Liu C-M, Huang F-M, Yang L-C, Chou L S-S, Chou M-Y, Chang Y-C
Department of Periodontics, Chung Shan Medical University Hospital, Taichung, Taiwan.
J Oral Rehabil. 2004 Apr;31(4):368-72. doi: 10.1046/j.1365-2842.2003.01237.x.
The objective of this study was to determine the cytocompatibility of three different extracts of gingival retraction cords and to compare the cytotoxic effect of these materials on human gingival fibroblasts. Gingival retraction cords impregnated with aluminium sulphate (Gingi-Aid), dl-adrenaline HCl (Gingi-Pak) and non-drug-impregnated cord (Gingi-Plain) were eluted with culture medium for 10 min and 24 h. Cytotoxicity was judged using a tetrazolium bromide reduction assay. Our data demonstrated that gingival retraction cords applied alone almost completely inhibited cell viability (P < 0.05). In addition, the results also showed that the eluates from aluminium sulphate-impregnated cord, dl-adrenaline HCl-impregnated cord and non-drug-impregnated cord were cytotoxic to primary human gingival fibroblast cultures (P < 0.05). The cell viability of incubation of gingival fibroblasts containing 10-min eluates of aluminium sulphate, dl-adrenaline HCl and non-drug-impregnated cord was 61, 21 and 70%, respectively. The cell viability of incubation of gingival fibroblasts containing 24 h eluates of aluminium sulphate, dl-adrenaline HCl and non-drug-impregnated cord was 68, 58 and 72%, respectively. It was found that dl-adrenaline HCl-impregnated gingival retraction cord was the most toxic gingival retraction cord among the materials tested in all cultures (P < 0.05). The cytotoxicity decreased in an order of dl-adrenaline HCl-impregnated cord > aluminium sulphate-impregnated cord > non-drug-impregnated cord. The extent or degree of the cytotoxicity depended on the materials tested. Gingival retraction cords have significant potential for gingival toxicity. Careful management of gingiva retraction cords would lower the risk of potential gingival tissue damage during clinical application procedure and thus increase the success of prosthodontic procedures.
本研究的目的是确定三种不同牙龈收缩线提取物的细胞相容性,并比较这些材料对人牙龈成纤维细胞的细胞毒性作用。用含有硫酸铝(Gingi - Aid)、盐酸dl - 肾上腺素(Gingi - Pak)的牙龈收缩线以及无药物浸渍的线(Gingi - Plain)在培养基中洗脱10分钟和24小时。使用溴化四氮唑还原试验判断细胞毒性。我们的数据表明,单独使用牙龈收缩线几乎完全抑制细胞活力(P < 0.05)。此外,结果还显示,硫酸铝浸渍线、盐酸dl - 肾上腺素浸渍线和无药物浸渍线的洗脱液对原代人牙龈成纤维细胞培养物具有细胞毒性(P < 0.05)。含有硫酸铝、盐酸dl - 肾上腺素和无药物浸渍线10分钟洗脱液的牙龈成纤维细胞培养物的细胞活力分别为61%、21%和70%。含有硫酸铝、盐酸dl - 肾上腺素和无药物浸渍线24小时洗脱液的牙龈成纤维细胞培养物的细胞活力分别为68%、58%和72%。发现在所有培养物中测试的材料中,盐酸dl - 肾上腺素浸渍的牙龈收缩线是毒性最大的牙龈收缩线(P < 0.05)。细胞毒性按盐酸dl - 肾上腺素浸渍线>硫酸铝浸渍线>无药物浸渍线的顺序降低。细胞毒性的程度或大小取决于所测试的材料。牙龈收缩线具有显著的牙龈毒性潜力。在临床应用过程中,仔细处理牙龈收缩线将降低潜在牙龈组织损伤的风险,从而提高口腔修复手术的成功率。