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一种高效且超长效的抗青光眼药物,具有新颖的眶周给药方法。

A Highly Effective and Ultra-Long-Acting Anti-Glaucoma Drug, with a Novel Periorbital Delivery Method.

机构信息

1 Department of Bioengineering, Imperial College London, South Kensington, London, England.

2 JeniVision, Inc., Irvine, California.

出版信息

J Ocul Pharmacol Ther. 2019 Jun;35(5):265-277. doi: 10.1089/jop.2018.0126. Epub 2019 Apr 25.

Abstract

Two features define the future of glaucoma therapeutics: (1) greatly improved ocular hypotensive efficacy and (2) a delivery method that improves patient convenience and compliance. A highly efficacious and extraordinarily long-acting ocular hypotensive agent PGN 9856-isopropyl ester represents a potential next-generation anti-glaucoma drug. A new periorbital drug delivery route was also investigated. PGN 9856-isopropyl ester pharmacology was determined by employing human cells, including prostanoid receptor transfectants, and FLIPr or cellular dielectric spectroscopy technology. Intraocular pressure (IOP) was measured in conscious cynomolgus monkeys trained to accept pneumatonometry when under gentle restraint. For periorbital application, the compound was applied radially using a roller-ball device connected to a cylindrical reservoir. Pharmacokinetic data were obtained using LC/MS/MS instrumentation. Single doses of PGN 9856-isopropyl ester, administered over a 0.001%-0.01% dose range, produced profound decreases in monkey IOP that persisted for at least 5 days, which was long after the drug was detectable in ocular tissues. It was not uncommon for a single eye drop to reduce IOP to the level of 4-7 mm Hg. Drug application to the periorbital dermis of ocular normotensive monkeys produced a similarly profound reduction in IOP, which was well maintained. PGN 9856-isopropyl ester appears to possess efficacy and duration of action properties unmatched by currently prescribed anti-glaucoma agents and by those currently undergoing clinical evaluation. In addition, application to the periorbital skin using a roller-ball device offers a more convenient method of ophthalmic drug delivery than eye drops and is noninvasive, unlike other "dropless" technologies.

摘要

两种特性定义了青光眼治疗的未来

(1)极大提高眼部降压效果,(2)改善患者便利性和顺应性的给药方法。一种高效且作用时间极长的眼部降压剂 PGN 9856-异丙酯代表了潜在的下一代抗青光眼药物。还研究了一种新的眶周药物递送途径。PGN 9856-异丙酯的药理学通过使用包括前列腺素受体转染体和 FLIPr 或细胞介电光谱技术的人细胞来确定。在接受轻柔约束的情况下接受气动眼压测量训练的清醒食蟹猴中测量眼内压 (IOP)。对于眶周应用,通过连接到圆柱形储液器的滚轮球装置将化合物以放射状方式施用。使用 LC/MS/MS 仪器获得药代动力学数据。PGN 9856-异丙酯的单剂量给药范围为 0.001%至 0.01%,可使猴子的 IOP 显著降低,至少持续 5 天,远超过眼部组织中可检测到药物的时间。单次滴眼即可将 IOP 降低到 4-7mmHg 水平并不罕见。将药物施用于眼正常的猴眶周真皮会产生类似程度的眼压降低,并且保持良好。PGN 9856-异丙酯似乎具有目前规定的抗青光眼药物和正在进行临床评估的药物所无法比拟的疗效和作用持续时间。此外,与滴眼相比,使用滚轮球装置将药物施用于眶周皮肤提供了一种更方便的眼部药物递送方法,并且不像其他“无滴”技术那样具有侵入性。

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