Erdal Nejla B, Adolfsson Karin H, De Lima Sara, Hakkarainen Minna
Department of Fibre and Polymer Technology, KTH Royal Institute of Technology, Stockholm, Sweden.
Department of Clinical Neuroscience, Division of Ophthalmology and Vision, St. Erik Eye Hospital, Karolinska Institutet, Stockholm, Sweden.
Clin Exp Optom. 2018 May;101(3):354-362. doi: 10.1111/cxo.12652. Epub 2018 Jan 11.
Acuvue Oasys silicone hydrogel contact lenses (Senofilcon A) are used as bandage lenses and often combined with ophthalmic solutions in the treatment of ocular diseases. Concerns have been raised regarding the compatibility and effect of eye-drop solutions on the bandage lenses, which have led to frequent replacement of lenses causing clinical problems. Some patients experience pain or discomfort during treatments and the accumulation of drugs and preservatives in lenses has been suggested as a possible reason. The aim with this study was to investigate the effect of ophthalmic solutions on silicone hydrogel bandage lens material Senofilcon A in vitro and in vivo.
The effect of three common ophthalmic solutions Isopto-Maxidex, Timosan and Oftaquix on Acuvue Oasys (Senofilcon A) bandage lenses was evaluated. An in vitro model method was developed where drug and preservative uptake by Acuvue Oasys was monitored with ultraviolet-visible spectroscopy and laser desorption ionisation mass spectrometry. Surface morphology changes of the lenses were evaluated using scanning electron microscopy. The method was then implemented for the in vivo pilot study evaluating lenses worn by patients.
In vitro model study monitoring the drug and preservatives uptake showed that the active ingredients from all the eye drops together with preservatives were taken up by the lenses in significant amounts. For the in vivo study no traces of active ingredients or preservatives could be found on the worn and treated lenses regardless of time being worn or dosage profiles. The surface morphology changes in the in vivo study were also minor in contrast to the changes observed in the in vitro scanning electron microscopy images.
The in vivo results demonstrate minor effects of the ophthalmic solutions on the worn lenses. These results do not support the building up of preservatives and drugs on the contact lenses as the cause of pain or discomfort experienced by some patients, which is encouraging for the use of bandage lenses in combination with ophthalmic solutions.
酷柏欧舒适氧硅水凝胶隐形眼镜(senofilcon A)用作绷带镜,常用于眼部疾病治疗并常与眼药水联合使用。眼药水与绷带镜的兼容性及效果引发关注,这导致频繁更换镜片,引发临床问题。部分患者在治疗期间会感到疼痛或不适,镜片中药物和防腐剂的积聚被认为是可能原因。本研究旨在体外和体内研究眼药水对硅水凝胶绷带镜材料senofilcon A的影响。
评估了三种常用眼药水(妥布霉素地塞米松、替马西泮和左氧氟沙星)对酷柏欧舒适氧(senofilcon A)绷带镜的影响。开发了一种体外模型方法,用紫外可见光谱和激光解吸电离质谱监测酷柏欧舒适氧对药物和防腐剂的摄取。用扫描电子显微镜评估镜片的表面形态变化。然后将该方法用于评估患者佩戴镜片的体内初步研究。
监测药物和防腐剂摄取的体外模型研究表明,所有眼药水的活性成分以及防腐剂都大量被镜片吸收。在体内研究中,无论佩戴时间或用药情况如何,在佩戴和处理过的镜片上均未发现活性成分或防腐剂的痕迹。与体外扫描电子显微镜图像中观察到的变化相比,体内研究中的表面形态变化也较小。
体内研究结果表明眼药水对佩戴的镜片影响较小。这些结果不支持将隐形眼镜上防腐剂和药物的积聚作为一些患者疼痛或不适的原因,这对于绷带镜与眼药水联合使用是一个鼓舞。