生物相容性
药物输送
维甲酸
药品
药理学
体内
化学
视网膜
微球
生物医学工程
医学
生物化学
有机化学
生物技术
工程类
基因
生物
化学工程
作者
Fengxiang Wang,Shou-zhi He,Bin Chen
标识
DOI:10.1016/j.biopha.2017.10.109
摘要
Pharmacotherapy were the mainstream methods for the treatment of proliferative vitreoretinopathy (PVR), one of the leading causes of blindness. Due to the negligible side-effects, retinoic acid (RA) was considered to be a promising candidate drug. However, it was still a challenge to deliver drugs into vitreous with both long-term efficiency and biosafety. Sodium alginate was considered to be an excellent drug carrier owing to its controlled size, good biocompatibility and degradability. Based on a one-time synthetic strategy of preparing RA-sodium alginate microspheres, the study was aimed to establish a non-toxic and effective RA slow release platform. The prepared microspheres were smoothly round and relatively homogenous with an average diameter of 95.7±9.6μm. RA release rate from RA-MS was assessed in vitro by UV spectrometry and in vivo by high performance liquid chromatography, achieving a steady, long-term and effective level of RA. The biocompatibility of RA-MS was further confirmed through histology using HE staining and fundus microscope, finding no inflammation and other toxic response. Collectively, it could be concluded that RA-MS possessed a great potential in retinal PVR treatment.
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