Graham B S, Jones D W, Sutow E J
Department of Restorative Dentistry, Faculty of Dentistry, Dalhousie University, Halifax, Nova Scotia, Canada.
J Dent Res. 1991 May;70(5):870-3. doi: 10.1177/00220345910700050101.
Polymer-gel materials used as short-term denture soft linings are blended with plasticizers to lower the glass transition temperature (Tg). A lower Tg allows for greater polymer chain mobility, thus producing a more flexible material. The present work evaluated the loss of plasticizers due to leaching both in vivo and in vitro. Two commercial denture soft-lining materials (A and B) were tested. These were both poly(ethyl methacrylate) polymers, blended with alcohol and phthalate esters. A clinical study was conducted in which patients wore, sequentially, dentures bearing (on separate occasions) each of the two soft-polymer lining materials. The two materials A and B were randomly assigned for each of ten patients and were worn for 14 and 30 days, respectively. With one exception, patients wore dentures with both lining materials, for a total of 19 clinical evaluations. The plasticizer loss occurring during the clinical trial was determined by GC analysis from the initial and terminal day sampling of plasticizer content of the soft polymer-gel materials. The results of this analysis were compared with results obtained from an in vitro leachability study by use of sink conditions in water at 37 degrees C for the same two commercial soft polymers conducted over the same time periods of 14 and 30 days. The results indicated that a higher loss of plasticizer occurred in vivo, compared with the in vitro tests for 17 of the 19 clinical evaluations. The average plasticizer lost in vivo from material A at 14 days was 122 +/- 58 mg/g, and for material B at 30 days it was 33 +/- 27 mg/g.(ABSTRACT TRUNCATED AT 250 WORDS)
用作短期义齿软衬里的聚合物凝胶材料与增塑剂混合以降低玻璃化转变温度(Tg)。较低的Tg允许更大的聚合物链流动性,从而产生更柔韧的材料。本研究评估了体内和体外增塑剂因浸出而导致的损失。测试了两种商用义齿软衬里材料(A和B)。它们均为聚(甲基丙烯酸乙酯)聚合物,与醇和邻苯二甲酸酯混合。进行了一项临床研究,患者依次佩戴分别带有两种软聚合物衬里材料之一的义齿(在不同场合)。两种材料A和B被随机分配给十名患者中的每一位,分别佩戴14天和30天。除一个例外,患者佩戴了带有两种衬里材料的义齿,共进行了19次临床评估。通过气相色谱分析,从软聚合物凝胶材料增塑剂含量的初始和末期采样确定临床试验期间发生的增塑剂损失。将该分析结果与在37摄氏度水中使用水槽条件对相同两种商用软聚合物在14天和30天相同时间段内进行的体外浸出性研究结果进行比较。结果表明,在19次临床评估中的17次中,与体外测试相比,体内增塑剂损失更高。材料A在14天时体内平均损失的增塑剂为122±58mg/g,材料B在30天时为33±27mg/g。(摘要截短于250字)