Diaminopropionic Acid Reinforced Graphene Sponge and Its Use for Hemostasis
2,3-Diaminopropionic acid (DapA), a medicinal amino acid, is used for the first time to prepare a DapA cross-linked graphene sponge (DCGS) for hemostasis treatment. In a comparison with the reported ethanediamine (EDA) cross-linked graphene sponge (CGS), this carboxyl-functionalized DCGS can not onl...
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Veröffentlicht in: | ACS applied materials & interfaces 2016-03, Vol.8 (12), p.7666-7673 |
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description | 2,3-Diaminopropionic acid (DapA), a medicinal amino acid, is used for the first time to prepare a DapA cross-linked graphene sponge (DCGS) for hemostasis treatment. In a comparison with the reported ethanediamine (EDA) cross-linked graphene sponge (CGS), this carboxyl-functionalized DCGS can not only quickly absorb plasma, but also stimulate erythrocytes and platelets to change their normal form and structure at the interface, which largely affects a cell’s metabolism and biofunction, thus further promoting blood coagulation. Whole blood clotting and rat-tail amputation tests indicated that on the basis of the additional interfacial stimulation, the hemostatic efficiency of the DCGS has been significantly improved in comparison with that of the CGS control (P < 0.05). In-depth insight revealed that the increased oxidation degree and the negative charge density play the crucial rule in the enhanced hemostatic performance. The chiral effect contributes mainly to the selective adhesion of erythrocytes and platelets rather than practical hemostasis. Nevertheless, this presentation demonstrated that, on the premise of keeping the fast absorbability, this is an effective method to improve the hemostatic efficiency by enhancing the cell/graphene interface interaction. |
doi_str_mv | 10.1021/acsami.5b12715 |
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In a comparison with the reported ethanediamine (EDA) cross-linked graphene sponge (CGS), this carboxyl-functionalized DCGS can not only quickly absorb plasma, but also stimulate erythrocytes and platelets to change their normal form and structure at the interface, which largely affects a cell’s metabolism and biofunction, thus further promoting blood coagulation. Whole blood clotting and rat-tail amputation tests indicated that on the basis of the additional interfacial stimulation, the hemostatic efficiency of the DCGS has been significantly improved in comparison with that of the CGS control (P < 0.05). In-depth insight revealed that the increased oxidation degree and the negative charge density play the crucial rule in the enhanced hemostatic performance. The chiral effect contributes mainly to the selective adhesion of erythrocytes and platelets rather than practical hemostasis. Nevertheless, this presentation demonstrated that, on the premise of keeping the fast absorbability, this is an effective method to improve the hemostatic efficiency by enhancing the cell/graphene interface interaction.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.5b12715</identifier><identifier>PMID: 26978481</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Anticoagulants - chemistry ; Anticoagulants - pharmacology ; beta-Alanine - analogs & derivatives ; beta-Alanine - chemistry ; beta-Alanine - pharmacology ; Cell Adhesion - drug effects ; Erythrocytes - metabolism ; Erythrocytes - ultrastructure ; Graphite - chemistry ; Graphite - pharmacology ; Hemostasis - drug effects ; Rats ; Rats, Sprague-Dawley</subject><ispartof>ACS applied materials & interfaces, 2016-03, Vol.8 (12), p.7666-7673</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a396t-ff311dc01b637b3ee681492f1148c7579de3ca4d763f1b26351e81cbdc5fa38f3</citedby><cites>FETCH-LOGICAL-a396t-ff311dc01b637b3ee681492f1148c7579de3ca4d763f1b26351e81cbdc5fa38f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.5b12715$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.5b12715$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26978481$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quan, Kecheng</creatorcontrib><creatorcontrib>Li, Guofeng</creatorcontrib><creatorcontrib>Tao, Lei</creatorcontrib><creatorcontrib>Xie, Qian</creatorcontrib><creatorcontrib>Yuan, Qipeng</creatorcontrib><creatorcontrib>Wang, Xing</creatorcontrib><title>Diaminopropionic Acid Reinforced Graphene Sponge and Its Use for Hemostasis</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>2,3-Diaminopropionic acid (DapA), a medicinal amino acid, is used for the first time to prepare a DapA cross-linked graphene sponge (DCGS) for hemostasis treatment. In a comparison with the reported ethanediamine (EDA) cross-linked graphene sponge (CGS), this carboxyl-functionalized DCGS can not only quickly absorb plasma, but also stimulate erythrocytes and platelets to change their normal form and structure at the interface, which largely affects a cell’s metabolism and biofunction, thus further promoting blood coagulation. Whole blood clotting and rat-tail amputation tests indicated that on the basis of the additional interfacial stimulation, the hemostatic efficiency of the DCGS has been significantly improved in comparison with that of the CGS control (P < 0.05). In-depth insight revealed that the increased oxidation degree and the negative charge density play the crucial rule in the enhanced hemostatic performance. The chiral effect contributes mainly to the selective adhesion of erythrocytes and platelets rather than practical hemostasis. Nevertheless, this presentation demonstrated that, on the premise of keeping the fast absorbability, this is an effective method to improve the hemostatic efficiency by enhancing the cell/graphene interface interaction.</description><subject>Animals</subject><subject>Anticoagulants - chemistry</subject><subject>Anticoagulants - pharmacology</subject><subject>beta-Alanine - analogs & derivatives</subject><subject>beta-Alanine - chemistry</subject><subject>beta-Alanine - pharmacology</subject><subject>Cell Adhesion - drug effects</subject><subject>Erythrocytes - metabolism</subject><subject>Erythrocytes - ultrastructure</subject><subject>Graphite - chemistry</subject><subject>Graphite - pharmacology</subject><subject>Hemostasis - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kDFPwzAQRi0EoqWwMiKPCCklFzuxM1YF2opKSEBny3HO4KqJQ5wM_HuCWrox3Q3v-3T3CLmGeApxAvfaBF25aVpAIiA9IWPIOY9kkianx53zEbkIYRvHGUvi9JyMkiwXkksYk-cHN-Rr37S-cb52hs6MK-krutr61mBJF61uPrFG-tb4-gOprku66gLdBKQDQpdY-dDp4MIlObN6F_DqMCdk8_T4Pl9G65fFaj5bR5rlWRdZywBKE0ORMVEwxEwCzxMLwKURqchLZEbzUmTMQpFkLAWUYIrSpFYzadmE3O57h6O_egydqlwwuNvpGn0fFAghuBR5Lgd0ukdN60No0aqmdZVuvxXE6leg2gtUB4FD4ObQ3RcVlkf8z9gA3O2BIai2vm_r4dX_2n4Akat6vQ</recordid><startdate>20160330</startdate><enddate>20160330</enddate><creator>Quan, Kecheng</creator><creator>Li, Guofeng</creator><creator>Tao, Lei</creator><creator>Xie, Qian</creator><creator>Yuan, Qipeng</creator><creator>Wang, Xing</creator><general>American Chemical Society</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>7X8</scope></search><sort><creationdate>20160330</creationdate><title>Diaminopropionic Acid Reinforced Graphene Sponge and Its Use for Hemostasis</title><author>Quan, Kecheng ; Li, Guofeng ; Tao, Lei ; Xie, Qian ; Yuan, Qipeng ; Wang, Xing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a396t-ff311dc01b637b3ee681492f1148c7579de3ca4d763f1b26351e81cbdc5fa38f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Anticoagulants - chemistry</topic><topic>Anticoagulants - pharmacology</topic><topic>beta-Alanine - analogs & derivatives</topic><topic>beta-Alanine - chemistry</topic><topic>beta-Alanine - pharmacology</topic><topic>Cell Adhesion - drug effects</topic><topic>Erythrocytes - metabolism</topic><topic>Erythrocytes - ultrastructure</topic><topic>Graphite - chemistry</topic><topic>Graphite - pharmacology</topic><topic>Hemostasis - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quan, Kecheng</creatorcontrib><creatorcontrib>Li, Guofeng</creatorcontrib><creatorcontrib>Tao, Lei</creatorcontrib><creatorcontrib>Xie, Qian</creatorcontrib><creatorcontrib>Yuan, Qipeng</creatorcontrib><creatorcontrib>Wang, Xing</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quan, Kecheng</au><au>Li, Guofeng</au><au>Tao, Lei</au><au>Xie, Qian</au><au>Yuan, Qipeng</au><au>Wang, Xing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diaminopropionic Acid Reinforced Graphene Sponge and Its Use for Hemostasis</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2016-03-30</date><risdate>2016</risdate><volume>8</volume><issue>12</issue><spage>7666</spage><epage>7673</epage><pages>7666-7673</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>2,3-Diaminopropionic acid (DapA), a medicinal amino acid, is used for the first time to prepare a DapA cross-linked graphene sponge (DCGS) for hemostasis treatment. In a comparison with the reported ethanediamine (EDA) cross-linked graphene sponge (CGS), this carboxyl-functionalized DCGS can not only quickly absorb plasma, but also stimulate erythrocytes and platelets to change their normal form and structure at the interface, which largely affects a cell’s metabolism and biofunction, thus further promoting blood coagulation. Whole blood clotting and rat-tail amputation tests indicated that on the basis of the additional interfacial stimulation, the hemostatic efficiency of the DCGS has been significantly improved in comparison with that of the CGS control (P < 0.05). In-depth insight revealed that the increased oxidation degree and the negative charge density play the crucial rule in the enhanced hemostatic performance. The chiral effect contributes mainly to the selective adhesion of erythrocytes and platelets rather than practical hemostasis. Nevertheless, this presentation demonstrated that, on the premise of keeping the fast absorbability, this is an effective method to improve the hemostatic efficiency by enhancing the cell/graphene interface interaction.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>26978481</pmid><doi>10.1021/acsami.5b12715</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Anticoagulants - chemistry Anticoagulants - pharmacology beta-Alanine - analogs & derivatives beta-Alanine - chemistry beta-Alanine - pharmacology Cell Adhesion - drug effects Erythrocytes - metabolism Erythrocytes - ultrastructure Graphite - chemistry Graphite - pharmacology Hemostasis - drug effects Rats Rats, Sprague-Dawley |
title | Diaminopropionic Acid Reinforced Graphene Sponge and Its Use for Hemostasis |
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