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牙本质调节剂和底漆对人牙周膜细胞的体外细胞毒性

Cytotoxicity of dentin conditioners and primers on human periodontal ligament cells in vitro.

作者信息

Kinomoto Yoshifumi, Carnes David L, Ebisu Shigeyuki

机构信息

Department of Restorative Dentistry and Endodontology, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Am J Dent. 2003 Apr;16(2):125-8.

PMID:12797572
Abstract

PURPOSE

To examine the cytotoxicity of dentin conditioners and primers on human periodontal ligament (PDL) cells in vitro.

MATERIALS AND METHODS

Primary PDL cells were plated in 96 well culture plates and exposed to 100 microL of test solutions. Undiluted Cavity Conditioner (CC), Vitremer Primer (VP), Uni-Etch (UE), All-Bond 2 (AB), Gluma conditioner (GC), and Gluma primer (GP) were examined at full strength and at 1/100 and 1/1000 dilutions in culture medium. Cytotoxicity of the undiluted material was determined immediately following exposure of the cells to the test substance. Cytotoxicity of the diluted materials was determined immediately following a 300-second exposure of the cells to the test solution, as well as 24 hours after removal of the test solution. Cytotoxicity was expressed as lactate dehydrogenase activity retained within the cells following exposure divided by the activity in unexposed control cells.

RESULTS

Exposure to each undiluted test substance resulted in severe damage to the cells (78.2-100%). At 1/100 dilution, only exposure to UE resulted in significant cytotoxicity (72.9%) immediately following removal of the solution. But significant cytotoxicity (21-100%) was evident in cells 24 hours after removal of each of the materials. At 1/1000 dilution, exposure to UE (14.8%) and GP (27.2%) resulted in mild cytotoxicity. Twenty-four hours after removal of the solutions, there was a mild but significant cytotoxic effect of each of the test substances (18.5-49.4%).

摘要

目的

体外检测牙本质调节剂和底漆对人牙周膜(PDL)细胞的细胞毒性。

材料与方法

将原代PDL细胞接种于96孔培养板中,暴露于100微升测试溶液中。对未稀释的窝洞调节剂(CC)、Vitremer底漆(VP)、Uni-Etch(UE)、全粘结剂2(AB)、Gluma调节剂(GC)和Gluma底漆(GP)在培养基中进行原液、1/100和1/1000稀释后进行检测。细胞暴露于测试物质后立即测定未稀释材料的细胞毒性。稀释材料的细胞毒性在细胞暴露于测试溶液300秒后以及去除测试溶液24小时后立即测定。细胞毒性以暴露后细胞内保留的乳酸脱氢酶活性除以未暴露对照细胞中的活性来表示。

结果

暴露于每种未稀释的测试物质均导致细胞严重损伤(78.2 - 100%)。在1/100稀释时,仅暴露于UE在去除溶液后立即导致显著的细胞毒性(72.9%)。但在去除每种材料24小时后,细胞中明显出现显著的细胞毒性(21 - 100%)。在1/1000稀释时,暴露于UE(14.8%)和GP(27.2%)导致轻度细胞毒性。去除溶液24小时后,每种测试物质均有轻度但显著的细胞毒性作用(18.5 - 49.4%)。

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