Laboratory of Pharmaceutical Technology, Department of Pharmacy, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki GR 54124, Greece.
Comparative Ophthalmology Unit, Department of Clinical Studies, School of Veterinary Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki GR 54627, Greece.
Mol Pharm. 2022 Jan 3;19(1):274-286. doi: 10.1021/acs.molpharmaceut.1c00766. Epub 2021 Dec 8.
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 () 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.
用于治疗青光眼的最常见的眼压(IOP)降低方案包括局部使用眼药水,这种剂型在作用部位的停留时间短,剂量增加频率高,患者顺应性降低。通过静电纺丝制备了包含聚乙烯醇和泊洛沙姆 407 的原位凝胶纳米纤维膜,用于马来酸噻吗洛尔(TM)的眼部给药,旨在与传统眼药水相比,维持β受体阻滞剂的降眼压作用。对静电纺丝工艺进行了优化,并对所开发配方的理化性质进行了深入研究。载药薄膜的纤维直径在 123 至 145nm 之间,药物含量在 5.85%至 7.83%w/w 之间。药物从眼部薄膜中的总体外释放在 15 分钟内达到一级动力学,与药物溶液相比,在猪角膜上显示出更高的表观渗透()值。所制备的薄膜没有引起任何眼部刺激,这一点可以通过鸡胚绒毛尿囊膜的鸡蛋试验和体内 Draize 试验得到证明。与 TM 溶液相比,兔眼内给药后,眼部薄膜能更快地发挥作用,并能持续降低眼压长达 24 小时,这表明所提出的眼部薄膜是 TM 持续局部递送的有前途的系统。