González-Cela-Casamayor Miriam Ana, López-Cano José Javier, Bravo-Osuna Irene, Andrés-Guerrero Vanessa, Vicario-de-la-Torre Marta, Guzmán-Navarro Manuel, Benítez-Del-Castillo José Manuel, Herrero-Vanrell Rocío, Molina-Martínez Irene Teresa
Innovation, Therapy and Pharmaceutical Development in Ophthalmology (InnOftal) Research Group, Universidad Complutense de Madrid (UCM), 28040 Madrid, Spain.
Department of Pharmaceutics and Food Technology, Facultad de Farmacia, Universidad Complutense de Madrid (UCM), IdISSC, 28040 Madrid, Spain.
Pharmaceutics. 2022 Jul 4;14(7):1405. doi: 10.3390/pharmaceutics14071405.
Glaucoma is a group of chronic irreversible neuropathies that affect the retina and the optic nerve. It is considered one of the leading causes of blindness in the world. Although it can be due to various causes, the most important modifiable risk factor is the elevated intraocular pressure (IOP). In this case, the treatment of choice consists of instilling antihypertensive formulations on the ocular surface. The chronicity of the pathology, together with the low bioavailability of the drugs that are applied on the ocular surface, make it necessary to instill the formulations very frequently, which is associated, in many cases, with the appearance of dry eye disease (DED). The objective of this work is the design of topical ocular formulations capable of treating glaucoma and, at the same time, preventing DED. For this, two liposome formulations, loaded with brimonidine or with travoprost, were Tadeveloped using synthetic phospholipids and enriched by the addition of compounds with osmoprotective activity. The proposed formulations not only presented physicochemical characteristics (size, pH, osmolarity, surface tension, and viscosity) and encapsulation efficiency values (EE% of 24.78% and ≥99.01% for brimonidine and travoprost, respectively) suitable for ocular surface administration, but also showed good tolerance in human corneal and conjunctival cell cultures, as well as an in vitro osmoprotective activity. The hypotensive effect of both liposomal formulations was evaluated in normotensive albino New Zealand rabbits, showing a faster and longer lasting reduction of intraocular pressure in comparison to the corresponding commercialized products used as control. According to these results, the hypotensive liposomal formulations combined with osmoprotective agents would result in a very promising platform for the treatment of glaucoma and the simultaneous protection of the ocular surface.
青光眼是一组影响视网膜和视神经的慢性不可逆性神经病变。它被认为是全球失明的主要原因之一。尽管其病因多样,但最重要的可改变风险因素是眼压升高(IOP)。在这种情况下,首选的治疗方法是在眼表滴注抗高血压制剂。该疾病的慢性性质,加上眼表用药的低生物利用度,使得必须非常频繁地滴注制剂,这在许多情况下与干眼症(DED)的出现有关。这项工作的目的是设计能够治疗青光眼并同时预防干眼症的局部眼用制剂。为此,使用合成磷脂开发了两种分别载有溴莫尼定或曲伏前列素的脂质体制剂,并通过添加具有渗透保护活性的化合物进行富集。所提出的制剂不仅呈现出适合眼表给药的物理化学特性(大小、pH值、渗透压、表面张力和粘度)和包封效率值(溴莫尼定和曲伏前列素的包封率分别为24.78%和≥99.01%),而且在人角膜和结膜细胞培养中显示出良好的耐受性以及体外渗透保护活性。在正常血压的新西兰白化兔中评估了两种脂质体制剂的降压效果,结果表明与用作对照的相应商业化产品相比,眼压降低更快且持续时间更长。根据这些结果,与渗透保护剂结合的降压脂质体制剂将成为治疗青光眼和同时保护眼表的非常有前景的平台。