Department of Pharmacology, Instituto de Ciências Biomédicas - Universidade de Sao Paulo, Brazil.
Department of Pharmacology, Instituto de Ciências Biomédicas - Universidade de Sao Paulo, Brazil.
Int J Pharm. 2020 Jul 30;585:119474. doi: 10.1016/j.ijpharm.2020.119474. Epub 2020 May 27.
In this study, microemulsions capable of transforming into nanostructured hexagonal phase gels in vivo upon uptake of biological fluids for naltrexone prolonged release were investigated as a strategy for management of alcohol use disorder (AUD). Microemulsions were prepared using monoolein, tricaprylin, water and propylene glycol; after preliminary characterization, one formulation was selected, which contained 55% of monoolein-tricaprylin (M-55). This microemulsion displayed size below 200 nm and Newtonian rheological behavior. Liquid crystalline gels formed in vitro upon 8 h of contact with water following a second order kinetics. After 120 h, <50% of naltrexone was released in vitro independently on drug loading (5 or 10%). In vivo, gels formed within 24 h of M-55 subcutaneous administration, and persisted locally for over 30 days providing slow release of the fluorescent marker Alexa fluor compared to a solution. Using the conditioned place preference paradigm, a test used to measure drug's rewarding effects, a single dose of M-55 containing 5% naltrexone reduced the time spent in the ethanol-paired compartment by 1.8-fold compared to saline; this effect was similar to that obtained with daily naltrexone injections, demonstrating the formulation efficacy and its ability to reduce dosing frequency. A more robust effect was observed following administration of M-55 containing 10% of naltrexone, which was compatible with aversion. These results support M-55 as a platform for sustained release of drugs that can be further explored for management of AUD to reduce dosing frequency and aid treatment adherence.
在这项研究中,研究了能够在吸收生物体液后转化为体内纳米结构六方相凝胶的微乳液,作为管理酒精使用障碍(AUD)的一种策略。微乳液是使用单油酸甘油酯、三辛酸甘油酯、水和丙二醇制备的;经过初步表征,选择了一种含有 55%单油酸甘油酯-三辛酸甘油酯(M-55)的配方。这种微乳液显示出小于 200nm 的粒径和牛顿流变行为。在与水接触 8 小时后,以二级动力学形成体外液晶凝胶。120 小时后,体外释放的纳曲酮<50%,与药物载药量(5%或 10%)无关。在体内,M-55 皮下给药后 24 小时内形成凝胶,并在局部持续超过 30 天,与溶液相比,缓慢释放荧光标记物 Alexa fluor。使用条件性位置偏好范式,一种用于测量药物奖赏效应的测试,单次给予含有 5%纳曲酮的 M-55 可使在乙醇配对隔间中花费的时间减少 1.8 倍,与生理盐水相比;与每日纳曲酮注射获得的效果相似,证明了配方的疗效及其降低给药频率的能力。给予含有 10%纳曲酮的 M-55 可观察到更强的效果,这与厌恶感一致。这些结果支持 M-55 作为一种药物持续释放的平台,可以进一步探索用于管理 AUD,以降低给药频率并帮助治疗依从性。