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义齿基托树脂的细胞毒性:水浴和微波后聚合热处理的影响

Cytotoxicity of denture base resins: effect of water bath and microwave postpolymerization heat treatments.

作者信息

Jorge Janaina Habib, Giampaolo Eunice Teresinha, Vergani Carlos Eduardo, Machado Ana Lúcia, Pavarina Ana Cláudia, Carlos Iracilda Zeppone

机构信息

Department of Dental Materials and Prosthodontics, São Paulo State University, Araraquara Dental School, São Paulo, Brazil.

出版信息

Int J Prosthodont. 2004 May-Jun;17(3):340-4.

Abstract

PURPOSE

This study compared the effect of two postpolymerization heat treatments on the cytotoxicity of three denture base resins on L929 cells using 3H-thymidine incorporation and MTT assays.

MATERIALS AND METHODS

Sample disks of Lucitone 550, QC 20, and Acron MC resins were fabricated under aseptic conditions and stored in distilled water at 37 degrees C for 48 hours. Specimens were then divided into three groups: (1) heat treated in microwave oven for 3 minutes at 500 W; (2) heat treated in water bath at 55 degrees C for 60 minutes; and (3) no heat treatment. Eluates were prepared by placing three disks into a sterile glass vial with 9 mL of Eagle's medium and incubating at 37 degrees C for 24 hours. The cytotoxic effect from the eluates was evaluated using the 3H-thymidine incorporation and MTT assays, which reflect DNA synthesis levels and cell metabolism, respectively.

RESULTS

The components leached from the resins were cytotoxic to L929 cells when 3H-thymidine incorporation assay was employed. In contrast, eluates from all resins revealed noncytotoxic effects as measured by MTT assay. For both MTT assay and 3H-thymidine incorporation, the heat treatments did not decrease the cytotoxicity of the materials tested.

CONCLUSION

Resins were graded by 3H-thymidine incorporation assay as slightly cytotoxic and by MTT assay as noncytotoxic. Cytotoxicity of the denture base materials was not influenced by microwave or water bath heat treatment.

摘要

目的

本研究使用3H-胸腺嘧啶核苷掺入法和MTT法,比较两种聚合后热处理对三种义齿基托树脂对L929细胞的细胞毒性的影响。

材料与方法

在无菌条件下制作Lucitone 550、QC 20和Acron MC树脂的样本盘,并于37℃蒸馏水中储存48小时。然后将样本分为三组:(1)在微波炉中以500W功率加热3分钟;(2)在55℃水浴中加热60分钟;(3)不进行热处理。通过将三个样本盘放入含有9mL伊格尔培养基的无菌玻璃瓶中,于37℃孵育24小时来制备洗脱液。使用3H-胸腺嘧啶核苷掺入法和MTT法评估洗脱液的细胞毒性作用,这两种方法分别反映DNA合成水平和细胞代谢情况。

结果

当采用3H-胸腺嘧啶核苷掺入法时,树脂中浸出的成分对L929细胞具有细胞毒性。相比之下,通过MTT法测定,所有树脂的洗脱液均显示无细胞毒性作用。对于MTT法和3H-胸腺嘧啶核苷掺入法,热处理均未降低所测试材料的细胞毒性。

结论

通过3H-胸腺嘧啶核苷掺入法评定树脂具有轻微细胞毒性,而通过MTT法评定为无细胞毒性。义齿基托材料的细胞毒性不受微波或水浴热处理的影响。

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