α-Lipoic Acid in Soluplus® Polymeric Nanomicelles for Ocular Treatment of Diabetes-Associated Corneal Diseases

被引:94
作者
Alvarez-Rivera, Fernando [1 ]
Fernandez-Villanueva, David [1 ]
Concheiro, Angel [1 ]
Alvarez-Lorenzo, Carmen [1 ]
机构
[1] Univ Santiago de Compostela, Fac Farm, Dept Farm & Tecnol Farmaceut, Grp GI 1645, Santiago De Compostela 15782, Spain
关键词
alpha-lipoic acid; micelle; solubility; diabetic keratopathy; HET-CAM assay; permeability; ophthalmic drug delivery; polymeric drug carrier; IN-VIVO PERMEATION; DRUG-DELIVERY; VITRO; MICELLES; SYSTEMS; MODEL; SOLUBILIZATION; COMPLICATIONS; PHOTOSHOP(R); FORMULATIONS;
D O I
10.1016/j.xphs.2016.03.006
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
alpha-Lipoic acid (ALA) is a powerful antioxidant valuable for prevention and treatment of ophthalmic complications such as diabetic keratopathy and retinopathy. The aim of this work was to develop micelle-based formulations that can enhance the solubility, stability, and corneal permeability of ALA. Compared to a conventional surfactant (sodium dioctylsulfosuccinate), Soluplus (R) (polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol copolymer) led to smaller micelles (70-80 vs. 240-528 nm) with improved ability to solubilize ALA, maintaining ocular compatibility (Hens Egg Test on the Chorio-Allantoic Membrane). Soluplus nanomicelles enhanced more than 10-fold ALA solubility compared to common eye drops and withstood strong dilution in lachrymal fluid, filtration through sterilizing membranes, and freeze-drying. Interestingly, Soluplus nanomicelle formulation prepared with 1 or 2 mM block copolymer concentration exhibited in situ gelling capability and transformed into weak gels at 35 degrees C, which is expected to increase corneal residence time. Bovine corneal permeability revealed that Soluplus nanomicelles notably enhanced ALA accumulation into the cornea as well as flux of drug toward the receptor chamber. Overall, these findings point out Soluplus nanomicelles as suitable carriers of ALA that may exhibit improved performance compared to currently available eye drop solutions. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:2855 / 2863
页数:9
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