Long Danhong, Gong Tao, Zhang Zhirong, Ding Rui, Fu Yao
Key Laboratory of Drug Targeting and Drug Delivery Systems, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.
Beijing Institute for Drug Control, Beijing 100035, China.
Acta Pharm Sin B. 2016 Jul;6(4):329-35. doi: 10.1016/j.apsb.2016.05.004. Epub 2016 Jun 16.
A phospholipid-based injectable gel was developed for the sustained delivery of leuprolide acetate (LA). The gel system was prepared using biocompatible materials (SPME), including soya phosphatidyl choline (SPC), medium chain triglyceride (MCT) and ethanol. The system displayed a sol state with low viscosity in vitro and underwent in situ gelation in vivo after subcutaneous injection. An in vitro release study was performed using a dialysis setup with different release media containing different percentages of ethanol. The stability of LA in the SPME system was investigated under different temperatures and in the presence of various antioxidants. In vivo studies in male rats were performed to elucidate the pharmacokinetic profiles and pharmacodynamic efficacy. A sustained release of LA for 28 days was observed without obvious initial burst in vivo. The pharmacodynamic study showed that once-a-month injection of LA-loaded SPME (SPME-LA) led to comparable suppression effects on the serum testosterone level as observed in LA solution except for the onset time. These findings demonstrate excellent potential for this novel SPME system as a sustained release delivery system for LA.
一种基于磷脂的可注射凝胶被开发用于醋酸亮丙瑞林(LA)的持续递送。该凝胶系统使用生物相容性材料(SPME)制备,包括大豆磷脂酰胆碱(SPC)、中链甘油三酯(MCT)和乙醇。该系统在体外呈现低粘度的溶胶状态,皮下注射后在体内发生原位凝胶化。使用含有不同乙醇百分比的不同释放介质的透析装置进行了体外释放研究。在不同温度和各种抗氧化剂存在的情况下,研究了LA在SPME系统中的稳定性。在雄性大鼠中进行了体内研究,以阐明药代动力学特征和药效学功效。在体内观察到LA持续释放28天,且无明显的初始突释。药效学研究表明,每月一次注射载有LA的SPME(SPME-LA)对血清睾酮水平的抑制作用与LA溶液相当,只是起效时间有所不同。这些发现证明了这种新型SPME系统作为LA持续释放递送系统具有巨大潜力。