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Polymerization shrinkage kinetics of silorane-based composites
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Basic Research Polymerization shrinkage kinetics of silorane-based composites
Youngchul Kwon, In-Bog Lee
Journal of Korean Academy of Conservative Dentistry 2010;35(1):51-58.
DOI: https://doi.org/10.5395/JKACD.2010.35.1.051
Published online: January 31, 2010

Department of Conservative Dentistry, School of Dentistry, Seoul National University, Korea.

Corresponding Author: In-Bog Lee. Department of Conservative Dentistry & Dental Research Institute, School of Dentistry, Seoul National University, 275-1 Yoengeon-Dong, Jongno-Gu, Seoul 110-786, Korea. Tel: 82-2-2072-3953, Fax: 82-2-2072-3859, inboglee@snu.ac.kr
• Received: January 10, 2010   • Revised: January 13, 2010   • Accepted: January 14, 2010

Copyright © 2010 Korean Academy of Conservative Dentistry

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  • Dental composites have improved significantly in physical properties over the past few decades. However, polymerization shrinkage and stress is still the major drawback of composites, limiting its use to selected cases. Much effort has been made to make low shrinking composites to overcome this issue and silorane-based composites have recently been introduced into the market.
    The aim of this study was to measure the volumetric polymerization shrinkage kinetics of a silorane-based composite and compare it with conventional methacrylate-based composites in order to evaluate its effectiveness in reducing polymerization shrinkage.
    Five commercial methacrylate-based (Beautifil, Z100, Z250, Z350 and Gradia X) and a silorane-based (P90) composites were investigated. The volumetric change of the composites during light polymerization was detected continuously as buoyancy change in distilled water by means of Archemedes'principle, using a newly made volume shrinkage measurement instrument. The null hypothesis was that there were no differences in polymerization shrinkage, peak polymerization shrinkage rate and peak shrinkage time between the silorane-based composite and methacrylate-based composites. The results were as follows:
    1. The shrinkage of silorane-based (P90) composites was the lowest (1.48%), and that of Beautifil composite was the highest (2.80%). There were also significant differences between brands among the methacrylate-based composites.

    2. Peak polymerization shrinkage rate was the lowest in P90 (0.13%/s) and the highest in Z100 (0.34%/s).

    3. The time to reach peak shrinkage rate of the silorane-based composite (P90) was longer (6.7 s) than those of the methacrylate-based composites (2.4-3.1 s).

    4. Peak shrinkage rate showed a strong positive correlation with the product of polymerization shrinkage and the inverse of peak shrinkage time (R = 0.95).

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Figure 1
Schematic diagram of the instrument for measuring polymerization shrinkage.
jkacd-35-51-g001.jpg
Figure 2
(a) Representative curves of polymerization shrinkage (%) and (b) Polymerization shrinkage rate (%/s) of composites as a function of time.
jkacd-35-51-g002.jpg
Figure 3
(a) Polymerization shrinkage (%), (b) Peak shrinkage rate (%/s), and (c) Peak shrinkage time (s) of composites.
jkacd-35-51-g003.jpg
Table 1
Composites used in this study
jkacd-35-51-i001.jpg
Table 2
Polymerization shrinkage (%) at 10 min, peak shrinkage rate (%/s), peak shrinkage time (s), and the inverse of peak shrinkage time (1/s) of composites

Mean values with the same superscripts are not significantly different (p > 0.05).

Number in parenthesis is standard deviation.

jkacd-35-51-i002.jpg
Table 3
Correlation analysis among polymerization shrinkage (%), peak shrinkage rate (%/s), peak shrinkage time (s), the inverse of peak time (1/s), and the product of polymerization shrinkage and the inverse of peak time of the composites
jkacd-35-51-i003.jpg

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        Polymerization shrinkage kinetics of silorane-based composites
        J Korean Acad Conserv Dent. 2010;35(1):51-58.   Published online January 31, 2010
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      Polymerization shrinkage kinetics of silorane-based composites
      Image Image Image
      Figure 1 Schematic diagram of the instrument for measuring polymerization shrinkage.
      Figure 2 (a) Representative curves of polymerization shrinkage (%) and (b) Polymerization shrinkage rate (%/s) of composites as a function of time.
      Figure 3 (a) Polymerization shrinkage (%), (b) Peak shrinkage rate (%/s), and (c) Peak shrinkage time (s) of composites.
      Polymerization shrinkage kinetics of silorane-based composites

      Composites used in this study

      Polymerization shrinkage (%) at 10 min, peak shrinkage rate (%/s), peak shrinkage time (s), and the inverse of peak shrinkage time (1/s) of composites

      Mean values with the same superscripts are not significantly different (p > 0.05).

      Number in parenthesis is standard deviation.

      Correlation analysis among polymerization shrinkage (%), peak shrinkage rate (%/s), peak shrinkage time (s), the inverse of peak time (1/s), and the product of polymerization shrinkage and the inverse of peak time of the composites

      Table 1 Composites used in this study

      Table 2 Polymerization shrinkage (%) at 10 min, peak shrinkage rate (%/s), peak shrinkage time (s), and the inverse of peak shrinkage time (1/s) of composites

      Mean values with the same superscripts are not significantly different (p > 0.05).

      Number in parenthesis is standard deviation.

      Table 3 Correlation analysis among polymerization shrinkage (%), peak shrinkage rate (%/s), peak shrinkage time (s), the inverse of peak time (1/s), and the product of polymerization shrinkage and the inverse of peak time of the composites


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