Gómez-Ballesteros Miguel, López-Cano José Javier, Bravo-Osuna Irene, Herrero-Vanrell Rocío, Molina-Martínez Irene Teresa
Complutense University, Innovation, Therapy and Pharmaceutical Development in Ophthalmology (InnOftal) Research Group, UCM 920415, Department of Pharmaceutics and Food Technology, Faculty of Pharmacy, Plaza Ramón y Cajal s/n, Madrid 28040, Spain.
Ocular Pathology National Net (OFTARED) of the Institute of Health Carlos III, Health Research Institute of the San Carlos Clinical Hospital (IdISSC), Madrid 28040, Spain.
Polymers (Basel). 2019 May 28;11(6):929. doi: 10.3390/polym11060929.
The combination of acetazolamide-loaded nano-liposomes and Hydroxypropyl methylcellulose (HPMC) with similar components to the preocular tear film in an osmoprotectant media (trehalose and erythritol) is proposed as a novel strategy to increase the ocular bioavailability of poorly soluble drugs. Ophthalmic formulations based on acetazolamide-loaded liposomes, dispersed in the osmoprotectant solution (ACZ-LP) or in combination with HPMC (ACZ-LP-P) were characterized and in vivo evaluated. The pH and tonicity of both formulations resulted in physiological ranges. The inclusion of HPMC produced an increment in viscosity (from 0.9 to 4.7 mPa·s. 64.9 ± 2.6% of acetazolamide initially included in the formulation was retained in vesicles. In both formulations, a similar onset time (1 h) and effective time periods were observed (7 h) after a single instillation (25 μL) in normotensive rabbits' eyes. The AUC of the ACZ-LP-P was 1.5-fold higher than of ACZ-LP ( < 0.001) and the maximum hypotensive effect resulted in 1.4-fold higher ( < 0.001). In addition, the formulation of ACZ in the hybrid liposome/HPMC system produced a 30.25-folds total increment in ocular bioavailability, compared with the drug solution. Excellent tolerance in rabbits' eyes was confirmed during the study.
将载有乙酰唑胺的纳米脂质体与羟丙基甲基纤维素(HPMC)相结合,并添加与眼表泪膜成分相似的渗透保护剂(海藻糖和赤藓糖醇),被认为是一种提高难溶性药物眼部生物利用度的新策略。对基于载有乙酰唑胺的脂质体、分散于渗透保护剂溶液(ACZ-LP)或与HPMC联合使用(ACZ-LP-P)的眼科制剂进行了表征和体内评估。两种制剂的pH值和渗透压均在生理范围内。加入HPMC使粘度增加(从0.9至4.7 mPa·s)。制剂中最初包含的乙酰唑胺有64.9±2.6%保留在囊泡中。在正常血压兔眼中单次滴注(25μL)后,两种制剂观察到相似的起效时间(1小时)和有效时间段(7小时)。ACZ-LP-P的AUC比ACZ-LP高1.5倍(<0.001),最大降压效果高1.4倍(<0.001)。此外,与药物溶液相比,在脂质体/HPMC混合系统中配制的ACZ眼部生物利用度提高了30.25倍。研究期间证实兔眼具有良好的耐受性。