Optimized release of dexamethasone and gentamicin from a soluble ocular insert for the treatment of external ophthalmic infections

被引:29
作者
Baeyens, V
Kaltsatos, V
Boisrame, B
Varesio, E
Veuthey, JL
Fathi, M
Balant, LP
Gex-Fabry, M
Gurny, R
机构
[1] Univ Geneva, Sch Pharm, CH-1211 Geneva 4, Switzerland
[2] Magny Vernois, Vetoquinol, F-70204 Lure, France
[3] Univ Geneva, Lab Pharmaceut Analyt Chem, CH-1211 Geneva 4, Switzerland
[4] Hop Cantonal Univ Geneva, Toxicol Lab, CH-1211 Geneva 14, Switzerland
[5] Psychiat Univ Inst Geneva, Clin Res Unit, CH-1225 Chene Bourg, Switzerland
关键词
dexamethasone; gentamicin; insert; in vivo release; ocular drug delivery;
D O I
10.1016/S0168-3659(97)00212-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the case of external ophthalmic infections, repeated instillations of antibiotics are required to reach therapeutic level, above the minimal inhibitory concentration (MIG). An additional administration of a corticosteroid is often needed, in order to limit the precorneal damages caused by the infection. However, repeated administration of a corticosteroid can increase intraocular pressure and thus lead to glaucoma. To overcome the disadvantages of separated and repeated instillations of two products and to avoid the side effects of dexamethasone, a soluble insert containing gentamicin sulfate and dexamethasone phosphate was developed. The new system ensures the concomitant release of the two drugs during the first 10 h of treatment, followed by an adequate concentration of gentamicin sulfate, above the MIC of 4.0 mu g ml(-1), during 50 h, due to a combination of gentamicin sulfate with cellulose acetate phthalate, which reduces the solubility of gentamicin. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:215 / 220
页数:6
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