenous tissues with aGSA was inferred by reacting aGSA with a bifunctional amine, 1,6‐hexanediamine, using a series of 1H NMR, FT‐IR, and UV/Vis spectra analyses. aGSA reacted with 1,6‐hexanediamine by a nucleophilic attack on the olefinic carbon atom at C‐2 of deoxyloganin aglycone, followed by opening the dihydropyran ring to form heterocyclic amine compounds. It is inferred that aGSA may form intramolecular and intermolecular crosslinks with a heterocyclic structure within collagen fibers in tissues. The degrees of tissue fixation by aGSA at different pH values were investigated by examining the fixation indices and denaturation temperatures of test samples. It was found that the fixation indices and denaturation temperatures of test samples fixed at neutral or basic pH (pH 7.4 or pH 8.5) were significantly greater than at acidic pH (pH 4.0). The results obtained in this study may be used to elucidate the crosslinking mechanism and optimize the fixation process for developing bioprostheses fixed by aGSA. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res 2007</description><identifier>ISSN: 1549-3296</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.31274</identifier><identifier>PMID: 17530623</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>aglycone geniposidic acid ; Bioprosthesis ; collagen ; Collagen - chemistry ; collagenous tissue ; Cross-Linking Reagents - chemistry ; crosslinking agent ; Gardenia - chemistry ; Glucosides - chemical synthesis ; Glucosides - chemistry ; Hydrogen-Ion Concentration ; Iridoid Glucosides ; Iridoids - chemical synthesis ; Iridoids - chemistry ; Tissue Adhesives - chemistry</subject><ispartof>Journal of biomedical materials research. Part A, 2007-12, Vol.83A (3), p.667-673</ispartof><rights>Copyright © 2007 Wiley Periodicals, Inc.</rights><rights>Copyright 2007 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3984-cce3ba6fff12be92fbb34e218ba44ef8d6c73984a130925e4e204d003bcd9fbc3</citedby><cites>FETCH-LOGICAL-c3984-cce3ba6fff12be92fbb34e218ba44ef8d6c73984a130925e4e204d003bcd9fbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbm.a.31274$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbm.a.31274$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17530623$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mi, Fwu-Long</creatorcontrib><creatorcontrib>Huang, Chin-Tsung</creatorcontrib><creatorcontrib>Chiu, Ya-Ling</creatorcontrib><creatorcontrib>Chen, Mei-Chin</creatorcontrib><creatorcontrib>Liang, Hsiang-Fa</creatorcontrib><creatorcontrib>Sung, Hsing-Wen</creatorcontrib><title>Aglycone geniposidic acid, a naturally occurring crosslinking agent, and its application for the fixation of collagenous tissues</title><title>Journal of biomedical materials research. Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>A natural compound, aglycone geniposidic acid (aGSA), originated from the fruits of Gardenia jasminoides ELLIS was used for the fixation of collagenous tissues. The presumed crosslinking reaction mechanism of collagenous tissues with aGSA was inferred by reacting aGSA with a bifunctional amine, 1,6‐hexanediamine, using a series of 1H NMR, FT‐IR, and UV/Vis spectra analyses. aGSA reacted with 1,6‐hexanediamine by a nucleophilic attack on the olefinic carbon atom at C‐2 of deoxyloganin aglycone, followed by opening the dihydropyran ring to form heterocyclic amine compounds. It is inferred that aGSA may form intramolecular and intermolecular crosslinks with a heterocyclic structure within collagen fibers in tissues. The degrees of tissue fixation by aGSA at different pH values were investigated by examining the fixation indices and denaturation temperatures of test samples. It was found that the fixation indices and denaturation temperatures of test samples fixed at neutral or basic pH (pH 7.4 or pH 8.5) were significantly greater than at acidic pH (pH 4.0). The results obtained in this study may be used to elucidate the crosslinking mechanism and optimize the fixation process for developing bioprostheses fixed by aGSA. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res 2007</description><subject>aglycone geniposidic acid</subject><subject>Bioprosthesis</subject><subject>collagen</subject><subject>Collagen - chemistry</subject><subject>collagenous tissue</subject><subject>Cross-Linking Reagents - chemistry</subject><subject>crosslinking agent</subject><subject>Gardenia - chemistry</subject><subject>Glucosides - chemical synthesis</subject><subject>Glucosides - chemistry</subject><subject>Hydrogen-Ion Concentration</subject><subject>Iridoid Glucosides</subject><subject>Iridoids - chemical synthesis</subject><subject>Iridoids - chemistry</subject><subject>Tissue Adhesives - chemistry</subject><issn>1549-3296</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EoqV0xR55xQYy-BUnWbbT0odKqdRWLC3bsQe3njjYiejs-Ok4zRR2VF5c-_o7x1c-ALzDaIERIp_v1HohFxSTir0Au7gsScEaXr6c9qwpKGn4DniT0l2GOSrJa7CDq5IiTugu-H2w8hsdOgNXpnN9SK51Gkrt2k9Qwk4OY5Teb2DQeozRdSuoY0jJu-5-OsisGjLZtdANCcq-907LwYUO2hDh8MNA6x7mRrBQB-8nSRgTHFxKo0lvwSsrfTL727oHbr8c3yxPi4tvJ2fLg4tC06ZmhdaGKsmttZgo0xCrFGWG4FpJxoytW66rCZSYooaUJt8h1iJElW4bqzTdAx9m3z6Gn_ndQaxd0ibP05k8juA14w3h9bNg9i9JXhn8OIOPPxKNFX10axk3AiMxJSNyMkKKx2Qy_X5rO6q1af-x2ygygGfgl_Nm8z8vcX749cm0mDUuDebhr0bGe8ErWpXi--WJIEc1JVfnS3FN_wCGC6tN</recordid><startdate>20071201</startdate><enddate>20071201</enddate><creator>Mi, Fwu-Long</creator><creator>Huang, Chin-Tsung</creator><creator>Chiu, Ya-Ling</creator><creator>Chen, Mei-Chin</creator><creator>Liang, Hsiang-Fa</creator><creator>Sung, Hsing-Wen</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20071201</creationdate><title>Aglycone geniposidic acid, a naturally occurring crosslinking agent, and its application for the fixation of collagenous tissues</title><author>Mi, Fwu-Long ; Huang, Chin-Tsung ; Chiu, Ya-Ling ; Chen, Mei-Chin ; Liang, Hsiang-Fa ; Sung, Hsing-Wen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3984-cce3ba6fff12be92fbb34e218ba44ef8d6c73984a130925e4e204d003bcd9fbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>aglycone geniposidic acid</topic><topic>Bioprosthesis</topic><topic>collagen</topic><topic>Collagen - chemistry</topic><topic>collagenous tissue</topic><topic>Cross-Linking Reagents - chemistry</topic><topic>crosslinking agent</topic><topic>Gardenia - chemistry</topic><topic>Glucosides - chemical synthesis</topic><topic>Glucosides - chemistry</topic><topic>Hydrogen-Ion Concentration</topic><topic>Iridoid Glucosides</topic><topic>Iridoids - chemical synthesis</topic><topic>Iridoids - chemistry</topic><topic>Tissue Adhesives - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mi, Fwu-Long</creatorcontrib><creatorcontrib>Huang, Chin-Tsung</creatorcontrib><creatorcontrib>Chiu, Ya-Ling</creatorcontrib><creatorcontrib>Chen, Mei-Chin</creatorcontrib><creatorcontrib>Liang, Hsiang-Fa</creatorcontrib><creatorcontrib>Sung, Hsing-Wen</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomedical materials research. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mi, Fwu-Long</au><au>Huang, Chin-Tsung</au><au>Chiu, Ya-Ling</au><au>Chen, Mei-Chin</au><au>Liang, Hsiang-Fa</au><au>Sung, Hsing-Wen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aglycone geniposidic acid, a naturally occurring crosslinking agent, and its application for the fixation of collagenous tissues</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2007-12-01</date><risdate>2007</risdate><volume>83A</volume><issue>3</issue><spage>667</spage><epage>673</epage><pages>667-673</pages><issn>1549-3296</issn><eissn>1552-4965</eissn><abstract>A natural compound, aglycone geniposidic acid (aGSA), originated from the fruits of Gardenia jasminoides ELLIS was used for the fixation of collagenous tissues. The presumed crosslinking reaction mechanism of collagenous tissues with aGSA was inferred by reacting aGSA with a bifunctional amine, 1,6‐hexanediamine, using a series of 1H NMR, FT‐IR, and UV/Vis spectra analyses. aGSA reacted with 1,6‐hexanediamine by a nucleophilic attack on the olefinic carbon atom at C‐2 of deoxyloganin aglycone, followed by opening the dihydropyran ring to form heterocyclic amine compounds. It is inferred that aGSA may form intramolecular and intermolecular crosslinks with a heterocyclic structure within collagen fibers in tissues. The degrees of tissue fixation by aGSA at different pH values were investigated by examining the fixation indices and denaturation temperatures of test samples. It was found that the fixation indices and denaturation temperatures of test samples fixed at neutral or basic pH (pH 7.4 or pH 8.5) were significantly greater than at acidic pH (pH 4.0). The results obtained in this study may be used to elucidate the crosslinking mechanism and optimize the fixation process for developing bioprostheses fixed by aGSA. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res 2007</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17530623</pmid><doi>10.1002/jbm.a.31274</doi><tpages>7</tpages></addata></record> |
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subjects | aglycone geniposidic acid Bioprosthesis collagen Collagen - chemistry collagenous tissue Cross-Linking Reagents - chemistry crosslinking agent Gardenia - chemistry Glucosides - chemical synthesis Glucosides - chemistry Hydrogen-Ion Concentration Iridoid Glucosides Iridoids - chemical synthesis Iridoids - chemistry Tissue Adhesives - chemistry |
title | Aglycone geniposidic acid, a naturally occurring crosslinking agent, and its application for the fixation of collagenous tissues |
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