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人工晶状体的生物相容性。

Biocompatibility of Intraocular Lenses.

作者信息

Özyol Pelin, Özyol Erhan, Karel Fatih

机构信息

Muğla Sıtkı Koçman University Training and Research Hospital, Department of Ophthalmology, Muğla, Turkey.

Dünyagöz Hospital, Ophthalmology Clinic, Ankara, Turkey.

出版信息

Turk J Ophthalmol. 2017 Aug;47(4):221-225. doi: 10.4274/tjo.10437. Epub 2017 Aug 15.

Abstract

The performance of an intraocular lens is determined by several factors such as the surgical technique, surgical complications, intraocular lens biomaterial and design, and host reaction to the lens. The factor indicating the biocompatibility of an intraocular lens is the behavior of inflammatory and lens epithelial cells. Hence, the biocompatibility of intraocular lens materials is assessed in terms of uveal biocompatibility, based on the inflammatory foreign-body reaction of the eye against the implant, and in terms of capsular biocompatibility, determined by the relationship of the intraocular lens with residual lens epithelial cells within the capsular bag. Insufficient biocompatibility of intraocular lens materials may result in different clinical entities such as anterior capsule opacification, posterior capsule opacification, and lens epithelial cell ongrowth. Intraocular lenses are increasingly implanted much earlier in life in cases such as refractive lens exchange or pediatric intraocular lens implantation after congenital cataract surgery, and these lenses are expected to exhibit maximum performance for many decades. The materials used in intraocular lens manufacture should, therefore, ensure long-term uveal and capsular biocompatibility. In this article, we review the currently available materials used in the manufacture of intraocular lenses, especially with regard to their uveal and capsular biocompatibility, and discuss efforts to improve the biocompatibility of intraocular lenses.

摘要

人工晶状体的性能由多种因素决定,如手术技术、手术并发症、人工晶状体生物材料与设计以及机体对晶状体的反应。表明人工晶状体生物相容性的因素是炎症细胞和晶状体上皮细胞的行为。因此,人工晶状体材料的生物相容性根据葡萄膜生物相容性(基于眼睛对植入物的炎症性异物反应)和囊膜生物相容性(由人工晶状体与囊袋内残留晶状体上皮细胞的关系决定)进行评估。人工晶状体材料生物相容性不足可能导致不同的临床情况,如前囊膜混浊、后囊膜混浊和晶状体上皮细胞内生。在屈光性晶状体置换或先天性白内障手术后的儿童人工晶状体植入等情况下,人工晶状体越来越多地在生命早期植入,并且这些晶状体预计要在几十年内展现出最佳性能。因此,用于制造人工晶状体的材料应确保长期的葡萄膜和囊膜生物相容性。在本文中,我们综述了目前用于制造人工晶状体的材料,特别是关于它们的葡萄膜和囊膜生物相容性,并讨论了提高人工晶状体生物相容性的努力。

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