Synthesis and Characterization of a Chemico-structurally Modified Bis -GMA Analog for Dental Applications
This study aimed to synthesize and characterize a novel -GMA analog, termed P- -GMA, through structural modification by replacing hydroxyl (-OH) groups with phosphonooxy [-O-P(=O)(OH) ] groups and to evaluate and compare its viscosity with -GMA. -GMA, triethylamine, dichloromethane, and phosphoryl c...
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Veröffentlicht in: | The journal of contemporary dental practice 2024-06, Vol.25 (6), p.588-592 |
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container_title | The journal of contemporary dental practice |
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creator | Ajay, Ranganathan Selvabalaji, Arumugam Muthamilselvi, Mathi Vasanthakumari, Ananthan Sonia, Abraham Deepa, Gurunathan |
description | This study aimed to synthesize and characterize a novel
-GMA analog, termed P-
-GMA, through structural modification by replacing hydroxyl (-OH) groups with phosphonooxy [-O-P(=O)(OH)
] groups and to evaluate and compare its viscosity with
-GMA.
-GMA, triethylamine, dichloromethane, and phosphoryl chloride were utilized for the synthesis of P-
-GMA through phosphorylation. Fourier discerned the chemical structure of the synthesized P-
-GMA transform infrared spectroscopy (FTIR), and its viscosity was assessed by rheometry in oscillatory shear mode over a frequency sweep range of 0.1-100 (ω, rad/s) at 25°C with a 25 mm parallel plate design and a 0.5 mm gap. The data was recorded and statistically analyzed.
The FTIR analysis confirmed the successful synthesis of P-
-GMA, evidenced by the disappearance of hydroxyl (-OH) peaks and the emergence of phosphonooxy [-O-P(=O)(OH)
] peaks in the P-
-GMA. Rheological testing demonstrated a notable reduction in viscosity for P-
-GMA (436.62 Pa.s) when compared to conventional
-GMA (1089.02 Pa.s), indicating improved handling characteristics.
P-
-GMA was successfully synthesized by phosphorylation reaction where the -OH groups responsible for the high viscosity in the
-GMA were replaced with the [-O-P(=O)(OH)
] groups with significantly reduced viscosity.
The development of P-
-GMA holds promise for simplifying dental procedures by reducing chairside time with uncooperative children. The
-GMA-based composites possess self-adhering properties thereby eschewing the etching and bonding procedures with reduced moisture contamination of the restoration during bonding. This ultimately leads to better clinical outcomes and improved patient experiences by reducing technical vulnerabilities. How to cite this article: Ajay R, Selvabalaji A, Muthamilselvi M, et al. Synthesis and Characterization of a Chemico-structurally Modified Bis-GMA Analog for Dental Applications. J Contemp Dent Pract 2024;25(6):588-592. |
doi_str_mv | 10.5005/jp-journals-10024-3687 |
format | Article |
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-GMA analog, termed P-
-GMA, through structural modification by replacing hydroxyl (-OH) groups with phosphonooxy [-O-P(=O)(OH)
] groups and to evaluate and compare its viscosity with
-GMA.
-GMA, triethylamine, dichloromethane, and phosphoryl chloride were utilized for the synthesis of P-
-GMA through phosphorylation. Fourier discerned the chemical structure of the synthesized P-
-GMA transform infrared spectroscopy (FTIR), and its viscosity was assessed by rheometry in oscillatory shear mode over a frequency sweep range of 0.1-100 (ω, rad/s) at 25°C with a 25 mm parallel plate design and a 0.5 mm gap. The data was recorded and statistically analyzed.
The FTIR analysis confirmed the successful synthesis of P-
-GMA, evidenced by the disappearance of hydroxyl (-OH) peaks and the emergence of phosphonooxy [-O-P(=O)(OH)
] peaks in the P-
-GMA. Rheological testing demonstrated a notable reduction in viscosity for P-
-GMA (436.62 Pa.s) when compared to conventional
-GMA (1089.02 Pa.s), indicating improved handling characteristics.
P-
-GMA was successfully synthesized by phosphorylation reaction where the -OH groups responsible for the high viscosity in the
-GMA were replaced with the [-O-P(=O)(OH)
] groups with significantly reduced viscosity.
The development of P-
-GMA holds promise for simplifying dental procedures by reducing chairside time with uncooperative children. The
-GMA-based composites possess self-adhering properties thereby eschewing the etching and bonding procedures with reduced moisture contamination of the restoration during bonding. This ultimately leads to better clinical outcomes and improved patient experiences by reducing technical vulnerabilities. How to cite this article: Ajay R, Selvabalaji A, Muthamilselvi M, et al. Synthesis and Characterization of a Chemico-structurally Modified Bis-GMA Analog for Dental Applications. J Contemp Dent Pract 2024;25(6):588-592.</description><identifier>ISSN: 1526-3711</identifier><identifier>EISSN: 1526-3711</identifier><identifier>DOI: 10.5005/jp-journals-10024-3687</identifier><identifier>PMID: 39364826</identifier><language>eng</language><publisher>India</publisher><subject>Bisphenol A-Glycidyl Methacrylate - chemistry ; Dental Materials - chemical synthesis ; Dental Materials - chemistry ; Materials Testing ; Rheology ; Spectroscopy, Fourier Transform Infrared ; Viscosity</subject><ispartof>The journal of contemporary dental practice, 2024-06, Vol.25 (6), p.588-592</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1036-f19bfd2f48b954fda91f0a27a4c74a55ea36706c11bd9b0dc5db4c87e56b80063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39364826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ajay, Ranganathan</creatorcontrib><creatorcontrib>Selvabalaji, Arumugam</creatorcontrib><creatorcontrib>Muthamilselvi, Mathi</creatorcontrib><creatorcontrib>Vasanthakumari, Ananthan</creatorcontrib><creatorcontrib>Sonia, Abraham</creatorcontrib><creatorcontrib>Deepa, Gurunathan</creatorcontrib><title>Synthesis and Characterization of a Chemico-structurally Modified Bis -GMA Analog for Dental Applications</title><title>The journal of contemporary dental practice</title><addtitle>J Contemp Dent Pract</addtitle><description>This study aimed to synthesize and characterize a novel
-GMA analog, termed P-
-GMA, through structural modification by replacing hydroxyl (-OH) groups with phosphonooxy [-O-P(=O)(OH)
] groups and to evaluate and compare its viscosity with
-GMA.
-GMA, triethylamine, dichloromethane, and phosphoryl chloride were utilized for the synthesis of P-
-GMA through phosphorylation. Fourier discerned the chemical structure of the synthesized P-
-GMA transform infrared spectroscopy (FTIR), and its viscosity was assessed by rheometry in oscillatory shear mode over a frequency sweep range of 0.1-100 (ω, rad/s) at 25°C with a 25 mm parallel plate design and a 0.5 mm gap. The data was recorded and statistically analyzed.
The FTIR analysis confirmed the successful synthesis of P-
-GMA, evidenced by the disappearance of hydroxyl (-OH) peaks and the emergence of phosphonooxy [-O-P(=O)(OH)
] peaks in the P-
-GMA. Rheological testing demonstrated a notable reduction in viscosity for P-
-GMA (436.62 Pa.s) when compared to conventional
-GMA (1089.02 Pa.s), indicating improved handling characteristics.
P-
-GMA was successfully synthesized by phosphorylation reaction where the -OH groups responsible for the high viscosity in the
-GMA were replaced with the [-O-P(=O)(OH)
] groups with significantly reduced viscosity.
The development of P-
-GMA holds promise for simplifying dental procedures by reducing chairside time with uncooperative children. The
-GMA-based composites possess self-adhering properties thereby eschewing the etching and bonding procedures with reduced moisture contamination of the restoration during bonding. This ultimately leads to better clinical outcomes and improved patient experiences by reducing technical vulnerabilities. How to cite this article: Ajay R, Selvabalaji A, Muthamilselvi M, et al. Synthesis and Characterization of a Chemico-structurally Modified Bis-GMA Analog for Dental Applications. J Contemp Dent Pract 2024;25(6):588-592.</description><subject>Bisphenol A-Glycidyl Methacrylate - chemistry</subject><subject>Dental Materials - chemical synthesis</subject><subject>Dental Materials - chemistry</subject><subject>Materials Testing</subject><subject>Rheology</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><subject>Viscosity</subject><issn>1526-3711</issn><issn>1526-3711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtPwzAQhC0EoqXwFyofuRjsOHGSYyhQkFpxAM6W4wd1lMTBTg7l15O-EKddrWZmRx8Ac4LvEoyT-6pDlRt8K-qACMZRjCjL0jMwJUnEEE0JOf-3T8BVCNUoo1GKL8GE5pTFWcSmwL5v236jgw1QtAouNsIL2Wtvf0RvXQudgWK86sZKh0LvB9kPXtT1Fq6dssZqBR9GL1quC1iMbdwXNM7DR932ooZF19VW7pPCNbgwY1t9c5wz8Pn89LF4Qau35euiWCFJMGXIkLw0KjJxVuZJbJTIicEiSkUs01gkiRaUpZhJQkqVl1jJRJWxzFKdsDLDmNEZuD3kdt59Dzr0vLFB6roWrXZD4JSQKGM4T-koZQep9C4Erw3vvG2E33KC-Q4zrzp-wsz3mPkO82icH38MZaPVn-3Elf4Cb0N9Kw</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Ajay, Ranganathan</creator><creator>Selvabalaji, Arumugam</creator><creator>Muthamilselvi, Mathi</creator><creator>Vasanthakumari, Ananthan</creator><creator>Sonia, Abraham</creator><creator>Deepa, Gurunathan</creator><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>20240601</creationdate><title>Synthesis and Characterization of a Chemico-structurally Modified Bis -GMA Analog for Dental Applications</title><author>Ajay, Ranganathan ; Selvabalaji, Arumugam ; Muthamilselvi, Mathi ; Vasanthakumari, Ananthan ; Sonia, Abraham ; Deepa, Gurunathan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1036-f19bfd2f48b954fda91f0a27a4c74a55ea36706c11bd9b0dc5db4c87e56b80063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Bisphenol A-Glycidyl Methacrylate - chemistry</topic><topic>Dental Materials - chemical synthesis</topic><topic>Dental Materials - chemistry</topic><topic>Materials Testing</topic><topic>Rheology</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><topic>Viscosity</topic><toplevel>online_resources</toplevel><creatorcontrib>Ajay, Ranganathan</creatorcontrib><creatorcontrib>Selvabalaji, Arumugam</creatorcontrib><creatorcontrib>Muthamilselvi, Mathi</creatorcontrib><creatorcontrib>Vasanthakumari, Ananthan</creatorcontrib><creatorcontrib>Sonia, Abraham</creatorcontrib><creatorcontrib>Deepa, Gurunathan</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>The journal of contemporary dental practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ajay, Ranganathan</au><au>Selvabalaji, Arumugam</au><au>Muthamilselvi, Mathi</au><au>Vasanthakumari, Ananthan</au><au>Sonia, Abraham</au><au>Deepa, Gurunathan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of a Chemico-structurally Modified Bis -GMA Analog for Dental Applications</atitle><jtitle>The journal of contemporary dental practice</jtitle><addtitle>J Contemp Dent Pract</addtitle><date>2024-06-01</date><risdate>2024</risdate><volume>25</volume><issue>6</issue><spage>588</spage><epage>592</epage><pages>588-592</pages><issn>1526-3711</issn><eissn>1526-3711</eissn><abstract>This study aimed to synthesize and characterize a novel
-GMA analog, termed P-
-GMA, through structural modification by replacing hydroxyl (-OH) groups with phosphonooxy [-O-P(=O)(OH)
] groups and to evaluate and compare its viscosity with
-GMA.
-GMA, triethylamine, dichloromethane, and phosphoryl chloride were utilized for the synthesis of P-
-GMA through phosphorylation. Fourier discerned the chemical structure of the synthesized P-
-GMA transform infrared spectroscopy (FTIR), and its viscosity was assessed by rheometry in oscillatory shear mode over a frequency sweep range of 0.1-100 (ω, rad/s) at 25°C with a 25 mm parallel plate design and a 0.5 mm gap. The data was recorded and statistically analyzed.
The FTIR analysis confirmed the successful synthesis of P-
-GMA, evidenced by the disappearance of hydroxyl (-OH) peaks and the emergence of phosphonooxy [-O-P(=O)(OH)
] peaks in the P-
-GMA. Rheological testing demonstrated a notable reduction in viscosity for P-
-GMA (436.62 Pa.s) when compared to conventional
-GMA (1089.02 Pa.s), indicating improved handling characteristics.
P-
-GMA was successfully synthesized by phosphorylation reaction where the -OH groups responsible for the high viscosity in the
-GMA were replaced with the [-O-P(=O)(OH)
] groups with significantly reduced viscosity.
The development of P-
-GMA holds promise for simplifying dental procedures by reducing chairside time with uncooperative children. The
-GMA-based composites possess self-adhering properties thereby eschewing the etching and bonding procedures with reduced moisture contamination of the restoration during bonding. This ultimately leads to better clinical outcomes and improved patient experiences by reducing technical vulnerabilities. How to cite this article: Ajay R, Selvabalaji A, Muthamilselvi M, et al. Synthesis and Characterization of a Chemico-structurally Modified Bis-GMA Analog for Dental Applications. J Contemp Dent Pract 2024;25(6):588-592.</abstract><cop>India</cop><pmid>39364826</pmid><doi>10.5005/jp-journals-10024-3687</doi><tpages>5</tpages></addata></record> |
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subjects | Bisphenol A-Glycidyl Methacrylate - chemistry Dental Materials - chemical synthesis Dental Materials - chemistry Materials Testing Rheology Spectroscopy, Fourier Transform Infrared Viscosity |
title | Synthesis and Characterization of a Chemico-structurally Modified Bis -GMA Analog for Dental Applications |
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