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玻璃体内、结膜下和滴眼给予后小 13kDa 结构域抗体在兔眼内组织分布和药代动力学研究。

Ocular tissue distribution and pharmacokinetic study of a small 13kDa domain antibody after intravitreal, subconjuctival and eye drop administration in rabbits.

机构信息

GlaxoSmithKline, BioPharm Research and Development, Gunnels Wood Road, Stevenage, Hertfordshire, UK.

GlaxoSmithKline Research and Development, Drug Metabolism and Pharmacokinetics, 709 Swedeland Road, King of Prussia, PA 19406, USA.

出版信息

Exp Eye Res. 2018 Feb;167:14-17. doi: 10.1016/j.exer.2017.10.021. Epub 2017 Oct 23.

DOI:10.1016/j.exer.2017.10.021
PMID:29074387
Abstract

Domain antibodies (dAb's) comprise the smallest functional unit of human IgG and can be targeted to a range of different soluble cytokine and receptor targets in the eye. In particular their small size may offer advantage for ocular tissue penetration and distribution. To investigate this we used a 13kDa tool molecule to undertake a preliminary short term ocular tissue distribution and pharmacokinetic study in the rabbit eye. The dAb was administered by the intravitreal or subconjunctival route or, as topical eye drops for up to five days and dAb concentrations measured in vitreous, aqueous, conjunctiva, choroid-RPE, retina, iris, sclera, and ciliary body. The observed elimination half-live of the dAb (~3 days) in vitreous showed a similar elimination rate to that of a much larger (∼50kDa) Fab fragment whilst the half-life following subconjunctival administration was ∼24 h and, after eye drop dosing the dAb was detectable in aqueous and conjunctiva. These preliminary data show that the intravitreal half-life of dAb's are similar to much larger antibody fragments, offering the potential to deliver significantly more drug to target on a molar basis with a single intravitreal injection potentially enabling dosing frequencies of once a month or less. Subconjunctival injection may provide short duration therapeutic levels of dAb to the anterior and posterior chamber whilst topical eye drop delivery of dAbs may be useful in front-of-eye disease. These data indicate that small domain antibodies may have utility in ophthalmology. Further studies are warranted.

摘要

结构域抗体(dAb)构成了人 IgG 的最小功能单位,可以靶向作用于一系列不同的可溶性细胞因子和眼部受体靶标。特别是它们的小尺寸可能有利于眼部组织穿透和分布。为了研究这一点,我们使用了一种 13kDa 的工具分子,在兔眼进行了初步的短期眼组织分布和药代动力学研究。通过玻璃体内或结膜下途径给予 dAb,或作为局部眼滴剂,持续 5 天,并测量玻璃体内、房水、结膜、脉络膜-RPE、视网膜、虹膜、巩膜和睫状体中的 dAb 浓度。在玻璃体内观察到的 dAb 消除半衰期(3 天)与大得多的(50kDa)Fab 片段的消除率相似,而结膜下给药后的半衰期约为 24 小时,滴眼后可在房水和结膜中检测到 dAb。这些初步数据表明,玻璃体内 dAb 的半衰期与更大的抗体片段相似,有可能在单次玻璃体内注射的基础上以摩尔为单位输送更多的药物,从而有可能实现每月一次或更低的给药频率。结膜下注射可能为前房和后房提供 dAb 的短期治疗水平,而局部滴眼给予 dAb 可能对眼前节疾病有用。这些数据表明,小的结构域抗体可能在眼科中有应用价值。需要进一步研究。

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