Laboratory of Biohybrid Technologies, Institute of Chemistry, St. Petersburg State University, Peterhoff Campus, Universitetskii pr. 26, 198504, St. Petersburg, Russia.
Drug Research Program, Faculty of Pharmacy, University of Helsinki, Viikinkaari 5 E, 00790, Helsinki, Finland.
Small. 2019 Apr;15(15):e1805199. doi: 10.1002/smll.201805199. Epub 2019 Mar 14.
The previously published report suggests that liposomes, functionalized with annexin-5, can deliver bevacizumab to the retina after topical administration as eyedrops. Topical delivery of bevacizumab would be an attractive alternative to the current treatment that involves monthly intravitreal injections to the eye. In this Comment, the retinal concentrations of topically applied liposomal bevacizumab are compared to the levels reached after intravitreal injections. The comparison reveals that the topical liposomal delivery results in retinal bevacizumab concentrations that are about 3-5 orders of magnitude below the lowest bevacizumab concentrations during clinical treatment with intravitreal injections. Major improvement is needed before topical bevacizumab delivery can be considered clinically feasible.
先前发表的报告表明,经 annexin-5 功能化的脂质体,通过局部滴眼的方式就可以将贝伐单抗递送至视网膜。与目前每月向眼内注射的治疗方法相比,局部递送贝伐单抗将是一种有吸引力的替代方法。在本评论中,比较了局部应用的脂质体贝伐单抗在视网膜中的浓度与玻璃体内注射后达到的水平。比较结果表明,局部脂质体递送导致视网膜中的贝伐单抗浓度约比玻璃体内注射临床治疗时的最低贝伐单抗浓度低 3-5 个数量级。在考虑将局部贝伐单抗给药用于临床之前,需要进行重大改进。