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3D printed TCP-based scaffold incorporating VEGF-loaded PLGA microspheres for craniofacial tissue engineering
Vascularization is a critical process during bone regeneration/repair and the lack of tissue vascularization is recognized as a major challenge in applying bone tissue engineering methods for cranial and maxillofacial surgeries. The aim of our study is to fabricate a vascular endothelial growth fact...
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Published in: | Dental materials 2017-11, Vol.33 (11), p.1205-1216 |
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container_title | Dental materials |
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creator | Fahimipour, F. Rasoulianboroujeni, M. Dashtimoghadam, E. Khoshroo, K. Tahriri, M. Bastami, F. Lobner, D. Tayebi, L. |
description | Vascularization is a critical process during bone regeneration/repair and the lack of tissue vascularization is recognized as a major challenge in applying bone tissue engineering methods for cranial and maxillofacial surgeries. The aim of our study is to fabricate a vascular endothelial growth factor (VEGF)-loaded gelatin/alginate/β-TCP composite scaffold by 3D printing method using a computer-assisted design (CAD) model.
The paste, composed of (VEGF-loaded PLGA)-containing gelatin/alginate/β-TCP in water, was loaded into standard Nordson cartridges and promptly employed for printing the scaffolds. Rheological characterization of various gelatin/alginate/β-TCP formulations led to an optimized paste as a printable bioink at room temperature.
The in vitro release kinetics of the loaded VEGF revealed that the designed scaffolds fulfill the bioavailability of VEGF required for vascularization in the early stages of tissue regeneration. The results were confirmed by two times increment of proliferation of human umbilical vein endothelial cells (HUVECs) seeded on the scaffolds after 10 days. The compressive modulus of the scaffolds, 98±11MPa, was found to be in the range of cancellous bone suggesting their potential application for craniofacial tissue engineering. Osteoblast culture on the scaffolds showed that the construct supports cell viability, adhesion and proliferation. It was found that the ALP activity increased over 50% using VEGF-loaded scaffolds after 2 weeks of culture.
The 3D printed gelatin/alginate/β-TCP scaffold with slow releasing of VEGF can be considered as a potential candidate for regeneration of craniofacial defects. |
doi_str_mv | 10.1016/j.dental.2017.06.016 |
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The paste, composed of (VEGF-loaded PLGA)-containing gelatin/alginate/β-TCP in water, was loaded into standard Nordson cartridges and promptly employed for printing the scaffolds. Rheological characterization of various gelatin/alginate/β-TCP formulations led to an optimized paste as a printable bioink at room temperature.
The in vitro release kinetics of the loaded VEGF revealed that the designed scaffolds fulfill the bioavailability of VEGF required for vascularization in the early stages of tissue regeneration. The results were confirmed by two times increment of proliferation of human umbilical vein endothelial cells (HUVECs) seeded on the scaffolds after 10 days. The compressive modulus of the scaffolds, 98±11MPa, was found to be in the range of cancellous bone suggesting their potential application for craniofacial tissue engineering. Osteoblast culture on the scaffolds showed that the construct supports cell viability, adhesion and proliferation. It was found that the ALP activity increased over 50% using VEGF-loaded scaffolds after 2 weeks of culture.
The 3D printed gelatin/alginate/β-TCP scaffold with slow releasing of VEGF can be considered as a potential candidate for regeneration of craniofacial defects.</description><identifier>ISSN: 0109-5641</identifier><identifier>EISSN: 1879-0097</identifier><identifier>DOI: 10.1016/j.dental.2017.06.016</identifier><identifier>PMID: 28882369</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>3-D printers ; 3D printing ; Alginic acid ; Bioavailability ; Biocompatibility ; Biomedical materials ; Bone growth ; Calcium phosphates ; Cancellous bone ; Cartridges ; Cell culture ; Cell proliferation ; Defects ; Dentistry ; Endothelial cells ; Formulations ; Gelatin ; Kinetics ; Maxillofacial ; Microspheres ; Modulus of elasticity ; PLGA microsphere ; Polylactide-co-glycolide ; Printing ; Regeneration ; Regeneration (physiology) ; Rheological properties ; Scaffold ; Scaffolds ; Skull ; Three dimensional composites ; Three dimensional printing ; Tissue culture ; Tissue engineering ; Umbilical vein ; Vascular endothelial growth factor ; Vascularization ; VEGF ; β-Tricalcium phosphate</subject><ispartof>Dental materials, 2017-11, Vol.33 (11), p.1205-1216</ispartof><rights>2017 The Academy of Dental Materials</rights><rights>Copyright © 2017 The Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier BV Nov 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c608t-919dbd972cf64059ce9291845acfc9b5de7bbc733229ae5e2741541fe690af7a3</citedby><cites>FETCH-LOGICAL-c608t-919dbd972cf64059ce9291845acfc9b5de7bbc733229ae5e2741541fe690af7a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28882369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fahimipour, F.</creatorcontrib><creatorcontrib>Rasoulianboroujeni, M.</creatorcontrib><creatorcontrib>Dashtimoghadam, E.</creatorcontrib><creatorcontrib>Khoshroo, K.</creatorcontrib><creatorcontrib>Tahriri, M.</creatorcontrib><creatorcontrib>Bastami, F.</creatorcontrib><creatorcontrib>Lobner, D.</creatorcontrib><creatorcontrib>Tayebi, L.</creatorcontrib><title>3D printed TCP-based scaffold incorporating VEGF-loaded PLGA microspheres for craniofacial tissue engineering</title><title>Dental materials</title><addtitle>Dent Mater</addtitle><description>Vascularization is a critical process during bone regeneration/repair and the lack of tissue vascularization is recognized as a major challenge in applying bone tissue engineering methods for cranial and maxillofacial surgeries. The aim of our study is to fabricate a vascular endothelial growth factor (VEGF)-loaded gelatin/alginate/β-TCP composite scaffold by 3D printing method using a computer-assisted design (CAD) model.
The paste, composed of (VEGF-loaded PLGA)-containing gelatin/alginate/β-TCP in water, was loaded into standard Nordson cartridges and promptly employed for printing the scaffolds. Rheological characterization of various gelatin/alginate/β-TCP formulations led to an optimized paste as a printable bioink at room temperature.
The in vitro release kinetics of the loaded VEGF revealed that the designed scaffolds fulfill the bioavailability of VEGF required for vascularization in the early stages of tissue regeneration. The results were confirmed by two times increment of proliferation of human umbilical vein endothelial cells (HUVECs) seeded on the scaffolds after 10 days. The compressive modulus of the scaffolds, 98±11MPa, was found to be in the range of cancellous bone suggesting their potential application for craniofacial tissue engineering. Osteoblast culture on the scaffolds showed that the construct supports cell viability, adhesion and proliferation. It was found that the ALP activity increased over 50% using VEGF-loaded scaffolds after 2 weeks of culture.
The 3D printed gelatin/alginate/β-TCP scaffold with slow releasing of VEGF can be considered as a potential candidate for regeneration of craniofacial defects.</description><subject>3-D printers</subject><subject>3D printing</subject><subject>Alginic acid</subject><subject>Bioavailability</subject><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Bone growth</subject><subject>Calcium phosphates</subject><subject>Cancellous bone</subject><subject>Cartridges</subject><subject>Cell culture</subject><subject>Cell proliferation</subject><subject>Defects</subject><subject>Dentistry</subject><subject>Endothelial cells</subject><subject>Formulations</subject><subject>Gelatin</subject><subject>Kinetics</subject><subject>Maxillofacial</subject><subject>Microspheres</subject><subject>Modulus of elasticity</subject><subject>PLGA microsphere</subject><subject>Polylactide-co-glycolide</subject><subject>Printing</subject><subject>Regeneration</subject><subject>Regeneration (physiology)</subject><subject>Rheological properties</subject><subject>Scaffold</subject><subject>Scaffolds</subject><subject>Skull</subject><subject>Three dimensional composites</subject><subject>Three dimensional printing</subject><subject>Tissue culture</subject><subject>Tissue engineering</subject><subject>Umbilical vein</subject><subject>Vascular endothelial growth factor</subject><subject>Vascularization</subject><subject>VEGF</subject><subject>β-Tricalcium phosphate</subject><issn>0109-5641</issn><issn>1879-0097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9UU1v1DAQtRCIbgv_ACFLXLgk-COJ4wtStbQL0kr0ULhajj3eepXYi51U4t_j1bbl48DJ1sybefPeQ-gNJTUltPuwry2EWY81I1TUpKtL8Rla0V7IihApnqMVoURWbdfQM3Se854Q0jBJX6Iz1vc9451coYl_wofkwwwW365vqkHn8stGOxdHi30wMR1i0rMPO_z9anNdjVHbArnZbi7x5E2K-XAHCTJ2MWGTdPDRaeP1iGef8wIYws4HgEKye4VeOD1meP3wXqBv11e368_V9uvmy_pyW5mO9HMlqbSDlYIZ1zWklQZkubtvWm2ckUNrQQyDEZwzJjW0wERD24Y66CTRTmh-gT6e9h6WYQJrilFJj6oInXT6qaL26u9O8HdqF-9VRygvPGXB-4cFKf5YIM9q8tnAOOoAccmKSi5axqmgBfruH-g-LikUeQUlqGgI7XlBNSfU0bCcwD0dQ4k65qn26pSnOuapSKdKsYy9_VPI09BjgL-VQrHz3kNS2XgIBqxPYGZlo_8_wy-FLrSJ</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>Fahimipour, F.</creator><creator>Rasoulianboroujeni, M.</creator><creator>Dashtimoghadam, E.</creator><creator>Khoshroo, K.</creator><creator>Tahriri, M.</creator><creator>Bastami, F.</creator><creator>Lobner, D.</creator><creator>Tayebi, L.</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171101</creationdate><title>3D printed TCP-based scaffold incorporating VEGF-loaded PLGA microspheres for craniofacial tissue engineering</title><author>Fahimipour, F. ; Rasoulianboroujeni, M. ; Dashtimoghadam, E. ; Khoshroo, K. ; Tahriri, M. ; Bastami, F. ; Lobner, D. ; Tayebi, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c608t-919dbd972cf64059ce9291845acfc9b5de7bbc733229ae5e2741541fe690af7a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>3-D printers</topic><topic>3D printing</topic><topic>Alginic acid</topic><topic>Bioavailability</topic><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>Bone growth</topic><topic>Calcium phosphates</topic><topic>Cancellous bone</topic><topic>Cartridges</topic><topic>Cell culture</topic><topic>Cell proliferation</topic><topic>Defects</topic><topic>Dentistry</topic><topic>Endothelial cells</topic><topic>Formulations</topic><topic>Gelatin</topic><topic>Kinetics</topic><topic>Maxillofacial</topic><topic>Microspheres</topic><topic>Modulus of elasticity</topic><topic>PLGA microsphere</topic><topic>Polylactide-co-glycolide</topic><topic>Printing</topic><topic>Regeneration</topic><topic>Regeneration (physiology)</topic><topic>Rheological properties</topic><topic>Scaffold</topic><topic>Scaffolds</topic><topic>Skull</topic><topic>Three dimensional composites</topic><topic>Three dimensional printing</topic><topic>Tissue culture</topic><topic>Tissue engineering</topic><topic>Umbilical vein</topic><topic>Vascular endothelial growth factor</topic><topic>Vascularization</topic><topic>VEGF</topic><topic>β-Tricalcium phosphate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fahimipour, F.</creatorcontrib><creatorcontrib>Rasoulianboroujeni, M.</creatorcontrib><creatorcontrib>Dashtimoghadam, E.</creatorcontrib><creatorcontrib>Khoshroo, K.</creatorcontrib><creatorcontrib>Tahriri, M.</creatorcontrib><creatorcontrib>Bastami, F.</creatorcontrib><creatorcontrib>Lobner, D.</creatorcontrib><creatorcontrib>Tayebi, L.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</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>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Dental materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fahimipour, F.</au><au>Rasoulianboroujeni, M.</au><au>Dashtimoghadam, E.</au><au>Khoshroo, K.</au><au>Tahriri, M.</au><au>Bastami, F.</au><au>Lobner, D.</au><au>Tayebi, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>3D printed TCP-based scaffold incorporating VEGF-loaded PLGA microspheres for craniofacial tissue engineering</atitle><jtitle>Dental materials</jtitle><addtitle>Dent Mater</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>33</volume><issue>11</issue><spage>1205</spage><epage>1216</epage><pages>1205-1216</pages><issn>0109-5641</issn><eissn>1879-0097</eissn><abstract>Vascularization is a critical process during bone regeneration/repair and the lack of tissue vascularization is recognized as a major challenge in applying bone tissue engineering methods for cranial and maxillofacial surgeries. The aim of our study is to fabricate a vascular endothelial growth factor (VEGF)-loaded gelatin/alginate/β-TCP composite scaffold by 3D printing method using a computer-assisted design (CAD) model.
The paste, composed of (VEGF-loaded PLGA)-containing gelatin/alginate/β-TCP in water, was loaded into standard Nordson cartridges and promptly employed for printing the scaffolds. Rheological characterization of various gelatin/alginate/β-TCP formulations led to an optimized paste as a printable bioink at room temperature.
The in vitro release kinetics of the loaded VEGF revealed that the designed scaffolds fulfill the bioavailability of VEGF required for vascularization in the early stages of tissue regeneration. The results were confirmed by two times increment of proliferation of human umbilical vein endothelial cells (HUVECs) seeded on the scaffolds after 10 days. The compressive modulus of the scaffolds, 98±11MPa, was found to be in the range of cancellous bone suggesting their potential application for craniofacial tissue engineering. Osteoblast culture on the scaffolds showed that the construct supports cell viability, adhesion and proliferation. It was found that the ALP activity increased over 50% using VEGF-loaded scaffolds after 2 weeks of culture.
The 3D printed gelatin/alginate/β-TCP scaffold with slow releasing of VEGF can be considered as a potential candidate for regeneration of craniofacial defects.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28882369</pmid><doi>10.1016/j.dental.2017.06.016</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3-D printers 3D printing Alginic acid Bioavailability Biocompatibility Biomedical materials Bone growth Calcium phosphates Cancellous bone Cartridges Cell culture Cell proliferation Defects Dentistry Endothelial cells Formulations Gelatin Kinetics Maxillofacial Microspheres Modulus of elasticity PLGA microsphere Polylactide-co-glycolide Printing Regeneration Regeneration (physiology) Rheological properties Scaffold Scaffolds Skull Three dimensional composites Three dimensional printing Tissue culture Tissue engineering Umbilical vein Vascular endothelial growth factor Vascularization VEGF β-Tricalcium phosphate |
title | 3D printed TCP-based scaffold incorporating VEGF-loaded PLGA microspheres for craniofacial tissue engineering |
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