A novel liposomal formulation of FTY720 (Fingolimod) for promising enhanced targeted delivery
详细信息 查看全文
- 作者：Yicheng Mao ; Jiang Wang ; Yuan Zhao ; Yun Wu ; Kwang Joo Kwak ; Ching-Shih Chen ; John C. Byrd ; Robert J. Lee ; Mitch A. Phelps ; L. James Lee ; Natarajan Muthusamy
- 关键词：FTY720 ; Liposome ; Leukemia ; Drug delivery ; CD37 ; Nanotechnology
- 刊名：Nanomedicine: Nanotechnology, Biology and Medicine
- 出版年：February, 2014
- 年：2014
- 卷：10
- 期：2
- 页码：393-400
- 全文大小：1019 K
文摘
We describe here the development and characterization of the physicochemical and pharmacokinetic properties of a novel liposomal formulation for FTY720 delivery, LP-FTY720. The mean diameter of LP-FTY720 was ~ 157 nm, and the FTY720 entrapment efficiency was ~ 85%. The liposomal formulation protected FTY720 from degradation in aqueous buffer and showed toxicity in CLL patient B cells comparable to that of free FTY720. Following intravenous injection in ICR mice, LP-FTY720 had an increased elimination phase half-life (~ 28 vs. ~ 19 hr) and decreased clearance (235 vs. 778 mL/h/kg) compared to the free drug. Antibodies against CD19, CD20 and CD37 were incorporated into LP-FTY720, which provided targeted delivery to CLL patient B cells and thus achieved higher killing efficacy. The novel liposomal carrier of FTY720 demonstrated improved pharmacokinetic properties, comparable activity, and a potential platform for targeted delivery to CLL by overcoming the limited application of free FTY720 to B malignancy treatment.
From the Clinical Editor
This team reports on a novel liposomal formulation for FTY720 delivery, demonstrating improved pharmacokinetic properties, comparable activity, and a potential platform for targeted delivery to CLL using antibodies incorporated in the liposomes. The method expected to overcome the limited application of free FTY720 to B malignancy treatment.