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
Hauptverfasser: Mi, Fwu-Long, Huang, Chin-Tsung, Chiu, Ya-Ling, Chen, Mei-Chin, Liang, Hsiang-Fa, Sung, Hsing-Wen
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container_issue 3
container_start_page 667
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). 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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. 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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 &amp; 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 &amp; 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. 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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). 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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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