Parr Gregory R, Rueggeberg Frederick A
Department of Oral Rehabilitation, School of Dentistry, The Medical College of Georgia, Augusta, GA 30912-1260, USA.
J Prosthet Dent. 2002 Aug;88(2):139-44. doi: 10.1067/mpr.2002.127399.
The clinical properties of resilient denture liners may be influenced by the method by which they are polymerized.
This in vitro study investigated material property changes of 2 new resilient denture lining materials that represent 2 different curing modes: autopolymerization and conventional laboratory processing.
Two silicone-based liner products were tested; one was allowed to autopolymerize (Tokuyama Soft Relining Paste), and the other was laboratory processed (Luci-Sof). Ninety-six disk-shaped specimens (31 x 10 mm) were fabricated in aluminum ring molds for hardness testing. Sixty bar-shaped specimens (44 x 8.5 x 1.2 mm) were fabricated in aluminum molds for water sorption and resin solubility testing. Shore A hardness was determined directly after specimen fabrication and after 1 day, 1 week, 1 month, 6 months, and 1 year of water storage at 37 degrees C. Water sorption and resin solubility were determined at the same time intervals. Analysis of variance and appropriate t tests were used to determine the effect of immersion duration both within and between the products tested. All statistical testing was performed at alpha=.05.
The hardness values of the laboratory-processed material were consistently greater than those of the autopolymerized material. After 1 week of water storage, the hardness of the autopolymerized specimens stabilized, whereas the hardness of the laboratory-processed specimens increased with immersion duration. Water sorption values for the 2 test products were similar after 6 months and after 1 year of water storage. At 1 month, 6 months, and 1 year, significantly lower resin solubility (P<.05) was recorded for the autopolymerized specimens compared with their laboratory-processed counterparts.
Within the limitations of this study, the laboratory-processed material was harder than the autopolymerized product and demonstrated greater resin solubility over time. The latter result was not expected.
弹性义齿衬垫的临床特性可能会受到其聚合方法的影响。
本体外研究调查了两种代表不同固化模式的新型弹性义齿衬垫材料的材料性能变化:自凝聚合和传统实验室加工。
测试了两种硅酮基衬垫产品;一种进行自凝聚合(德山软衬糊剂),另一种进行实验室加工(露西软衬)。在铝环模具中制作96个圆盘形试样(31×10毫米)用于硬度测试。在铝模具中制作60个条形试样(44×8.5×1.2毫米)用于吸水性和树脂溶解性测试。在试样制作后以及在37℃下储存1天、1周、1个月、6个月和1年的水后,直接测定邵氏A硬度。在相同时间间隔测定吸水性和树脂溶解性。使用方差分析和适当的t检验来确定浸泡时间对所测试产品内部和之间的影响。所有统计测试均在α=0.05水平进行。
实验室加工材料的硬度值始终高于自凝聚合材料。储存1周后,自凝聚合试样的硬度稳定,而实验室加工试样的硬度随浸泡时间增加。两种测试产品在储存6个月和1年后的吸水性值相似。在1个月、6个月和1年时,与实验室加工的试样相比,自凝聚合试样的树脂溶解性显著降低(P<0.05)。
在本研究的局限性内,实验室加工的材料比自凝聚合产品更硬,并且随着时间的推移显示出更大的树脂溶解性。后一个结果出乎意料。