Characterization of different biodegradable scaffolds in tissue engineering
The aim of the present study was to compare the characteristics of acellular dermal matrix (ADM), small intestinal submucosa (SIS) and Bio‑Gide scaffolds with acellular vascular matrix (ACVM)‑0.25% human‑like collagen I (HLC‑I) scaffold in tissue engineering blood vessels. The ACVM‑0.25% HLC‑I scaff...
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Veröffentlicht in: | Molecular medicine reports 2019-05, Vol.19 (5), p.4043-4056 |
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creator | Qiu, Yan-Ling Chen, Xiao Hou, Ya-Li Hou, Yan-Juan Tian, Song-Bo Chen, Yu-He Yu, Li Nie, Min-Hai Liu, Xu-Qian |
description | The aim of the present study was to compare the characteristics of acellular dermal matrix (ADM), small intestinal submucosa (SIS) and Bio‑Gide scaffolds with acellular vascular matrix (ACVM)‑0.25% human‑like collagen I (HLC‑I) scaffold in tissue engineering blood vessels. The ACVM‑0.25% HLC‑I scaffold was prepared and compared with ADM, SIS and Bio‑Gide scaffolds via hematoxylin and eosin (H&E) staining, Masson staining and scanning electron microscope (SEM) observations. Primary human gingival fibroblasts (HGFs) were cultured and identified. Then, the experiment was established via the seeding of HGFs on different scaffolds for 1, 4 and 7 days. The compatibility of four different scaffolds with HGFs was evaluated by H&E staining, SEM observation and Cell Counting Kit‑8 assay. Then, a series of experiments were conducted to evaluate water absorption capacities, mechanical abilities, the ultra‑microstructure and the cytotoxicity of the four scaffolds. The ACVM‑0.25% HLC‑I scaffold was revealed to exhibit the best cell proliferation and good cell architecture. ADM and Bio‑Gide scaffolds exhibited good mechanical stability but cell proliferation was reduced when compared with the ACVM‑0.25% HLC‑I scaffold. In addition, SIS scaffolds exhibited the worst cell proliferation. The ACVM‑0.25% HLC‑I scaffold exhibited the best water absorption, followed by the SIS and Bio‑Gide scaffolds, and then the ADM scaffold. In conclusion, the ACVM‑0.25% HLC‑I scaffold has good mechanical properties as a tissue engineering scaffold and the present results suggest that it has better biological characterization when compared with other scaffold types. |
doi_str_mv | 10.3892/mmr.2019.10066 |
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The ACVM‑0.25% HLC‑I scaffold was prepared and compared with ADM, SIS and Bio‑Gide scaffolds via hematoxylin and eosin (H&E) staining, Masson staining and scanning electron microscope (SEM) observations. Primary human gingival fibroblasts (HGFs) were cultured and identified. Then, the experiment was established via the seeding of HGFs on different scaffolds for 1, 4 and 7 days. The compatibility of four different scaffolds with HGFs was evaluated by H&E staining, SEM observation and Cell Counting Kit‑8 assay. Then, a series of experiments were conducted to evaluate water absorption capacities, mechanical abilities, the ultra‑microstructure and the cytotoxicity of the four scaffolds. The ACVM‑0.25% HLC‑I scaffold was revealed to exhibit the best cell proliferation and good cell architecture. ADM and Bio‑Gide scaffolds exhibited good mechanical stability but cell proliferation was reduced when compared with the ACVM‑0.25% HLC‑I scaffold. In addition, SIS scaffolds exhibited the worst cell proliferation. The ACVM‑0.25% HLC‑I scaffold exhibited the best water absorption, followed by the SIS and Bio‑Gide scaffolds, and then the ADM scaffold. In conclusion, the ACVM‑0.25% HLC‑I scaffold has good mechanical properties as a tissue engineering scaffold and the present results suggest that it has better biological characterization when compared with other scaffold types.</description><identifier>ISSN: 1791-2997</identifier><identifier>EISSN: 1791-3004</identifier><identifier>DOI: 10.3892/mmr.2019.10066</identifier><identifier>PMID: 30896809</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Acids ; Biocompatibility ; Biodegradability ; Biomechanics ; Biomedical materials ; Blood vessels ; Cell adhesion & migration ; Cell growth ; Cell proliferation ; Collagen ; Collagen (type I) ; Composite materials ; Cytokines ; Cytotoxicity ; EDTA ; Electron microscopy ; Fibroblasts ; Intestine ; Mechanical properties ; Medical research ; Mucous membrane ; Polymers ; Rabbits ; Scanning electron microscopy ; Scanning microscopy ; Skin ; Smooth muscle ; Tissue engineering ; Water</subject><ispartof>Molecular medicine reports, 2019-05, Vol.19 (5), p.4043-4056</ispartof><rights>COPYRIGHT 2019 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2019</rights><rights>Copyright: © Qiu et al. 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-dad406b9da0d3e395326472afef5a1d051db493c0054e5082d45f5fb5e14d723</citedby><cites>FETCH-LOGICAL-c551t-dad406b9da0d3e395326472afef5a1d051db493c0054e5082d45f5fb5e14d723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30896809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qiu, Yan-Ling</creatorcontrib><creatorcontrib>Chen, Xiao</creatorcontrib><creatorcontrib>Hou, Ya-Li</creatorcontrib><creatorcontrib>Hou, Yan-Juan</creatorcontrib><creatorcontrib>Tian, Song-Bo</creatorcontrib><creatorcontrib>Chen, Yu-He</creatorcontrib><creatorcontrib>Yu, Li</creatorcontrib><creatorcontrib>Nie, Min-Hai</creatorcontrib><creatorcontrib>Liu, Xu-Qian</creatorcontrib><title>Characterization of different biodegradable scaffolds in tissue engineering</title><title>Molecular medicine reports</title><addtitle>Mol Med Rep</addtitle><description>The aim of the present study was to compare the characteristics of acellular dermal matrix (ADM), small intestinal submucosa (SIS) and Bio‑Gide scaffolds with acellular vascular matrix (ACVM)‑0.25% human‑like collagen I (HLC‑I) scaffold in tissue engineering blood vessels. The ACVM‑0.25% HLC‑I scaffold was prepared and compared with ADM, SIS and Bio‑Gide scaffolds via hematoxylin and eosin (H&E) staining, Masson staining and scanning electron microscope (SEM) observations. Primary human gingival fibroblasts (HGFs) were cultured and identified. Then, the experiment was established via the seeding of HGFs on different scaffolds for 1, 4 and 7 days. The compatibility of four different scaffolds with HGFs was evaluated by H&E staining, SEM observation and Cell Counting Kit‑8 assay. Then, a series of experiments were conducted to evaluate water absorption capacities, mechanical abilities, the ultra‑microstructure and the cytotoxicity of the four scaffolds. The ACVM‑0.25% HLC‑I scaffold was revealed to exhibit the best cell proliferation and good cell architecture. ADM and Bio‑Gide scaffolds exhibited good mechanical stability but cell proliferation was reduced when compared with the ACVM‑0.25% HLC‑I scaffold. In addition, SIS scaffolds exhibited the worst cell proliferation. The ACVM‑0.25% HLC‑I scaffold exhibited the best water absorption, followed by the SIS and Bio‑Gide scaffolds, and then the ADM scaffold. In conclusion, the ACVM‑0.25% HLC‑I scaffold has good mechanical properties as a tissue engineering scaffold and the present results suggest that it has better biological characterization when compared with other scaffold types.</description><subject>Acids</subject><subject>Biocompatibility</subject><subject>Biodegradability</subject><subject>Biomechanics</subject><subject>Biomedical materials</subject><subject>Blood vessels</subject><subject>Cell adhesion & migration</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Collagen</subject><subject>Collagen (type I)</subject><subject>Composite materials</subject><subject>Cytokines</subject><subject>Cytotoxicity</subject><subject>EDTA</subject><subject>Electron microscopy</subject><subject>Fibroblasts</subject><subject>Intestine</subject><subject>Mechanical properties</subject><subject>Medical research</subject><subject>Mucous membrane</subject><subject>Polymers</subject><subject>Rabbits</subject><subject>Scanning electron microscopy</subject><subject>Scanning microscopy</subject><subject>Skin</subject><subject>Smooth muscle</subject><subject>Tissue engineering</subject><subject>Water</subject><issn>1791-2997</issn><issn>1791-3004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptkUtv1TAQhS0EoqWwZYkisWFzL35NEm-QqisoiEpsurcce5y6SuxiJ0jw63HopTxUeWFr_J0zHh9CXjK6F73ib-c57zllas8obdtH5JR1iu0EpfLx8cyV6k7Is1JuKgEc1FNyImiv2p6qU_L5cG2ysQvm8MMsIcUm-cYF7zFjXJohJIdjNs4MEzbFGu_T5EoTYrOEUlZsMI4hYpXH8Tl54s1U8MVxPyNXH95fHT7uLr9cfDqcX-4sAFt2zjhJ20E5Q51AoUDwVnbcePRgmKPA3CCVsJSCRKA9dxI8-AGQSddxcUbe3dnersOMztZ3ZjPp2xxmk7_rZIL-9yaGaz2mb7p2YT3bDN4cDXL6umJZ9ByKxWkyEdNaNGcKeEdVBxV9_R96k9Yc63Sac8Z4X1n2hxrNhDpEn2pfu5nqc-hByh7ajdo_QNXlcA42RfSh1h8S2JxKyejvZ2RUb-nrmr7e0te_0q-CV3__zD3-O27xEzL8qsE</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Qiu, Yan-Ling</creator><creator>Chen, Xiao</creator><creator>Hou, Ya-Li</creator><creator>Hou, Yan-Juan</creator><creator>Tian, Song-Bo</creator><creator>Chen, Yu-He</creator><creator>Yu, Li</creator><creator>Nie, Min-Hai</creator><creator>Liu, Xu-Qian</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190501</creationdate><title>Characterization of different biodegradable scaffolds in tissue engineering</title><author>Qiu, Yan-Ling ; Chen, Xiao ; Hou, Ya-Li ; Hou, Yan-Juan ; Tian, Song-Bo ; Chen, Yu-He ; Yu, Li ; Nie, Min-Hai ; Liu, Xu-Qian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c551t-dad406b9da0d3e395326472afef5a1d051db493c0054e5082d45f5fb5e14d723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acids</topic><topic>Biocompatibility</topic><topic>Biodegradability</topic><topic>Biomechanics</topic><topic>Biomedical materials</topic><topic>Blood vessels</topic><topic>Cell adhesion & migration</topic><topic>Cell growth</topic><topic>Cell proliferation</topic><topic>Collagen</topic><topic>Collagen (type I)</topic><topic>Composite materials</topic><topic>Cytokines</topic><topic>Cytotoxicity</topic><topic>EDTA</topic><topic>Electron microscopy</topic><topic>Fibroblasts</topic><topic>Intestine</topic><topic>Mechanical properties</topic><topic>Medical research</topic><topic>Mucous membrane</topic><topic>Polymers</topic><topic>Rabbits</topic><topic>Scanning electron microscopy</topic><topic>Scanning microscopy</topic><topic>Skin</topic><topic>Smooth muscle</topic><topic>Tissue engineering</topic><topic>Water</topic><toplevel>online_resources</toplevel><creatorcontrib>Qiu, Yan-Ling</creatorcontrib><creatorcontrib>Chen, Xiao</creatorcontrib><creatorcontrib>Hou, Ya-Li</creatorcontrib><creatorcontrib>Hou, Yan-Juan</creatorcontrib><creatorcontrib>Tian, Song-Bo</creatorcontrib><creatorcontrib>Chen, Yu-He</creatorcontrib><creatorcontrib>Yu, Li</creatorcontrib><creatorcontrib>Nie, Min-Hai</creatorcontrib><creatorcontrib>Liu, Xu-Qian</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular medicine reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qiu, Yan-Ling</au><au>Chen, Xiao</au><au>Hou, Ya-Li</au><au>Hou, Yan-Juan</au><au>Tian, Song-Bo</au><au>Chen, Yu-He</au><au>Yu, Li</au><au>Nie, Min-Hai</au><au>Liu, Xu-Qian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of different biodegradable scaffolds in tissue engineering</atitle><jtitle>Molecular medicine reports</jtitle><addtitle>Mol Med Rep</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>19</volume><issue>5</issue><spage>4043</spage><epage>4056</epage><pages>4043-4056</pages><issn>1791-2997</issn><eissn>1791-3004</eissn><abstract>The aim of the present study was to compare the characteristics of acellular dermal matrix (ADM), small intestinal submucosa (SIS) and Bio‑Gide scaffolds with acellular vascular matrix (ACVM)‑0.25% human‑like collagen I (HLC‑I) scaffold in tissue engineering blood vessels. The ACVM‑0.25% HLC‑I scaffold was prepared and compared with ADM, SIS and Bio‑Gide scaffolds via hematoxylin and eosin (H&E) staining, Masson staining and scanning electron microscope (SEM) observations. Primary human gingival fibroblasts (HGFs) were cultured and identified. Then, the experiment was established via the seeding of HGFs on different scaffolds for 1, 4 and 7 days. The compatibility of four different scaffolds with HGFs was evaluated by H&E staining, SEM observation and Cell Counting Kit‑8 assay. Then, a series of experiments were conducted to evaluate water absorption capacities, mechanical abilities, the ultra‑microstructure and the cytotoxicity of the four scaffolds. The ACVM‑0.25% HLC‑I scaffold was revealed to exhibit the best cell proliferation and good cell architecture. ADM and Bio‑Gide scaffolds exhibited good mechanical stability but cell proliferation was reduced when compared with the ACVM‑0.25% HLC‑I scaffold. In addition, SIS scaffolds exhibited the worst cell proliferation. The ACVM‑0.25% HLC‑I scaffold exhibited the best water absorption, followed by the SIS and Bio‑Gide scaffolds, and then the ADM scaffold. In conclusion, the ACVM‑0.25% HLC‑I scaffold has good mechanical properties as a tissue engineering scaffold and the present results suggest that it has better biological characterization when compared with other scaffold types.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>30896809</pmid><doi>10.3892/mmr.2019.10066</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acids Biocompatibility Biodegradability Biomechanics Biomedical materials Blood vessels Cell adhesion & migration Cell growth Cell proliferation Collagen Collagen (type I) Composite materials Cytokines Cytotoxicity EDTA Electron microscopy Fibroblasts Intestine Mechanical properties Medical research Mucous membrane Polymers Rabbits Scanning electron microscopy Scanning microscopy Skin Smooth muscle Tissue engineering Water |
title | Characterization of different biodegradable scaffolds in tissue engineering |
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