Maliba Pharmacy College, Uka Tarsadia University, Surat 394350, India.
Biomater Sci. 2018 May 29;6(6):1580-1591. doi: 10.1039/c8bm00212f.
Glaucoma is a chronic disease, which is currently treated using frequent high dose applications of an eye drop solution; this method is tedious, and most of patients are non-compliant to it. Contact lenses are emerging as a convenient option to sustain the release of ophthalmic drugs. However, the incorporation of a drug/formulation changes the optical and physical properties of contact lenses. Contact lens users have also reported pink eye syndrome; this makes contact lenses unsuitable to be accepted as a medical device. The objective of the present study was to design novel timolol and hyaluronic acid (comfort agent)-loaded semi-circular ring-implanted contact lenses that could uphold the release at therapeutic rates without compromising the critical lens properties. The drug-loaded rings were individually implanted within the periphery of the contact lenses using modified cast-moulding technology. Atomic force microscopy showed an average roughness of 12.38 nm for the implanted lens that was significantly lower as compared to that of the Freshlook contact lenses (116.27 nm). A major amount of timolol was leached (from 46.47 to 58.79%) during the monomer extraction and moist sterilization (autoclave) steps; therefore, the lenses were sterilized by radiation and packaged under dry conditions (dehydrated). The in vitro release data showed sustained release of timolol and hyaluronic acid up to 96 h. The in vivo drug release study on rabbit eyes showed the presence of timolol in tear fluid up to 72 h. The in vivo pharmacodynamics studies showed a reduction in IOP till 144 h with a low drug loading (154 μg) as compared to the case of a single instillation eye drop solution (250 μg). This study has demonstrated the successful application of implantation technology to co-deliver timolol and hyaluronic acid from contact lenses for an extended period of time to treat glaucoma.
青光眼是一种慢性疾病,目前的治疗方法是频繁使用高剂量的眼药水滴注;这种方法繁琐,大多数患者都不遵守。隐形眼镜作为一种方便的选择,正在出现以维持眼科药物的释放。然而,药物/配方的加入改变了隐形眼镜的光学和物理性质。隐形眼镜使用者也报告了眼睛发红综合征;这使得隐形眼镜不适合被接受为医疗器械。本研究的目的是设计新型噻吗洛尔和透明质酸(舒适剂)负载的半圆形环植入隐形眼镜,可以在不影响关键镜片特性的情况下以治疗速率维持释放。使用改良的铸模技术,将载药环单独植入隐形眼镜的周边。原子力显微镜显示,植入镜片的平均粗糙度为 12.38nm,明显低于 Freshlook 隐形眼镜(116.27nm)。噻吗洛尔的大部分在单体提取和湿消毒(高压灭菌)步骤中被浸出(从 46.47%到 58.79%);因此,镜片通过辐射消毒,并在干燥条件下(脱水)包装。体外释放数据显示噻吗洛尔和透明质酸持续释放长达 96 小时。兔眼体内药物释放研究表明,噻吗洛尔在泪液中存在长达 72 小时。体内药效学研究表明,与单次滴眼溶液(250μg)相比,在低药物载量(154μg)的情况下,眼压降低至 144 小时。这项研究证明了植入技术成功地应用于从隐形眼镜中共同输送噻吗洛尔和透明质酸,以延长时间治疗青光眼。