Institute of Ocular Pharmacology, School of Ophthalmology and Optometry, Wenzhou Medical College, 270 Xueyuan Road, Wenzhou, Zhejiang 325027, China.
Br J Ophthalmol. 2010 May;94(5):654-8. doi: 10.1136/bjo.2009.172106.
AIM To characterise the pharmacokinetics of triamcinolone acetonide (TA) in various ocular tissues following a single sub-Tenon injection. METHODS Twenty-one Chinchilla adult pigmented rabbits received sub-Tenon injection of TA (40 mg in 0.4 ml) in their right eyes. Three animals were killed at each designated time points (3 h, 1 day, 3 days, 7 days, 14 days, 21 days and 30 days) and the globes were snap frozen and dissected into aqueous, iris-ciliary body, vitreous, neuroretina and retinal pigment epithelium (RPE)/choroid. The concentrations of TA in the various ocular tissues were analysed using ultra-performance liquid chromatography, coupled with tandem mass spectrometric detection. RESULTS TA concentration followed a mono-exponential decrease over the study period in all ocular tissues of the injected eyes. The concentration was much higher in the RPE/choroid (892.14+/-558.11 ng/g at post-injection day 30) than in the other tissues (171.65+/-136.40 ng/g in neuroretina, 15.65+/-23.06 ng/ml in vitreous, 3.76+/-1.79 ng/g in iris-ciliary body, 2.64+/-0.96 ng/ml in aqueous at post-injection day 30). The TA level in the RPE/choroid had the lowest coefficient of logarithmic regression (0.07 in RPE/choroid, 0.10 in neuroretina, 0.11 in vitreous, 0.17 in iris-ciliary body, 0.18 in aqueous), indicating a 2.6 times slower clearance than in aqueous. The half-life of TA was 10.4 days in RPE/choroid. TA was detectable in the fellow eyes and was also detectable at very low levels in all blood samples during the entire study period. CONCLUSION TA was mostly cleared from RPE/choroid and retina in a mono-exponential mode. TA was above the therapeutic level for at least 30 days following a sub-Tenon injection.
描述单次玻璃体内注射曲安奈德(TA)后在各种眼部组织中的药代动力学特征。
21 只成年青紫蓝兔右眼接受玻璃体内注射 TA(0.4ml 中 40mg)。每个指定时间点(3h、1d、3d、7d、14d、21d 和 30d)处死 3 只动物,眼球立即冷冻并解剖为房水、虹膜睫状体、玻璃体、神经视网膜和视网膜色素上皮(RPE)/脉络膜。采用超高效液相色谱-串联质谱法检测分析 TA 在各种眼部组织中的浓度。
TA 浓度在研究期间呈单指数下降,在注射眼的所有眼部组织中均如此。在 RPE/脉络膜中的浓度(注射后 30 天的 892.14+/-558.11ng/g)远高于其他组织(神经视网膜中的 171.65+/-136.40ng/g,玻璃体中的 15.65+/-23.06ng/ml,虹膜睫状体中的 3.76+/-1.79ng/g,房水中的 2.64+/-0.96ng/ml)。RPE/脉络膜中的 TA 水平对数回归系数最低(RPE/脉络膜中为 0.07,神经视网膜中为 0.10,玻璃体中为 0.11,虹膜睫状体中为 0.17,房水中为 0.18),表明清除速度比房水慢 2.6 倍。RPE/脉络膜中 TA 的半衰期为 10.4 天。在整个研究期间,TA 可在对侧眼和所有血液样本中检测到,且均处于低水平。
TA 主要以单指数模式从 RPE/脉络膜和视网膜中清除。玻璃体内注射 TA 后至少 30 天,TA 浓度仍处于治疗水平之上。