School of Pharmacy, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Yantai University, Yantai, Shandong Province, People's Republic of China; School of Pharmacy, Jining Medical University, Jining, Shandong Province, People's Republic of China.
School of Pharmacy, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Yantai University, Yantai, Shandong Province, People's Republic of China; State Key Laboratory of Long-Acting and Targeting Drug Delivery System, Shandong Luye Pharmaceutical Co., Ltd, Yantai, Shandong Province, People's Republic of China.
Int J Pharm. 2019 Apr 5;560:27-34. doi: 10.1016/j.ijpharm.2019.01.052. Epub 2019 Jan 31.
To avoid severe exacerbations in the load of hepatitis B virus (HBV) as a consequence of discontinuous use of anti-HBV drugs, entecavir (ETV), the first-line anti-HBV drug, was primally formulated as extended-release poly (lactic-co-glycolic acid) microspheres in the present study. Because ETV is slightly soluble in water and in some other organic solvents used for microsphere preparation, methods for solid-microencapsulation were employed to fabricate the ETV microspheres. The optimized microspheres were evaluated for their morphology, particle size, drug loading, in vitro drug release, and in vivo pharmacokinetics in rats. The optimized formulation was found to have a mean particle size of 86 µm and drug loading of 13%. Differential scanning calorimetry and powder X-ray diffraction indicated that ETV existed in crystal, amorphous, and molecular states in the microspheres. In vitro and in vivo release revealed that the dissolution of ETV dominated the release process. The morphology of the microspheres and changes in the morphology during in vitro release were assessed by scanning electron microscopy. The novel ETV-MS described in this study should have great potential for clinical use as an alternative treatment against HBV.
为避免因抗乙型肝炎病毒 (HBV) 药物间断使用而导致 HBV 载量急剧增加,本研究最初将一线抗 HBV 药物恩替卡韦(ETV)制成了聚乳酸-羟基乙酸共聚物(PLGA)的缓释微球。由于 ETV 在水中和一些用于微球制备的有机溶剂中的溶解度较低,因此采用固载微囊化方法来制备 ETV 微球。对优化后的微球的形态、粒径、载药量、体外药物释放和大鼠体内药代动力学进行了评价。优化后的配方的平均粒径为 86µm,载药量为 13%。差示扫描量热法和粉末 X 射线衍射表明,ETV 在微球中以晶体、无定形和分子状态存在。体外和体内释放表明,ETV 的溶解主导了释放过程。通过扫描电子显微镜评估了微球的形态和体外释放过程中形态的变化。本研究中描述的新型 ETV-MS 有望作为 HBV 的替代治疗方法在临床上得到广泛应用。