{"title":"与牙基的粘附研究。5. 单体结构与附着力的关系[j]。","authors":"T Hayakawa, K Takahashi, M Tomari, K Horie","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The relationship between the structure of monomers with amide groups and their adhesiveness to tooth was investigated. The monomers used were methacrylamide (MA), p-methacryloxybenzamide (p-MBA), and 3,5-dimethacryloxybenzamide (3,5-DMBA). MA was commercially available. p-MBA and 3,5-DMBA were prepared from the reaction of methacryloyl chloride with p-hydroxybenzamide or 3,5-dihydroxybenzamide, respectively, in acetonitrile. The bovine enamel and dentin were etched with 10% citric acid -3% FeCl3 solution. The monomers were dissolved in MMA, and TBB-O was used as a polymerization initiator. The test samples were immersed in 37 degrees C water for 1 day, 1 month, or 3 months. Then the tensile bond strengths were measured. The bond strengths to enamel were almost the same, irrespective of the kinds of monomers after 1 day immersion. Although the bond strengths of MA (1.0%) and 3,5-DMBA (3.0%) decreased after 1 month immersion, those of MA (0.5%) and p-MBA (0.5%) did not decrease after 3 months immersion. There was no relationship between the bond strengths to enamel and the bending strengths of the resins. The bond strengths of 3,5-DMBA (1.0%) and 3,5-DMBA (3.0%) to dentin were about 5-7 MPa. The bond strengths of MA (0.5%) or MA (1.0%) decreased after 3 months or 1 month immersion, respectively. The bond strength of p-MBA (0.5%) did not decrease after 3 months immersion.</p>","PeriodicalId":77579,"journal":{"name":"Nichidai koku kagaku = Nihon University journal of oral science","volume":"15 3","pages":"328-37"},"PeriodicalIF":0.0000,"publicationDate":"1989-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Studies on adhesion to tooth substrate. 5. The relationship between the structure of monomers and their adhesiveness].\",\"authors\":\"T Hayakawa, K Takahashi, M Tomari, K Horie\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The relationship between the structure of monomers with amide groups and their adhesiveness to tooth was investigated. The monomers used were methacrylamide (MA), p-methacryloxybenzamide (p-MBA), and 3,5-dimethacryloxybenzamide (3,5-DMBA). MA was commercially available. p-MBA and 3,5-DMBA were prepared from the reaction of methacryloyl chloride with p-hydroxybenzamide or 3,5-dihydroxybenzamide, respectively, in acetonitrile. The bovine enamel and dentin were etched with 10% citric acid -3% FeCl3 solution. The monomers were dissolved in MMA, and TBB-O was used as a polymerization initiator. The test samples were immersed in 37 degrees C water for 1 day, 1 month, or 3 months. Then the tensile bond strengths were measured. The bond strengths to enamel were almost the same, irrespective of the kinds of monomers after 1 day immersion. Although the bond strengths of MA (1.0%) and 3,5-DMBA (3.0%) decreased after 1 month immersion, those of MA (0.5%) and p-MBA (0.5%) did not decrease after 3 months immersion. There was no relationship between the bond strengths to enamel and the bending strengths of the resins. The bond strengths of 3,5-DMBA (1.0%) and 3,5-DMBA (3.0%) to dentin were about 5-7 MPa. The bond strengths of MA (0.5%) or MA (1.0%) decreased after 3 months or 1 month immersion, respectively. The bond strength of p-MBA (0.5%) did not decrease after 3 months immersion.</p>\",\"PeriodicalId\":77579,\"journal\":{\"name\":\"Nichidai koku kagaku = Nihon University journal of oral science\",\"volume\":\"15 3\",\"pages\":\"328-37\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nichidai koku kagaku = Nihon University journal of oral science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nichidai koku kagaku = Nihon University journal of oral science","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Studies on adhesion to tooth substrate. 5. The relationship between the structure of monomers and their adhesiveness].
The relationship between the structure of monomers with amide groups and their adhesiveness to tooth was investigated. The monomers used were methacrylamide (MA), p-methacryloxybenzamide (p-MBA), and 3,5-dimethacryloxybenzamide (3,5-DMBA). MA was commercially available. p-MBA and 3,5-DMBA were prepared from the reaction of methacryloyl chloride with p-hydroxybenzamide or 3,5-dihydroxybenzamide, respectively, in acetonitrile. The bovine enamel and dentin were etched with 10% citric acid -3% FeCl3 solution. The monomers were dissolved in MMA, and TBB-O was used as a polymerization initiator. The test samples were immersed in 37 degrees C water for 1 day, 1 month, or 3 months. Then the tensile bond strengths were measured. The bond strengths to enamel were almost the same, irrespective of the kinds of monomers after 1 day immersion. Although the bond strengths of MA (1.0%) and 3,5-DMBA (3.0%) decreased after 1 month immersion, those of MA (0.5%) and p-MBA (0.5%) did not decrease after 3 months immersion. There was no relationship between the bond strengths to enamel and the bending strengths of the resins. The bond strengths of 3,5-DMBA (1.0%) and 3,5-DMBA (3.0%) to dentin were about 5-7 MPa. The bond strengths of MA (0.5%) or MA (1.0%) decreased after 3 months or 1 month immersion, respectively. The bond strength of p-MBA (0.5%) did not decrease after 3 months immersion.