首页> 外文期刊>Investigative ophthalmology & visual science >Efficient intraocular penetration of topical anti-TNF-alpha single-chain antibody (ESBA105) to anterior and posterior segment without penetration enhancer.
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Efficient intraocular penetration of topical anti-TNF-alpha single-chain antibody (ESBA105) to anterior and posterior segment without penetration enhancer.

机译:局部抗TNF-α单链抗体(ESBA105)高效眼内渗透至前段和后段,而无渗透增强剂。

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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 onfrequency 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.
机译:目的:本研究旨在表征眼前段和后段ESBA105(一种针对肿瘤坏死因子(TNF)-α的局部给药单链抗体(scFv))的眼部渗透途径。方法:将新鲜去角质全眼和安装在灌注室中的家兔角膜用于离体穿透研究。研究了玻璃体内注射或滴眼液局部给药后ESBA105的体内药代动力学和眼生物分布。结果:在不使用渗透促进剂的情况下,以眼药水局部给药后,ESBA105在眼的前部和后部达到治疗水平。 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7小时的血清半衰期相比,ESBA105在玻璃体内的消除半衰期显着延长,为25小时。行政。因此,基于局部给药的频率,可以实现ESBA105积累到玻璃体内不同的稳态水平。结论:ESBA105局部给药可快速达到前段和后段的治疗水平,而无需任何渗透促进剂。用作眼药水的ESBA105的药物渗透性和眼部生物分布模式在临床上用于治疗眼睛的TNF-α依赖性疾病显得非常有吸引力。

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