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[用于临床的VLC Dycal在组织培养中的细胞毒性评估]

[Evaluation of cytotoxicity of VLC Dycal in tissue culture for clinical use].

作者信息

Kaga M, Seale N S, Oikawa K

出版信息

Shoni Shikagaku Zasshi. 1989;27(2):313-6.

PMID:2535151
Abstract

The purpose of this study was to evaluate the VLC Dycal (visible light cured composite-calcium hydroxide material) to see whether it is suitable or not as a direct or indirect pulp capping agent for clinical use by means of the cell culture test. Two light cured composite resins, P-30 and Silux, and also Dycal and Ca(OH)2 were used as a control for a comparative cytotoxicity test with VLC Dycal. All test materials were put into the glass tubes (4 mm diameter X 1 mm high), then illuminated for 10, 20, 30, 40, 50 and 60 seconds through a matrix strip with direct contact with a Prisma-light source (L.D. Caulk), just before testing. Fibroblasts, 5 ml of 1 X 10(5) cells per ml in Eagle's MEM medium with 10% FCS, penicillin (100 U/ml) and streptomycin (100 micrograms/ml) were evenly seeded on a cover glass in a tissue culture dish and incubated for 24 hours at 37 degrees C in a humidified atmosphere of a 5% CO2 in air. After 24 hours, the medium was replaced with 5 ml of agar overlay medium consisting of 10% FCS, Eagle's MEM medium and 1.5% agar. Glass tubes (n = 8) filled with the test materials were placed at the center of the agar, and incubated for 24 hours in 5% CO2 in air at 37 degrees C. After 24 hours of incubation, the cover glass was removed and the cells were fixed in 10% neutral formalin and then stained by H.E. to differentiate the areas of affected and unaffected cells beneath the test specimens. The affected area was quantitatively determined using an image analysis system.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是通过细胞培养试验评估可见光固化Dycal(可见光固化复合氢氧化钙材料)作为直接或间接牙髓盖髓剂用于临床是否合适。使用两种光固化复合树脂P-30和Silux,以及Dycal和Ca(OH)2作为对照,与VLC Dycal进行比较细胞毒性试验。所有测试材料放入玻璃管(直径4毫米×高1毫米)中,在测试前通过与Prisma光源(L.D. Caulk)直接接触的基质条照射10、20、30、40、50和60秒。将5毫升每毫升含1×10(5)个细胞的成纤维细胞接种于含有10%胎牛血清、青霉素(100 U/ml)和链霉素(100微克/ml)的伊格尔氏MEM培养基中,均匀接种于组织培养皿中的盖玻片上,在37℃、5%二氧化碳的潮湿空气中孵育24小时。24小时后,用5毫升由10%胎牛血清、伊格尔氏MEM培养基和1.5%琼脂组成的琼脂覆盖培养基替换培养基。将装有测试材料的玻璃管(n = 8)置于琼脂中央,在37℃、5%二氧化碳的空气中孵育24小时。孵育24小时后,取出盖玻片,将细胞固定于10%中性福尔马林中,然后用苏木精-伊红染色以区分测试标本下方受影响和未受影响的细胞区域。使用图像分析系统对受影响区域进行定量测定。(摘要截短于250字)

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