Poly-(cyclo)dextrins as ethoxzolamide carriers in ophthalmic solutions and in contact lenses

被引:46
作者
Garcia-Fernandez, M. J. [1 ]
Tabary, N. [2 ]
Martel, B. [2 ]
Cazaux, F. [2 ]
Oliva, A. [3 ]
Taboada, P. [4 ]
Concheiro, A. [1 ]
Alvarez-Lorenzo, C. [1 ]
机构
[1] Univ Santiago de Compostela, Fac Farm, Dept Farm & Tecnol Farmaceut, Santiago De Compostela 15782, Spain
[2] Univ Lille 1, Unite Mat & Transformat UMET, F-59655 Villeneuve Dascq, France
[3] Univ La Laguna, Fac Farm, Dept Ingn Quim & Tecnol Farmaceut, Tenerife 38200, Spain
[4] Univ Santiago de Compostela, Fac Fis, Dept Fis Mat Condensada, Santiago De Compostela 15782, Spain
关键词
Cyclodextrin polymer; Ethoxzolamide solubilization; Glaucoma; Acrylic hydrogel; Inclusion complex; Sustained release; DRUG-DELIVERY; CYCLODEXTRIN POLYMER; SUSTAINED-RELEASE; CITRIC-ACID; IN-VITRO; GELS; HYDROGELS; SOLUBILIZATION; FABRICS;
D O I
10.1016/j.carbpol.2013.08.003
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Efficient ophthalmic therapy requires the development of strategies that can provide sufficiently high drug levels in the ocular structures for a prolonged time. This work focuses on the suitability of poly(cyclo)dextrins as carriers able to solubilize the carbonic anhydrase inhibitor (CAI) ethoxzolamide (ETOX), which is so far used for oral treatment of glaucoma. Topical ocular treatment should notably enhance the efficiency/safety profile of the drug. Natural alpha-, beta- and gamma-cyclodextrins and a maltodextrin were separately polymerized using citric acid as cross-linker agent under mild conditions. The resultant hydrophilic polymers exhibited larger capability to solubilize ETOX than the pristine (cyclo)dextrins. Moreover, they provided sustained drug diffusion in artificial lachrymal fluid. Interestingly the poly-(cyclo)dextrins solutions facilitate the loading of remarkably high doses of ETOX in poly(2-hydroxyethyl methacrylate)-based contact lenses. Exploiting ionic interactions between functional groups in the contact lenses and remnant free carboxylic acids in the citric acid linkers of poly-(cyclo)dextrins led to the retention of the drug-loaded poly-(cyclo)dextrins and, in turn, to sustained release for several weeks. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1343 / 1352
页数:10
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