Tacrolimus 0.1% Ophthalmic Suspension: Corneal and Intraocular Penetration Study.

IF 1.9 4区 医学 Q2 OPHTHALMOLOGY
Maxime Quirke, Fabien Lamoureux, Christophe Arnoult, Gladys Gress, Ariella Ganem, Théophile Charpentier, Marc Muraine, Julie Gueudry
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Abstract

Purpose: Topical tacrolimus is currently used in ocular surface pathologies as a corticosteroid-sparing immunosuppressive agent. It could also help prevent endothelial corneal graft rejection and inflammatory diseases; however, its hydrophobic nature and high molecular weight theoretically limit its intraocular penetration. The aim of this study is to investigate the corneal and intraocular penetration of a 0.1% tacrolimus ophthalmic suspension. Methods: Sixteen rabbits were randomly spread into four groups defined by the delay between the last tacrolimus instillation and corneal sampling (2, 6, 11, and 24 h). Three rabbits per group received bilateral instillations of tacrolimus twice daily for 5 days, the 4th subject in each group serving as negative controls. The 5th day, conjunctiva, corneal epithelium, anterior stroma, posterior stroma, corneal endothelium, iris, choroid/retina, aqueous humor, and plasma samples were collected. Tacrolimus concentrations were determined using high-performance liquid chromatography coupled with tandem mass spectrometry. Results: Maximum mean concentration was reached after 2 h in the epithelium, anterior and posterior stroma, and endothelium: 12794 (±2656), 436 (±178), 341 (±179), and 4125 (±1673) ng/g, respectively. The descending rank order of exposure over 24 h was: corneal epithelium; corneal endothelium; conjunctiva; anterior stroma; posterior stroma; iris; and chorioretina with 158.0; 39.99; 4.620; 4.134; 3.350; 0.384; 0.270 ng.h/mg, respectively. Conclusions: Tacrolimus concentrations measured in the corneal tissues are significantly higher than that described as lower limit of efficacy in solid organ transplantation. Topical 0.1% tacrolimus could therefore become an alternative to corticosteroids for endothelial graft rejection prevention and endothelial inflammatory pathologies management.

0.1%他克莫司眼用混悬液:角膜和眼内渗透研究。
目的:局部他克莫司目前作为一种保留皮质类固醇的免疫抑制剂用于眼表病变。它还可以帮助预防角膜内皮移植排斥反应和炎症性疾病;然而,它的疏水性和高分子量理论上限制了其眼内渗透。本研究的目的是研究0.1%他克莫司眼用混悬液的角膜和眼内渗透。方法:16只家兔按最后一次他克莫司滴注至角膜取样的延迟时间(2、6、11、24 h)随机分为4组。每组3只兔双侧滴注他克莫司,每日2次,连续5 d,每组4只兔为阴性对照。第5天,采集结膜、角膜上皮、前基质、后基质、角膜内皮、虹膜、脉络膜/视网膜、房水和血浆样本。采用高效液相色谱-串联质谱法测定他克莫司浓度。结果:2 h后,上皮、前、后间质和内皮细胞的最大平均浓度分别为12794(±2656)、436(±178)、341(±179)和4125(±1673)ng/g。24 h内暴露程度由高到低依次为:角膜上皮;角膜内皮;结膜;前基质;后基质;虹膜;绒毛膜蛋白为158.0;39.99;4.620;4.134;3.350;0.384;0.270 ng.h/mg。结论:他克莫司在角膜组织中的浓度明显高于实体器官移植的有效下限。因此,局部0.1%他克莫司可能成为皮质类固醇的替代品,用于预防内皮移植排斥反应和内皮炎症病理管理。
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来源期刊
CiteScore
4.60
自引率
4.30%
发文量
72
审稿时长
1 months
期刊介绍: Journal of Ocular Pharmacology and Therapeutics is the only peer-reviewed journal that combines the fields of ophthalmology and pharmacology to enable optimal treatment and prevention of ocular diseases and disorders. The Journal delivers the latest discoveries in the pharmacokinetics and pharmacodynamics of therapeutics for the treatment of ophthalmic disorders. Journal of Ocular Pharmacology and Therapeutics coverage includes: Glaucoma Cataracts Retinal degeneration Ocular infection, trauma, and toxicology Ocular drug delivery and biotransformation Ocular pharmacotherapy/clinical trials Ocular inflammatory and immune disorders Gene and cell-based therapies Ocular metabolic disorders Ocular ischemia and blood flow Proliferative disorders of the eye Eyes on Drug Discovery - written by Gary D. Novack, PhD, featuring the latest updates on drug and device pipeline developments as well as policy/regulatory changes by the FDA.
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