药物递送至眼部后节。
Drug delivery to the posterior segment of the eye.
机构信息
Drug Delivery Research Unit (DDRU), School of Pharmacy, Faculty of Medical and Health Sciences, The University of Auckland, Auckland 1010, New Zealand.
出版信息
Drug Discov Today. 2011 Mar;16(5-6):270-7. doi: 10.1016/j.drudis.2010.12.004. Epub 2010 Dec 15.
Delivery of drugs to the posterior eye is challenging, owing to anatomical and physiological constrains of the eye. There is an increasing need for managing rapidly progressing posterior eye diseases, such as age-related macular degeneration, diabetic retinopathy and retinitis pigmentosa. Drug delivery to the posterior segment of the eye is therefore compounded by the increasing number of new therapeutic entities (e.g. oligonucleotides, aptamers and antibodies) and the need for chronic therapy. Currently, the intravitreal route is widely used to deliver therapeutic entities to the retina. However, frequent administration of drugs via this route can lead to retinal detachment, endophthalmitis and increased intraocular pressure. Various controlled delivery systems, such as biodegradable and non-biodegradable implants, liposomes and nanoparticles, have been developed to overcome such adverse effects, with some success. The periocular route is a promising alternative, owing to the large surface area and the relatively high permeability of the sclera. Yet, the blood-retinal barrier and efflux transporters hamper the transport of therapeutic entities to the retina. As such, the efficient delivery of drugs to the posterior eye remains a major challenge facing the pharmaceutical scientist. In this review, we discuss the barriers of the posterior eye drug delivery and the various drug-delivery strategies used to overcome these barriers.
将药物递送至眼部后段具有挑战性,这归因于眼部的解剖学和生理学限制。人们越来越需要治疗诸如年龄相关性黄斑变性、糖尿病性视网膜病变和视网膜色素变性等快速进展性后眼部疾病。因此,由于越来越多的新型治疗实体(例如寡核苷酸、适体和抗体)以及需要慢性治疗,药物递送至眼部后段变得更加复杂。目前,玻璃体内途径被广泛用于将治疗实体递送至视网膜。然而,通过该途径频繁给药可能导致视网膜脱离、眼内炎和眼内压升高。已经开发了各种控释系统,例如可生物降解和不可生物降解的植入物、脂质体和纳米颗粒,以克服这些不良反应,并取得了一定的成功。由于巩膜的表面积大且相对较高的通透性,眼周途径是一种很有前途的替代途径。然而,血视网膜屏障和外排转运蛋白会阻碍治疗实体向视网膜的转运。因此,将药物高效递送至后眼部仍然是制药科学家面临的主要挑战。在这篇综述中,我们讨论了眼部后段药物递送的障碍以及用于克服这些障碍的各种药物递送策略。