In Situ Gelling Electrospun Ocular Films Sustain the Intraocular Pressure-Lowering Effect of Timolol Maleate: In Vitro, Ex Vivo, and Pharmacodynamic Assessment

噻吗洛尔 眼压 体内 离体 青光眼 药理学 化学 药物输送 生物医学工程 材料科学 眼科 体外 医学 纳米技术 生物化学 生物技术 生物
作者
Ioannis I. Andreadis,Christina Karavasili,Angelos Thomas,Anastasia Komnenou,Manolis Tzimtzimis,Dimitrios Tzetzis,Dimitrios Andreadis,Nikolaos Bouropoulos,Dimitrios G. Fatouros
出处
期刊:Molecular Pharmaceutics [American Chemical Society]
卷期号:19 (1): 274-286 被引量:20
标识
DOI:10.1021/acs.molpharmaceut.1c00766
摘要

Most common intraocular pressure (IOP) reduction regimens for the management of glaucoma include the topical use of eye drops, a dosage form that is associated with short residence time at the site of action, increased dosing frequency, and reduced patient compliance. In situ gelling nanofiber films comprising poly(vinyl alcohol) and Poloxamer 407 were fabricated via electrospinning for the ocular delivery of timolol maleate (TM), aiming to sustain the IOP-lowering effect of the β-blocker, compared to conventional eye drops. The electrospinning process was optimized, and the physicochemical properties of the developed formulations were thoroughly investigated. The fiber diameters of the drug-loaded films ranged between 123 and 145 nm and the drug content between 5.85 and 7.83% w/w. Total in vitro drug release from the ocular films was attained within 15 min following first-order kinetics, showing higher apparent permeability (Papp) values across porcine corneas compared to the drug's solution. The fabricated films did not induce any ocular irritation as evidenced by both the hen's egg test on chorioallantoic membrane and the in vivo Draize test. In vivo administration of the ocular films in rabbits induced a faster onset of action and a sustained IOP-lowering effect up to 24 h compared to TM solution, suggesting that the proposed ocular films are promising systems for the sustained topical delivery of TM.
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