首页> 外文期刊>Biocontrol Science >Comparative Study of In Vitro Ocular Surface Cytotoxicity of a Fixed Combination of 0.5% Timolol/1% Dorzolamide Eyedrop and Its Components with 0.005% Benzalkonium Chloride
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Comparative Study of In Vitro Ocular Surface Cytotoxicity of a Fixed Combination of 0.5% Timolol/1% Dorzolamide Eyedrop and Its Components with 0.005% Benzalkonium Chloride

机译:0.5%Timolol / 1%Dorzolamide滴眼液及其成分与0.005%苯扎氯铵固定组合的体外眼表面细胞毒性比较研究

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We evaluated the cytotoxicity of antiglaucoma ophthalmic solutions preserved with the same concentration of benzalkonium chloride (BAK) in four cultured corneal and conjunctival cell lines. The viability of cell cultures was determined following the exposure of cells to timolol maleate, dorzolamide, and their fixed combination, Kosoputo (MSD, a Japanese formulation of Cosopt (Merck) ) , and two commercially available eyedrop solutions, 0.5% Timpotol (containing 0.5% timolol maleate, MSD) and 1% Trusopt (containing 1% dorzolamide, MSD) for varying exposure times and at various dilutions using the MTT and neutral red assays. All the three commercially available eyedrop solutions tested in this study were preserved with 0.005% BAK. The toxicity of each solution was compared using the % cell viability score (CVS) . Cell viability was also subjected to statistical analysis using ANOVA, Dunnett's multiple comparison tests and a chi-square test. %CVS50/%CVS40/80s for the tested solutions were 53/-13 for 0.5% Timoptol, 100/88 for preservative-free 0.5% timolol maleate, 50/ -10 for 1% Trusopt, 72/100 for preservative-free 1% dorzolamide, and 44/ -17 for Kosoputo. The results of statistical analysis were consistent to them. In conclusion, Kosoputo had greater cytotoxicity than each component; however, in actual use it may have the advantages of reduced toxicity (side effect) due to reduced instillation frequency, and better patient adherence to the treatment regimen as well as a comparable pressure reduction effect.
机译:我们评估了在四个培养的角膜和结膜细胞系中用相同浓度的苯扎氯铵(BAK)保存的抗青光眼眼药水的细胞毒性。在将细胞暴露于马来酸替莫洛尔,多佐胺及其固定组合Kosoputo(MSD,日本Cosopt(Merck)制剂)和两种市售滴眼液0.5%Timpotol(含0.5%)后,确定细胞培养物的活力。使用MTT和中性红检测方法,可以改变曝光时间并以各种稀释度使用不同浓度的%马来酸替莫洛尔(MSD)和1%Trusopt(含1%多唑胺,MSD)。本研究中测试的所有三种市售滴眼液均用0.005%BAK保存。使用%细胞生存力分数(CVS)比较每种溶液的毒性。还使用ANOVA,Dunnett的多重比较测试和卡方检验对细胞活力进行了统计分析。被测溶液的%CVS50 /%CVS40 / 80s对于0.5%Timoptol为53 / -13,对于不含防腐剂的0.5%马来酸替莫洛尔为100/88,对于1%Trusopt为50 / -10,对于不含防腐剂为72/100 %的多佐胺,Kosoputo的浓度为44 / -17。统计分析的结果与他们一致。总之,Kosoputo具有比每种成分更大的细胞毒性。但是,在实际使用中,由于降低了滴注频率,具有降低毒性(副作用)的优点,并且患者对治疗方案的依从性更好,并且具有类似的减压效果。

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