Suppr超能文献

一种评估眼科溶液在细胞培养中随时间变化的定量细胞毒性的新方法。β-肾上腺素能阻滞剂。

A new method evaluating quantitative time-dependent cytotoxicity of ophthalmic solutions in cell culture. Beta-adrenergic blocking agents.

作者信息

Takahashi N

出版信息

Graefes Arch Clin Exp Ophthalmol. 1983;220(6):264-7. doi: 10.1007/BF00231353.

Abstract

A new method of evaluating quantitative cytotoxicity in cell culture was demonstrated using Chang's cultured human conjunctival cells. Time-dependent cytotoxicity of some beta-adrenergic blocking agents was shown and expressed by exposure time, causing 50% cell damage (50% cell damage time CDT50). Pure timolol maleate maleate of 0.25% and 0.5% concentration caused no cytotoxicity within a 64-min exposure. Pure befunolol hydrochloride of 0.25%, 0.5% and 1% inhibited 10%-30% of cell growth at 64-min exposure. Pure bupranolol of 0.125%, 0.25%, 0.5% and 1% showed evident cytotoxicity and CDT50 at 66 min 48 s, 38 min 54 s, 3 min 46 s and 1 min 18 s, respectively. Commercial preparations, which contained benzalkonium chloride as a preservative, indicated more rapid cytotoxicity. Timolol preparations of 0.25% and 0.5% showed CDT50 at 48.1 s and 2 min 4 s, respectively. Befunolol preparations of 0.25%, 0.5% and 1% showed CTD50 at 43.4% s, 4 min 38 s and 58 s, respectively, Bupranolol preparations of 0.125%, 0.25%, 0.5% and 1% demonstrated CDT50 at 1 min 11 s, 3 min 24 s, 22.3 s and 13.7 s, respectively.

摘要

利用张氏培养的人结膜细胞展示了一种评估细胞培养中定量细胞毒性的新方法。研究显示了一些β-肾上腺素能阻滞剂的时间依赖性细胞毒性,并通过暴露时间来表示,即导致50%细胞损伤的时间(50%细胞损伤时间CDT50)。0.25%和0.5%浓度的纯马来酸噻吗洛尔在64分钟的暴露时间内未产生细胞毒性。0.25%、0.5%和1%的纯盐酸倍他洛尔在64分钟暴露时抑制细胞生长10%-30%。0.125%、0.25%、0.5%和1%的纯布库洛尔分别在66分48秒、38分54秒、3分46秒和1分18秒表现出明显的细胞毒性和CDT50。含有苯扎氯铵作为防腐剂的商业制剂显示出更快的细胞毒性。0.25%和0.5%的噻吗洛尔制剂的CDT50分别为48.1秒和2分4秒。0.25%、0.5%和1%的倍他洛尔制剂的CTD50分别为43.4秒、4分38秒和58秒。0.125%、0.25%、0.5%和1%的布库洛尔制剂的CDT50分别为1分11秒、3分24秒、22.3秒和13.7秒。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验