Preparation, Characterization, and Properties of Chitosan‐Based Semi‐Interpenetrating Polymer Networks and Poly(2‐hydroxyethyl methacrylate) Structure
In this study, semi‐interpenetrating polymer networks (semi‐IPNs) based on chitosan and poly(2‐hydroxyethyl methacrylate) (CS/PHEMA) are successfully fabricated through free radical polymerization of HEMA in the presence of CS solution with potassium persulfate (KPS) as an initiator and triethylene...
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Veröffentlicht in: | Macromolecular chemistry and physics 2022-12, Vol.223 (24), p.n/a |
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description | In this study, semi‐interpenetrating polymer networks (semi‐IPNs) based on chitosan and poly(2‐hydroxyethyl methacrylate) (CS/PHEMA) are successfully fabricated through free radical polymerization of HEMA in the presence of CS solution with potassium persulfate (KPS) as an initiator and triethylene glycol dimethacrylate (TEGDMA) as a crosslinking agent, aiming to develop semi‐IPNs CS/PHEMA structure properties by different feed ratios of CS/HEMA and TEGDMA. The resulting semi‐IPNs CS/PHEMA structure shows the presence of the two polymeric components in the polymer structure. The crosslinking results in the morphological structure, high porosity and pore structure, as well as interconnected pores on the surface, indicating that a semi‐IPNs hydrogel structure formed after polymerization. Moreover, the degree of swelling is excellent in different media ranging from 140 to 220%. The semi‐IPNs CS/PHEMA samples exhibit highly enhanced mechanical strength with crosslinking and show features of brittle materials in the dry state and rubber‐like materials in the wet state. Compressive structure exhibits retaining after stress removal. The polymeric decomposition occurs, corresponding to linear CS and PHEMA networks. The degradation behavior of semi‐IPNs CS/PHEMA promotes enzymatic biodegradation under simulated physiological conditions. Therefore, these CS/PHEMA semi‐IPNs materials can be suitable for use as biodegradable polymers and engineering scaffold materials.
Semi‐IPNs chitosan and PHEMA (CS/PHEMA) structures are successfully fabricated through free radical polymerization. The semi‐IPNs CS/PHEMA samples perform remarkably well in degree of swelling in different media ranging from 140 to 220%, as well as mechanical properties. Their semi‐IPNs CS/PHEMA samples retain structure after compression tests. The semi‐IPNs CS/PHEMA samples have enzymatic biodegradation under simulated physiological conditions. |
doi_str_mv | 10.1002/macp.202200282 |
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Semi‐IPNs chitosan and PHEMA (CS/PHEMA) structures are successfully fabricated through free radical polymerization. The semi‐IPNs CS/PHEMA samples perform remarkably well in degree of swelling in different media ranging from 140 to 220%, as well as mechanical properties. Their semi‐IPNs CS/PHEMA samples retain structure after compression tests. The semi‐IPNs CS/PHEMA samples have enzymatic biodegradation under simulated physiological conditions.</description><identifier>ISSN: 1022-1352</identifier><identifier>EISSN: 1521-3935</identifier><identifier>DOI: 10.1002/macp.202200282</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Biodegradability ; biodegradable materials ; Biodegradation ; Brittle materials ; Chitosan ; Crosslinking ; Free radical polymerization ; Free radicals ; Glycol dimethacrylates ; Hydrogels ; Interpenetrating networks ; Networks ; PHEMA ; Polyhydroxyethyl methacrylate ; Polymerization ; Polymers ; Porosity ; porous structures ; Potassium persulfate ; semi‐IPNs ; Triethylene glycol dimethacrylate</subject><ispartof>Macromolecular chemistry and physics, 2022-12, Vol.223 (24), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3132-eb1d6fc949e0b4ba0f37795394ed871dfec88417b4a7b5141d4b97a1ed0f6d4b3</citedby><cites>FETCH-LOGICAL-c3132-eb1d6fc949e0b4ba0f37795394ed871dfec88417b4a7b5141d4b97a1ed0f6d4b3</cites><orcidid>0000-0001-8058-9596</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmacp.202200282$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmacp.202200282$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Than‐ardna, Bhumin</creatorcontrib><creatorcontrib>Tamura, Hiroshi</creatorcontrib><creatorcontrib>Furuike, Tetsuya</creatorcontrib><title>Preparation, Characterization, and Properties of Chitosan‐Based Semi‐Interpenetrating Polymer Networks and Poly(2‐hydroxyethyl methacrylate) Structure</title><title>Macromolecular chemistry and physics</title><description>In this study, semi‐interpenetrating polymer networks (semi‐IPNs) based on chitosan and poly(2‐hydroxyethyl methacrylate) (CS/PHEMA) are successfully fabricated through free radical polymerization of HEMA in the presence of CS solution with potassium persulfate (KPS) as an initiator and triethylene glycol dimethacrylate (TEGDMA) as a crosslinking agent, aiming to develop semi‐IPNs CS/PHEMA structure properties by different feed ratios of CS/HEMA and TEGDMA. The resulting semi‐IPNs CS/PHEMA structure shows the presence of the two polymeric components in the polymer structure. The crosslinking results in the morphological structure, high porosity and pore structure, as well as interconnected pores on the surface, indicating that a semi‐IPNs hydrogel structure formed after polymerization. Moreover, the degree of swelling is excellent in different media ranging from 140 to 220%. The semi‐IPNs CS/PHEMA samples exhibit highly enhanced mechanical strength with crosslinking and show features of brittle materials in the dry state and rubber‐like materials in the wet state. Compressive structure exhibits retaining after stress removal. The polymeric decomposition occurs, corresponding to linear CS and PHEMA networks. The degradation behavior of semi‐IPNs CS/PHEMA promotes enzymatic biodegradation under simulated physiological conditions. Therefore, these CS/PHEMA semi‐IPNs materials can be suitable for use as biodegradable polymers and engineering scaffold materials.
Semi‐IPNs chitosan and PHEMA (CS/PHEMA) structures are successfully fabricated through free radical polymerization. The semi‐IPNs CS/PHEMA samples perform remarkably well in degree of swelling in different media ranging from 140 to 220%, as well as mechanical properties. Their semi‐IPNs CS/PHEMA samples retain structure after compression tests. The semi‐IPNs CS/PHEMA samples have enzymatic biodegradation under simulated physiological conditions.</description><subject>Biodegradability</subject><subject>biodegradable materials</subject><subject>Biodegradation</subject><subject>Brittle materials</subject><subject>Chitosan</subject><subject>Crosslinking</subject><subject>Free radical polymerization</subject><subject>Free radicals</subject><subject>Glycol dimethacrylates</subject><subject>Hydrogels</subject><subject>Interpenetrating networks</subject><subject>Networks</subject><subject>PHEMA</subject><subject>Polyhydroxyethyl methacrylate</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Porosity</subject><subject>porous structures</subject><subject>Potassium persulfate</subject><subject>semi‐IPNs</subject><subject>Triethylene glycol dimethacrylate</subject><issn>1022-1352</issn><issn>1521-3935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFUTtOw0AUtBBIhEBLbYkGJBx21_8yWHwiBbAUqK21_UwcbK95u1YwFUfgAJyOk7CRIyipZt5oZl4xhnFMyYQSwi5qnrUTRhjTR8B2jBF1GbXs0HZ3Nde6RW2X7RsHUq4IIQEJ_ZHxFSO0HLkqRXNuRktNMwVYvm8V3uRmjKIFVCVIUxTaUyohefP98XnJJeTmAupSH7NG51poQG3ammczFlVfA5r3oNYCX-TQpcVTpu3LPkfx1oNa9pVZa-AZ9hVXcGYuFHaZ6hAOjb2CVxKOtjg2nq6vHqNba_5wM4umcyuzqc0sSGnuFVnohEBSJ-WksH0_dO3QgTzwaV5AFgQO9VOH-6lLHZo7aehzCjkpPM3tsXEy9LYoXjuQKlmJDhv9MmG-63quQ71AuyaDK0MhJUKRtFjWHPuEkmSzQLJZIPldQAfCIbAuK-j_cSd30yj-y_4ALOCRkA</recordid><startdate>202212</startdate><enddate>202212</enddate><creator>Than‐ardna, Bhumin</creator><creator>Tamura, Hiroshi</creator><creator>Furuike, Tetsuya</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-8058-9596</orcidid></search><sort><creationdate>202212</creationdate><title>Preparation, Characterization, and Properties of Chitosan‐Based Semi‐Interpenetrating Polymer Networks and Poly(2‐hydroxyethyl methacrylate) Structure</title><author>Than‐ardna, Bhumin ; Tamura, Hiroshi ; Furuike, Tetsuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3132-eb1d6fc949e0b4ba0f37795394ed871dfec88417b4a7b5141d4b97a1ed0f6d4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biodegradability</topic><topic>biodegradable materials</topic><topic>Biodegradation</topic><topic>Brittle materials</topic><topic>Chitosan</topic><topic>Crosslinking</topic><topic>Free radical polymerization</topic><topic>Free radicals</topic><topic>Glycol dimethacrylates</topic><topic>Hydrogels</topic><topic>Interpenetrating networks</topic><topic>Networks</topic><topic>PHEMA</topic><topic>Polyhydroxyethyl methacrylate</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Porosity</topic><topic>porous structures</topic><topic>Potassium persulfate</topic><topic>semi‐IPNs</topic><topic>Triethylene glycol dimethacrylate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Than‐ardna, Bhumin</creatorcontrib><creatorcontrib>Tamura, Hiroshi</creatorcontrib><creatorcontrib>Furuike, Tetsuya</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Macromolecular chemistry and physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Than‐ardna, Bhumin</au><au>Tamura, Hiroshi</au><au>Furuike, Tetsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation, Characterization, and Properties of Chitosan‐Based Semi‐Interpenetrating Polymer Networks and Poly(2‐hydroxyethyl methacrylate) Structure</atitle><jtitle>Macromolecular chemistry and physics</jtitle><date>2022-12</date><risdate>2022</risdate><volume>223</volume><issue>24</issue><epage>n/a</epage><issn>1022-1352</issn><eissn>1521-3935</eissn><abstract>In this study, semi‐interpenetrating polymer networks (semi‐IPNs) based on chitosan and poly(2‐hydroxyethyl methacrylate) (CS/PHEMA) are successfully fabricated through free radical polymerization of HEMA in the presence of CS solution with potassium persulfate (KPS) as an initiator and triethylene glycol dimethacrylate (TEGDMA) as a crosslinking agent, aiming to develop semi‐IPNs CS/PHEMA structure properties by different feed ratios of CS/HEMA and TEGDMA. The resulting semi‐IPNs CS/PHEMA structure shows the presence of the two polymeric components in the polymer structure. The crosslinking results in the morphological structure, high porosity and pore structure, as well as interconnected pores on the surface, indicating that a semi‐IPNs hydrogel structure formed after polymerization. Moreover, the degree of swelling is excellent in different media ranging from 140 to 220%. The semi‐IPNs CS/PHEMA samples exhibit highly enhanced mechanical strength with crosslinking and show features of brittle materials in the dry state and rubber‐like materials in the wet state. Compressive structure exhibits retaining after stress removal. The polymeric decomposition occurs, corresponding to linear CS and PHEMA networks. The degradation behavior of semi‐IPNs CS/PHEMA promotes enzymatic biodegradation under simulated physiological conditions. Therefore, these CS/PHEMA semi‐IPNs materials can be suitable for use as biodegradable polymers and engineering scaffold materials.
Semi‐IPNs chitosan and PHEMA (CS/PHEMA) structures are successfully fabricated through free radical polymerization. The semi‐IPNs CS/PHEMA samples perform remarkably well in degree of swelling in different media ranging from 140 to 220%, as well as mechanical properties. Their semi‐IPNs CS/PHEMA samples retain structure after compression tests. The semi‐IPNs CS/PHEMA samples have enzymatic biodegradation under simulated physiological conditions.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/macp.202200282</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8058-9596</orcidid></addata></record> |
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subjects | Biodegradability biodegradable materials Biodegradation Brittle materials Chitosan Crosslinking Free radical polymerization Free radicals Glycol dimethacrylates Hydrogels Interpenetrating networks Networks PHEMA Polyhydroxyethyl methacrylate Polymerization Polymers Porosity porous structures Potassium persulfate semi‐IPNs Triethylene glycol dimethacrylate |
title | Preparation, Characterization, and Properties of Chitosan‐Based Semi‐Interpenetrating Polymer Networks and Poly(2‐hydroxyethyl methacrylate) Structure |
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