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局部抗TNF-α单链抗体(ESBA105)在无渗透促进剂的情况下对眼内前后节的高效穿透。

Efficient intraocular penetration of topical anti-TNF-alpha single-chain antibody (ESBA105) to anterior and posterior segment without penetration enhancer.

作者信息

Ottiger Michael, Thiel Michael A, Feige Ulrich, Lichtlen Peter, Urech David M

机构信息

ESBATech AG, Schlieren, Switzerland.

出版信息

Invest Ophthalmol Vis Sci. 2009 Feb;50(2):779-86. doi: 10.1167/iovs.08-2372. Epub 2008 Aug 29.

Abstract

PURPOSE

This study was designed to characterize ocular penetration pathways of ESBA105, a topically administered single-chain antibody (scFv) against tumor necrosis factor (TNF)-alpha, to the anterior and posterior segment of the eye.

METHODS

Fresh enucleated whole eyes and isolated corneas of rabbits mounted in perfusion chambers were used for ex vivo penetration studies. In vivo pharmacokinetics and ocular biodistribution of ESBA105 after intravitreal injection or topical administration as eye drops were investigated in rabbits.

RESULTS

After topical administration as eye drops, without a penetration enhancer, ESBA105 reached therapeutic levels in the anterior and posterior segment of the eye. ESBA105 migrated to aqueous humor via corneal penetration and vitreous and retina via intrascleral penetration pathways. In vivo, ESBA105 had a significantly prolonged elimination half-life in the vitreous of 25 hours compared with its serum half-life of 7 hours after i.v. administration. Therefore, based on frequency of topical dosing, a buildup of ESBA105 to distinct steady state levels in the vitreous could be achieved.

CONCLUSIONS

Topically administered ESBA105 quickly reaches therapeutic levels in the anterior and posterior segment without any need for a penetration enhancer. Drug penetration and ocular biodistribution patterns of ESBA105 applied as eye drops appear highly attractive for clinical use to treat TNF-alpha dependant diseases of the eye.

摘要

目的

本研究旨在表征ESBA105(一种局部给药的抗肿瘤坏死因子(TNF)-α单链抗体(scFv))在眼的前段和后段的眼内渗透途径。

方法

将新鲜摘除的兔全眼和安装在灌注室中的分离角膜用于体外渗透研究。在兔体内研究了玻璃体内注射或滴眼局部给药后ESBA105的体内药代动力学和眼内生物分布。

结果

滴眼局部给药后,在没有渗透促进剂的情况下,ESBA105在眼的前段和后段达到治疗水平。ESBA105通过角膜渗透迁移至房水,并通过巩膜内渗透途径迁移至玻璃体和视网膜。在体内,与静脉注射后血清半衰期7小时相比,ESBA105在玻璃体内的消除半衰期显著延长至25小时。因此,基于局部给药频率,可以使ESBA105在玻璃体内积累至不同的稳态水平。

结论

局部给药的ESBA105无需任何渗透促进剂即可迅速在眼的前段和后段达到治疗水平。作为滴眼液应用的ESBA105的药物渗透和眼内生物分布模式对于治疗眼的TNF-α依赖性疾病的临床应用似乎极具吸引力。

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