Sigurdsson Hakon H, Konráethsdóttir Fífa, Loftsson Thorsteinn, Stefánsson Einar
Faculty of Pharmacy, University of Iceland, Reykjavik, Iceland.
Acta Ophthalmol Scand. 2007 Sep;85(6):598-602. doi: 10.1111/j.1600-0420.2007.00885.x. Epub 2007 Jul 23.
This study aimed to: (1) determine the relative efficiencies of topical and systemic absorption of drugs delivered by eyedrops to the anterior and posterior segments of the eye; (2) establish whether dexamethasone-cyclodextrin eyedrops deliver significant levels of drug to the retina and vitreous in the rabbit eye, and (3) compare systemic absorption following topical application to the eye versus intranasal or intravenous delivery.
In order to distinguish between topical and systemic absorption in the eye, we applied 0.5% dexamethasone-cyclodextrin eyedrops to one (study) eye of rabbits and not to the contralateral (control) eye. Drug levels were measured in each eye. The study eye showed the result of the combination of topical and systemic absorption, whereas the control eye showed the result of systemic absorption only. Systemic absorption was also examined after intranasal and intravenous administration of the same dose of dexamethasone.
In the aqueous humour dexamethasone levels were 170 +/- 76 ng/g (mean +/- standard deviation) in the study eye and 6 +/- 2 ng/g in the control eye. Similar ratios were seen in the iris and ciliary body. In the retina the dexamethasone level was 33 +/- 7 ng/g in the study eye and 14 +/- 3 ng/g in the control eye. Similar ratios were seen in the vitreous humour. Systemic absorption was similar from ocular, intranasal and intravenous administration.
Absorption after topical application dominates in the anterior segment. Topical absorption also plays a significant role in delivering dexamethasone to the posterior segment of the rabbit eye. In medication administered to the retina, 40% of the drug reaches the retina via the systemic route and 60% via topical penetration. Dexamethasone-cyclodextrin eyedrops deliver a significant amount of drug to the rabbit retina.
本研究旨在:(1)确定滴眼液给药后药物在前段和后段眼组织中的局部和全身吸收的相对效率;(2)确定地塞米松 - 环糊精滴眼液是否能将显著水平的药物递送至兔眼的视网膜和玻璃体,以及(3)比较眼部局部应用与鼻内或静脉给药后的全身吸收情况。
为区分眼部的局部和全身吸收,我们给兔的一只(研究)眼滴入0.5%地塞米松 - 环糊精滴眼液,对侧(对照)眼不滴药。测量每只眼中的药物水平。研究眼显示局部和全身吸收的综合结果,而对照眼仅显示全身吸收的结果。在鼻内和静脉注射相同剂量的地塞米松后也检测全身吸收情况。
在房水中,研究眼的地塞米松水平为170±76 ng/g(平均值±标准差),对照眼为6±2 ng/g。虹膜和睫状体中也观察到类似的比例。在视网膜中,研究眼的地塞米松水平为33±7 ng/g,对照眼为14±3 ng/g。玻璃体中也观察到类似的比例。眼部、鼻内和静脉给药后的全身吸收情况相似。
局部应用后的吸收在前段占主导。局部吸收在将地塞米松递送至兔眼后段中也起重要作用。在视网膜给药中,40%的药物通过全身途径到达视网膜,60%通过局部渗透到达。地塞米松 - 环糊精滴眼液可将大量药物递送至兔视网膜。