Uptake and Release of Dexamethasone Phosphate From Silicone Hydrogel and Group I, II, and IV Hydrogel Contact Lenses

被引:71
|
作者
Boone, Adrienne [1 ]
Hui, Alex [1 ]
Jones, Lyndon [1 ]
机构
[1] Univ Waterloo, Ctr Contact Lens Res, Sch Optometry, Waterloo, ON N2L 3G1, Canada
来源
基金
加拿大自然科学与工程研究理事会;
关键词
Dexamethasone; Silicone hydrogel; Contact lens; Drug delivery; Bandage lens; OPHTHALMIC DRUG-DELIVERY; EXTENDED-WEAR; BENZALKONIUM CHLORIDE; HYDROPHILIC LENS; BANDAGE LENSES; ACUTE GLAUCOMA; HEMA HYDROGEL; SOFT; MANAGEMENT; PRESERVATIVES;
D O I
10.1097/ICL.0b013e3181b26c49
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objectives: To investigate the uptake and release kinetics of the synthetic glucocorticoid anti-inflammatory drug dexamethasone into various conventional and silicone hydrogel contact lens materials. Methods: Three conventional and six silicone hydrogel lenses were used in this study. A 0.1% dexamethasone solution was formulated and used to dope the various contact lens materials. The uptake and release of the drug was measured using a UV-visible light spectrophotometer at various time points during a period of 24 hr for each phase. Results: Statistical analysis showed that all lenses took up a significant amount of dexamethasone. Alphafilcon A and lotrafilcon A showed the greatest uptake of dexamethasone, at 118 +/- 10 mu g/lens and 102 +/- 11 mu g/lens, respectively, and galyfilcon took up the least amount of drug at 34 +/- 6 mu g/lens. The release of the drug from the lens materials was also statistically significant. The majority of the lenses released between 20 and 30 mu g/lens, except for alphafilcon A and lotrafilcon A, which released a statistically different amount of drug when compared with the other lens materials. Alphafilcon A released 65 +/- 1.3 mu g/lens, whereas lotrafilcon A slowly released only 11 +/- 0.2 mu g/lens. Conclusions: Although most of the lenses released enough drug to have anti-inflammatory action, none of the materials released drug for a long enough period of time to be clinically useful as a drug delivery device.
引用
收藏
页码:260 / 267
页数:8
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