Tanti Nicole C, Jones Lyndon, Gorbet Maud B
Department of Systems Design Engineering, University of Waterloo, Waterloo, Ontario, Canada.
Optom Vis Sci. 2011 Apr;88(4):483-92. doi: 10.1097/OPX.0b013e3182045967.
To assess, in vitro, the effect of the release of contact lens multipurpose solutions (MPS) from two silicone hydrogel lenses on human corneal epithelial cells.
A monolayer of immortalized human corneal epithelial cells was seeded in a 24-well plate in keratinocyte serum-free medium. Lotrafilcon A (LA) and balafilcon A (BA) lenses were placed on top of the adherent cells for 8 and 24 h, after being soaked in MPS, borate-buffered (Unisol) or phosphate-buffered saline overnight. Cells were assayed for viability using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay or for α3, β1, and β4 integrin expression and caspase activation by flow cytometry.
After 8 h, LA lenses soaked in Unisol, Opti-Free Express (OFX), and ReNu MultiPlus (ReNu) showed decrease in cell viability. LA and BA soaked in Complete Moisture Plus (Complete) had similar viability at around 85% of control. After 24 h, a further decrease in viability was observed with all MPS-soaked lenses; LA soaked in OFX significantly reduced viability compared with Unisol-soaked lenses. In addition, reduced levels of integrin expression for lenses soaked in OFX and ReNu, and for BA soaked in Complete were observed. At 24 h, only LA soaked in OFX led to an increase in caspase activation.
Our results indicate an increase in cytotoxicity with borate-based MPS solutions in vitro when compared with both phosphate-buffered saline and borate-exposed lenses, suggesting that biocides and/or additives play a role in the observed cell reaction. Moreover, the mechanism of in vitro solution-induced toxicity appeared to be mediated by lens type, suggesting differences in the preferential adsorption/release profile of certain compounds.
在体外评估两种硅水凝胶镜片释放的隐形眼镜多功能护理液(MPS)对人角膜上皮细胞的影响。
将永生化人角膜上皮细胞单层接种于24孔板中的角质形成细胞无血清培养基中。洛替拉康A(LA)和百视明A(BA)镜片在浸泡于MPS、硼酸盐缓冲液(Unisol)或磷酸盐缓冲盐水中过夜后,放置在贴壁细胞上8小时和24小时。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法检测细胞活力,或通过流式细胞术检测α3、β1和β4整合素表达以及半胱天冬酶激活情况。
8小时后,浸泡于Unisol、Opti-Free Express(OFX)和ReNu MultiPlus(ReNu)中的LA镜片显示细胞活力下降。浸泡于Complete Moisture Plus(Complete)中的LA和BA活力相似,约为对照组的85%。24小时后,所有浸泡于MPS的镜片活力进一步下降;浸泡于OFX中的LA与浸泡于Unisol中的镜片相比,活力显著降低。此外,观察到浸泡于OFX和ReNu中的镜片以及浸泡于Complete中的BA的整合素表达水平降低。在24小时时,仅浸泡于OFX中的LA导致半胱天冬酶激活增加。
我们的结果表明,与磷酸盐缓冲盐水和暴露于硼酸盐的镜片相比,基于硼酸盐的MPS溶液在体外的细胞毒性增加,这表明杀菌剂和/或添加剂在观察到的细胞反应中起作用。此外,体外溶液诱导毒性的机制似乎由镜片类型介导,表明某些化合物的优先吸附/释放特征存在差异。