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功能化聚硅氧烷作为可注射、原位固化的适应性眼内透镜。

Functionalised polysiloxanes as injectable, in situ curable accommodating intraocular lenses.

机构信息

CSIRO Molecular and Health Technologies, Bayview Avenue, Clayton, VIC 3168, Australia.

出版信息

Biomaterials. 2010 Nov;31(32):8153-63. doi: 10.1016/j.biomaterials.2010.07.065. Epub 2010 Aug 7.

Abstract

The aged eye's ability to change focus (accommodation) may be restored by replacing the hardened natural lens with a soft gel. Functionalised polysiloxane macromonomers, designed for application as an injectable, in situ curable accommodating intraocular lens (A-IOL), were prepared via a two-step synthesis. Prepolymers were synthesised via ring opening polymerisation (ROP) of octamethylcyclotetrasiloxane (D(4)) and 2,4,6,8-tetramethylcyclotetrasiloxane (D(4)(H)) in toluene using trifluoromethanesulfonic acid (TfOH) as catalyst. Hexaethyldisiloxane (HEDS) was used as the end group to control the molecular weight of the prepolymers, which were then converted to macromonomers by hydrosilylation of the SiH groups with allyl methacrylate (AM) to introduce polymerisable groups. The resulting macromonomers had an injectable consistency and thus, were able to be injected into and refill the empty lens capsular bag. The macromonomers also contained a low ratio of polymerisable groups so that they may be cured on demand, in situ, under irradiation of blue light, in the presence of a photo-initiator, to form a soft polysiloxane gel (an intraocular lens) in the eye. The pre-cure viscosity and post-cure modulus of the polysiloxanes, which are crucial factors for an injectable, in situ curable A-IOL application, were controlled by adjusting the end group and D(4)(H) concentrations, respectively, in the ROP. The macromonomers were fully cured within 5 min under light irradiation, as shown by the rapid change in modulus monitored by photo-rheology. Ex vivo primate lens stretching experiments on an Ex Vivo Accommodation Simulator (EVAS) showed that the polysiloxane gel refilled lenses achieved over 60% of the accommodation amplitude of the natural lens. An in vivo biocompatibility study in rabbits using the lens refilling (Phaco-Ersatz) procedure demonstrated that the soft gels had good biocompatibility with the ocular tissue. The polysiloxane macromonomers meet the targeted optical and mechanical properties of a young natural crystalline lens and show promise as candidate materials for use as injectable, in situ curable A-IOLs for lens refilling procedures.

摘要

老化眼睛的焦点(调节)变化能力可以通过用软凝胶代替硬化的天然晶状体来恢复。功能性聚硅氧烷大分子单体,设计用作可注射的原位固化调节型眼内透镜(A-IOL),通过两步合成制备。预聚物通过八甲基环四硅氧烷(D(4))和 2,4,6,8-四甲基环四硅氧烷(D(4)(H))在甲苯中的开环聚合(ROP)在三氟甲磺酸(TfOH)作为催化剂合成。六乙基二硅氧烷(HEDS)用作端基以控制预聚物的分子量,然后通过硅氢加成将 SiH 基团与甲基丙烯酰氧基丙基三甲氧基硅烷(AM)转化为大分子单体,以引入可聚合基团。所得大分子单体具有可注射的稠度,因此能够注入并填充空的晶状体囊袋。大分子单体还含有低比例的可聚合基团,因此它们可以在需要时原位固化,在存在光引发剂的情况下,在蓝光照射下,形成软的聚硅氧烷凝胶(眼内透镜)。聚硅氧烷的预固化粘度和后固化模量是可注射的、原位固化的 A-IOL 应用的关键因素,通过调整 ROP 中的端基和 D(4)(H)浓度来控制。大分子单体在光照射下 5 分钟内完全固化,如通过光流变学监测的模量快速变化所示。在 Ex Vivo Accommodation Simulator (EVAS) 上进行的离体灵长类晶状体拉伸实验表明,聚硅氧烷凝胶填充的晶状体实现了天然晶状体调节幅度的 60%以上。在兔体内进行的使用晶状体填充(Phaco-Ersatz)程序的生物相容性研究表明,软凝胶与眼部组织具有良好的生物相容性。聚硅氧烷大分子单体满足年轻天然晶状体的目标光学和机械性能,并有望成为用作晶状体填充程序的可注射的原位固化 A-IOL 的候选材料。

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