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每日一次 0.6%贝那利珠单抗滴眼液的眼部生物分布显示,给药后 24 小时内最高浓度在结膜。

Ocular Biodistribution of Once-Daily 0.6% Bilastine Eye Drops Reveals Highest Levels in Conjunctiva Up to 24 h Postadministration.

机构信息

Research, Development and Innovation Department (R&D+i Department), Faes Farma, Bizkaia, Spain.

出版信息

J Ocul Pharmacol Ther. 2022 Nov;38(9):617-625. doi: 10.1089/jop.2022.0024. Epub 2022 Oct 21.

DOI:10.1089/jop.2022.0024
PMID:36269652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9700334/
Abstract

Bilastine is a second-generation antihistamine that has been shown to be effective for treatment of allergic conjunctivitis. The objective of this study was to evaluate the pharmacokinetics (PKs) and biodistribution of 0.6% bilastine preservative-free eye drops. Bilastine was quantified in the conjunctiva, cornea, aqueous humor, vitreous humor, iris/ciliary body, retina/choroid, crystalline lens, and plasma, following a single topical administration to male Dutch-belted rabbits. Concentrations of bilastine were highest in the conjunctiva [C: 2,545.04 ng/g, at 6 h postadministration; area under the concentration-time curve (AUC): 11,382.40 ng·h/g] and cornea (C: 609.11 ng/g, at 1 h postadministration; AUC: 1,993.88 ng·h/g), followed by the iris/ciliary body, retina/choroid, aqueous humor, plasma, vitreous humor, and crystalline lens. Quantifiable bilastine concentrations were observed up to 24 h after instillation in the conjunctiva (388.45 ng/g), cornea (28.68 ng/g), iris/ciliary body (12.42 ng/g), retina/choroid (1.91 ng/g), and crystalline lens (0.12 ng/g). In plasma, aqueous humor, and vitreous humor, bilastine was detected up to 12 h postadministration (0.18 ng/mL, 0.40 ng/mL, and 0.32 ng/g, respectively). PKs and biodistribution of 0.6% bilastine eye drops in rabbits revealed a marked preferential distribution in the conjunctiva (target tissue), with sustained levels up to 24 h. These findings are consistent with clinical efficacy trials supporting once-daily administration of topical bilastine for treatment of allergic conjunctivitis.

摘要

比拉斯汀是一种第二代抗组胺药,已被证明可有效治疗过敏性结膜炎。本研究旨在评估 0.6%比拉斯汀无防腐剂滴眼液的药代动力学(PKs)和生物分布。在单次局部给药后,比拉斯汀在雄性荷兰垂耳兔的结膜、角膜、房水、玻璃体、虹膜/睫状体、视网膜/脉络膜、晶状体和血浆中进行定量。在给药后 6 小时,结膜中的比拉斯汀浓度最高 [C:2545.04ng/g,AUC:11382.40ng·h/g],角膜次之 [C:609.11ng/g,AUC:1993.88ng·h/g],随后是虹膜/睫状体、视网膜/脉络膜、房水、血浆、玻璃体和晶状体。在结膜(388.45ng/g)、角膜(28.68ng/g)、虹膜/睫状体(12.42ng/g)、视网膜/脉络膜(1.91ng/g)和晶状体(0.12ng/g)中,在滴眼后 24 小时内均可检测到可量化的比拉斯汀浓度。在血浆、房水和玻璃体中,在滴眼后 12 小时内可检测到比拉斯汀(分别为 0.18ng/mL、0.40ng/mL 和 0.32ng/g)。0.6%比拉斯汀滴眼液在兔中的 PKs 和生物分布显示,其在结膜(靶组织)中具有明显的优先分布,可持续达 24 小时。这些发现与支持每日一次局部应用比拉斯汀治疗过敏性结膜炎的临床疗效试验一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab1/9700334/41b8a5d0256a/jop.2022.0024_figure2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab1/9700334/c92b4be9a9ea/jop.2022.0024_figure1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab1/9700334/41b8a5d0256a/jop.2022.0024_figure2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab1/9700334/c92b4be9a9ea/jop.2022.0024_figure1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab1/9700334/41b8a5d0256a/jop.2022.0024_figure2.jpg

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