Mishra Gyan P, Bagui Mahuya, Tamboli Viral, Mitra Ashim K
Division of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, 2464 Charlotte Street, Kansas City, MO 64108-2718, USA.
J Drug Deliv. 2011;2011:863734. doi: 10.1155/2011/863734. Epub 2011 Mar 1.
Liposomal formulations were significantly explored over the last decade for the ophthalmic drug delivery applications. These formulations are mainly composed of phosphatidylcholine (PC) and other constituents such as cholesterol and lipid-conjugated hydrophilic polymers. Liposomes are biodegradable and biocompatible in nature. Current approaches for topical delivery of liposomes are focused on improving the corneal adhesion and permeation by incorporating various bioadhesive and penetration enhancing polymers. In the case of posterior segment disorders improvement in intravitreal half life and targeted drug delivery to the retina is achieved by liposomes. In this paper we have attempted to summarize the applications of liposomes in the field of ophthalmic drug delivery by citing numerous investigators over the last decade.
在过去十年中,脂质体制剂在眼科药物递送应用方面得到了广泛研究。这些制剂主要由磷脂酰胆碱(PC)和其他成分如胆固醇以及脂质共轭亲水性聚合物组成。脂质体本质上具有生物可降解性和生物相容性。目前脂质体局部递送的方法主要集中在通过加入各种生物粘附和渗透增强聚合物来改善角膜粘附和渗透。对于后段疾病,脂质体可提高玻璃体内半衰期并实现药物向视网膜的靶向递送。在本文中,我们试图通过引用过去十年众多研究者的成果,总结脂质体在眼科药物递送领域的应用。