Ocular Delivery of Flurbiprofen Based on Eudragit® E-Flurbiprofen Complex Dispersed in Aqueous Solution: Preparation, Characterization, In Vitro Corneal Penetration, and Ocular Irritation

被引:25
作者
Alejandra Quinteros, Daniela [1 ]
Ignacio Tartara, Luis
Daniel Palma, Santiago
Hilario Manzo, Ruben
Alberto Allemandi, Daniel
机构
[1] Univ Nacl Cordoba, CONICET, Unidad Invest & Desarrollo Tecnol Farmaceut UNITE, RA-5000 Cordoba, Argentina
关键词
flurbiprofen; Eudragit; complex; ophthalmic solution; Permeability; Polymeric drug delivery systems; Controlled release; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ANIONIC DRUGS; RELEASE; E100; PERMEABILITY; EQUILIBRIUM; PARTICLES; TOLERANCE; POLYMERS; NSAIDS;
D O I
10.1002/jps.24153
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A novel ophthalmic formulation based on the ionic complexation between Eudragit E 100 (EU) and flurbiprofen (FB) is proposed. The selected complex composition, named EU-FBH50Cl50, had the basic groups of EU completely neutralized with equal molar amounts of FB and HCl. This complex, obtained in the solid state, exhibited a high aqueous compatibility producing a colloidal dispersion with a high positive electrokinetic potential, in which more than 99% of FB was ionically condensed with EU. In bicompartimental Franz cells, FB diffusion from the complex was very slow. However, dispersion in 0.9% NaCl increased the FB release through an ionic exchange, providing an optimal constant rate of delivery. Corneal FB permeation from 0.1% EU-FBH50-Cl-50 dispersed in 0.9% NaCl solution was substantially more effective compared with 0.1% FB solution, EU-FBH50-Cl-50(Dex), or Tolerane((R)) (a marketed formulation). This complex formulation was shown to be innocuous for rabbit ocular tissues because no irritant effects were evidenced. (c) 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 103:3859-3868, 2014
引用
收藏
页码:3859 / 3868
页数:10
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