4.6 Article

Effects of solvents on the early stage stiffening rate of demineralized dentin matrix

期刊

JOURNAL OF DENTISTRY
卷 33, 期 5, 页码 371-377

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jdent.2004.10.013

关键词

collagen; acetone; ethanol; methanol; propanol; HEMA; air; modulus of elasticity; stiffening rate

资金

  1. NIDCR NIH HHS [DE 014911] Funding Source: Medline

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Objectives. To monitor the stiffening rate of demineralized dentin matrix at the early stages after exposure to different neat solvents. Methods. Dentin beams approximately 0.8x0.7x8.0mm were obtained from human third molars. After covering their ends with resin composite, the middle exposed length of 4.0 mm (gauge-length) was demineralized in 0.5 M EDTA (pH 7.0) for 7 days. The specimens were gripped by a testing machine, pre-loaded to 10 g and cyclically stressed in tension to 5% strain, for 30 repeated cycles (total 20 min) at 0.6 mm/min white immersed in water (control). Then, water was replaced by either 100% acetone, methanol, ethanol, propanol, HEMA or air and the specimens subjected to the same cyclic protocol. The maximum apparent modulus of elasticity (E-Max) was calculated for every cycle, plotted as a function of time and subjected to regression analysis. Stiffening rate was calculated as changes in E (min). Regression analysis examined the relationship between E and time for each solvent. Data were analyzed by one-way ANOVA and Student-Newman-Keuls test at alpha=0.05. Results. Regression analysis showed that E increased significantly with time in all water-free solvents (R-2=0.8-0.99). Stiffening rate was higher for acetone (0.9MPa/min) and ethanol (0.8MPa/min), intermediate for air (0.7MPa/min), methanol (0.6MPa/min) and propanol (0.5 MPa/min), lower for HEMA (0.2 MPa/min) and practically none for water (0.07 MPa/min) with p < 0.05. Conclusions. The solvent-induced stiffening rate of demineralized dentin matrix is both time and solvent-dependent. The ability of solvents to promptly stiffen the demineralized dentin matrix may be important in maintaining the resin-infiltrated matrix expanded during the solvent evaporation stage of resin bonding. (c) 2004 Elsevier Ltd. AIL rights reserved.

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