Amino acid surface modified bioglass: A candidate biomaterial for bone tissue engineering
Bioglasses are solid materials consisted of sodium oxide, calcium oxide, silicon dioxide and phosphorus in various proportions and have used in bone tissue engineering. There have been ongoing efforts to improve the surface properties of bioglasses to increase biocompatibility and performance. The a...
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description | Bioglasses are solid materials consisted of sodium oxide, calcium oxide, silicon dioxide and phosphorus in various proportions and have used in bone tissue engineering. There have been ongoing efforts to improve the surface properties of bioglasses to increase biocompatibility and performance. The aim of the present study is to modify the bioglass surface with an amino acid mixture consisting of arginine, aspartic acid, phenylalanine, cysteine, histidine and lysine, to characterize the surface, and to evaluate the performance and biocompatibility in vitro and in vivo. The untreated bioglass, bioglass kept in simulated body fluid (SBF), and modified bioglass were used in further evaluation. After confirmation of the surface modification with FT‐IR analyses and SEM analyses, MC3T3‐E1 preosteoblasts adhesion on the surface was also revealed by SEM. The modified bioglass had significantly higher ALP activity in colorimetric measurement, rate of calcium accumulations in Alizarin red s staining, lower rate of cell death in Annexin‐V/PI staining to determine apoptosis and necrosis. Having higher cell viability rate in MTT test and absence of genotoxicity in micronucleus test (OECD 487), the modified bioglass was further confirmed for biocompatibility in vitro. The results of the rat tibial defect model revealed that the all bioglass treatments had a significantly better bone healing score compared to the untreated negative control. However, the modified bioglass exhibited significantly better bone healing efforts especially during the first and the second months compared to the other bioglass treatment treatments. As a result, the amino acid surface modification of bioglasses improves the surface biocompatibility and osteogenic performance that makes the amino acid modified bioglass a better candidate for bone tissue engineering.Research HighlightsBioglass surface modification with amino acids contributes to bioglass‐tissue interaction with an improved cell attachment.Modified bioglass increases in vitro Alp activity and calcium accumulation, and also positively affects cell behavior by supporting cell adaptation.Bioglass exerts osteogenic potential in vivo especially during early bone healing. |
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There have been ongoing efforts to improve the surface properties of bioglasses to increase biocompatibility and performance. The aim of the present study is to modify the bioglass surface with an amino acid mixture consisting of arginine, aspartic acid, phenylalanine, cysteine, histidine and lysine, to characterize the surface, and to evaluate the performance and biocompatibility in vitro and in vivo. The untreated bioglass, bioglass kept in simulated body fluid (SBF), and modified bioglass were used in further evaluation. After confirmation of the surface modification with FT‐IR analyses and SEM analyses, MC3T3‐E1 preosteoblasts adhesion on the surface was also revealed by SEM. The modified bioglass had significantly higher ALP activity in colorimetric measurement, rate of calcium accumulations in Alizarin red s staining, lower rate of cell death in Annexin‐V/PI staining to determine apoptosis and necrosis. Having higher cell viability rate in MTT test and absence of genotoxicity in micronucleus test (OECD 487), the modified bioglass was further confirmed for biocompatibility in vitro. The results of the rat tibial defect model revealed that the all bioglass treatments had a significantly better bone healing score compared to the untreated negative control. However, the modified bioglass exhibited significantly better bone healing efforts especially during the first and the second months compared to the other bioglass treatment treatments. As a result, the amino acid surface modification of bioglasses improves the surface biocompatibility and osteogenic performance that makes the amino acid modified bioglass a better candidate for bone tissue engineering.Research HighlightsBioglass surface modification with amino acids contributes to bioglass‐tissue interaction with an improved cell attachment.Modified bioglass increases in vitro Alp activity and calcium accumulation, and also positively affects cell behavior by supporting cell adaptation.Bioglass exerts osteogenic potential in vivo especially during early bone healing.</description><identifier>ISSN: 1059-910X</identifier><identifier>EISSN: 1097-0029</identifier><identifier>DOI: 10.1002/jemt.24659</identifier><identifier>PMID: 39154380</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc</publisher><subject>Alizarin ; Amino acids ; Apoptosis ; Aspartic acid ; Bioaccumulation ; Biocompatibility ; Bioglass ; Biomaterials ; Biomedical materials ; Body fluids ; Bone biomaterials ; Bone healing ; Bones ; Calcium ; Calcium oxide ; Cell adhesion ; Cell death ; Cell viability ; Colorimetry ; Genotoxicity ; Healing ; Histidine ; In vitro methods and tests ; In vivo methods and tests ; Lime ; Lysine ; Necrosis ; Performance evaluation ; Phenylalanine ; Silicon dioxide ; Staining ; Surface properties ; Tissue engineering</subject><ispartof>Microscopy research and technique, 2025-01, Vol.88 (1), p.26-41</ispartof><rights>2024. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 The Author(s). published by Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27922,27923</link.rule.ids></links><search><creatorcontrib>Yasin Özkabadayı</creatorcontrib><creatorcontrib>Türk, Mustafa</creatorcontrib><creatorcontrib>Kumandaş, Ali</creatorcontrib><creatorcontrib>Karahan, Siyami</creatorcontrib><title>Amino acid surface modified bioglass: A candidate biomaterial for bone tissue engineering</title><title>Microscopy research and technique</title><description>Bioglasses are solid materials consisted of sodium oxide, calcium oxide, silicon dioxide and phosphorus in various proportions and have used in bone tissue engineering. There have been ongoing efforts to improve the surface properties of bioglasses to increase biocompatibility and performance. The aim of the present study is to modify the bioglass surface with an amino acid mixture consisting of arginine, aspartic acid, phenylalanine, cysteine, histidine and lysine, to characterize the surface, and to evaluate the performance and biocompatibility in vitro and in vivo. The untreated bioglass, bioglass kept in simulated body fluid (SBF), and modified bioglass were used in further evaluation. After confirmation of the surface modification with FT‐IR analyses and SEM analyses, MC3T3‐E1 preosteoblasts adhesion on the surface was also revealed by SEM. The modified bioglass had significantly higher ALP activity in colorimetric measurement, rate of calcium accumulations in Alizarin red s staining, lower rate of cell death in Annexin‐V/PI staining to determine apoptosis and necrosis. Having higher cell viability rate in MTT test and absence of genotoxicity in micronucleus test (OECD 487), the modified bioglass was further confirmed for biocompatibility in vitro. The results of the rat tibial defect model revealed that the all bioglass treatments had a significantly better bone healing score compared to the untreated negative control. However, the modified bioglass exhibited significantly better bone healing efforts especially during the first and the second months compared to the other bioglass treatment treatments. As a result, the amino acid surface modification of bioglasses improves the surface biocompatibility and osteogenic performance that makes the amino acid modified bioglass a better candidate for bone tissue engineering.Research HighlightsBioglass surface modification with amino acids contributes to bioglass‐tissue interaction with an improved cell attachment.Modified bioglass increases in vitro Alp activity and calcium accumulation, and also positively affects cell behavior by supporting cell adaptation.Bioglass exerts osteogenic potential in vivo especially during early bone healing.</description><subject>Alizarin</subject><subject>Amino acids</subject><subject>Apoptosis</subject><subject>Aspartic acid</subject><subject>Bioaccumulation</subject><subject>Biocompatibility</subject><subject>Bioglass</subject><subject>Biomaterials</subject><subject>Biomedical materials</subject><subject>Body fluids</subject><subject>Bone biomaterials</subject><subject>Bone healing</subject><subject>Bones</subject><subject>Calcium</subject><subject>Calcium oxide</subject><subject>Cell adhesion</subject><subject>Cell death</subject><subject>Cell viability</subject><subject>Colorimetry</subject><subject>Genotoxicity</subject><subject>Healing</subject><subject>Histidine</subject><subject>In vitro methods and tests</subject><subject>In vivo methods and tests</subject><subject>Lime</subject><subject>Lysine</subject><subject>Necrosis</subject><subject>Performance evaluation</subject><subject>Phenylalanine</subject><subject>Silicon dioxide</subject><subject>Staining</subject><subject>Surface properties</subject><subject>Tissue engineering</subject><issn>1059-910X</issn><issn>1097-0029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><recordid>eNpVjs9LwzAYhoMoTqcX_4KA587va9Iu8SJj-AsGXnbQU0mTtGa0yUxawf_eDnfx9L68Dzy8hNwgLBAgv9vZfljkvCzkCblAkMtsWuXpoRcykwjvM3KZ0g4AsUB-TmZMYsGZgAvyseqdD1RpZ2gaY6O0pX0wrnHW0NqFtlMp3dMV1cobZ9RgD2s_ZXSqo02ItA7e0sGlNFpqfeu8nZhvr8hZo7pkr485J9unx-36Jdu8Pb-uV5tsLzhkZVNqyYQtcGmWaIwREgUKoWvgwLmaQM0g59NbhVbVda0saCl0mStmIWdz8vCn3Y91b422foiqq_bR9Sr-VEG56j_x7rNqw3eFWBa5QJgMt0dDDF-jTUO1C2P00-eKIS8kAy6A_QJ0umyO</recordid><startdate>20250101</startdate><enddate>20250101</enddate><creator>Yasin Özkabadayı</creator><creator>Türk, Mustafa</creator><creator>Kumandaş, Ali</creator><creator>Karahan, Siyami</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley & Sons, Inc</general><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>7SS</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</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>RC3</scope><scope>5PM</scope></search><sort><creationdate>20250101</creationdate><title>Amino acid surface modified bioglass: A candidate biomaterial for bone tissue engineering</title><author>Yasin Özkabadayı ; Türk, Mustafa ; Kumandaş, Ali ; Karahan, Siyami</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p840-6f6c938e517d71ddd8918188cb04044ae51b3024438a1eabbbae0c98c62a3e023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Alizarin</topic><topic>Amino acids</topic><topic>Apoptosis</topic><topic>Aspartic acid</topic><topic>Bioaccumulation</topic><topic>Biocompatibility</topic><topic>Bioglass</topic><topic>Biomaterials</topic><topic>Biomedical materials</topic><topic>Body fluids</topic><topic>Bone biomaterials</topic><topic>Bone healing</topic><topic>Bones</topic><topic>Calcium</topic><topic>Calcium oxide</topic><topic>Cell adhesion</topic><topic>Cell death</topic><topic>Cell viability</topic><topic>Colorimetry</topic><topic>Genotoxicity</topic><topic>Healing</topic><topic>Histidine</topic><topic>In vitro methods and tests</topic><topic>In vivo methods and tests</topic><topic>Lime</topic><topic>Lysine</topic><topic>Necrosis</topic><topic>Performance evaluation</topic><topic>Phenylalanine</topic><topic>Silicon dioxide</topic><topic>Staining</topic><topic>Surface properties</topic><topic>Tissue engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yasin Özkabadayı</creatorcontrib><creatorcontrib>Türk, Mustafa</creatorcontrib><creatorcontrib>Kumandaş, Ali</creatorcontrib><creatorcontrib>Karahan, Siyami</creatorcontrib><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>Entomology Abstracts (Full archive)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</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>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Microscopy research and technique</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yasin Özkabadayı</au><au>Türk, Mustafa</au><au>Kumandaş, Ali</au><au>Karahan, Siyami</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amino acid surface modified bioglass: A candidate biomaterial for bone tissue engineering</atitle><jtitle>Microscopy research and technique</jtitle><date>2025-01-01</date><risdate>2025</risdate><volume>88</volume><issue>1</issue><spage>26</spage><epage>41</epage><pages>26-41</pages><issn>1059-910X</issn><eissn>1097-0029</eissn><abstract>Bioglasses are solid materials consisted of sodium oxide, calcium oxide, silicon dioxide and phosphorus in various proportions and have used in bone tissue engineering. There have been ongoing efforts to improve the surface properties of bioglasses to increase biocompatibility and performance. The aim of the present study is to modify the bioglass surface with an amino acid mixture consisting of arginine, aspartic acid, phenylalanine, cysteine, histidine and lysine, to characterize the surface, and to evaluate the performance and biocompatibility in vitro and in vivo. The untreated bioglass, bioglass kept in simulated body fluid (SBF), and modified bioglass were used in further evaluation. After confirmation of the surface modification with FT‐IR analyses and SEM analyses, MC3T3‐E1 preosteoblasts adhesion on the surface was also revealed by SEM. The modified bioglass had significantly higher ALP activity in colorimetric measurement, rate of calcium accumulations in Alizarin red s staining, lower rate of cell death in Annexin‐V/PI staining to determine apoptosis and necrosis. Having higher cell viability rate in MTT test and absence of genotoxicity in micronucleus test (OECD 487), the modified bioglass was further confirmed for biocompatibility in vitro. The results of the rat tibial defect model revealed that the all bioglass treatments had a significantly better bone healing score compared to the untreated negative control. However, the modified bioglass exhibited significantly better bone healing efforts especially during the first and the second months compared to the other bioglass treatment treatments. As a result, the amino acid surface modification of bioglasses improves the surface biocompatibility and osteogenic performance that makes the amino acid modified bioglass a better candidate for bone tissue engineering.Research HighlightsBioglass surface modification with amino acids contributes to bioglass‐tissue interaction with an improved cell attachment.Modified bioglass increases in vitro Alp activity and calcium accumulation, and also positively affects cell behavior by supporting cell adaptation.Bioglass exerts osteogenic potential in vivo especially during early bone healing.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc</pub><pmid>39154380</pmid><doi>10.1002/jemt.24659</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alizarin Amino acids Apoptosis Aspartic acid Bioaccumulation Biocompatibility Bioglass Biomaterials Biomedical materials Body fluids Bone biomaterials Bone healing Bones Calcium Calcium oxide Cell adhesion Cell death Cell viability Colorimetry Genotoxicity Healing Histidine In vitro methods and tests In vivo methods and tests Lime Lysine Necrosis Performance evaluation Phenylalanine Silicon dioxide Staining Surface properties Tissue engineering |
title | Amino acid surface modified bioglass: A candidate biomaterial for bone tissue engineering |
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