Losa C, Alonso M J, Vila J L, Orallo F, Martinez J, Saavedra J A, Pastor J C
Laboratorio de Farmacia Galénica, Facultad de Farmacia, Santiago de Compostela, Spain.
J Ocul Pharmacol. 1992 Fall;8(3):191-8. doi: 10.1089/jop.1992.8.191.
A new formulation of metipranolol base for ophthalmic administration was developed consisting of a colloidal suspension of polyepsiloncaprolactone nanocapsules with an oily core (Migliol 840) in which the drug is dissolved. Physicochemical properties of the nanocapsules show that the polymer coating around the oily droplets causes an important reduction of the droplet size, with no significant modification of the surface charge noted. When this formulation was administered to rabbits, a reduction of intraocular pressure similar to that seen with commercial eye drops was observed. Nevertheless, the evaluation of the cardiovascular side effects clearly showed lower conjunctival absorption of the encapsulated drug compared with the commercial drops. The direct (bradycardia) and the indirect evaluation (based on the study of the influence on the hypotensive and positive chronotropic effects of isoprenaline) showed that blockage of beta-adrenoreceptors was reduced greatly by the topical administration of the new formulation.
研发出了一种用于眼部给药的甲吲洛尔碱新制剂,其由聚己内酯纳米囊的胶体悬浮液组成,纳米囊具有含油核心(Miglyol 840),药物溶解于该含油核心中。纳米囊的物理化学性质表明,油滴周围的聚合物包衣使油滴尺寸显著减小,而表面电荷无明显改变。当将该制剂给予兔子时,观察到眼压降低,与市售滴眼液相似。然而,心血管副作用评估清楚地表明,与市售滴眼液相比,包封药物的结膜吸收较低。直接评估(心动过缓)和间接评估(基于对异丙肾上腺素降压和正性变时作用影响的研究)表明,局部应用新制剂可大大降低β-肾上腺素受体的阻滞作用。