Delivery of rapamycin to dendritic cells using degradable microparticles

作者：Jhunjhunwala S; Raimondi G; Thomson A W; Little S R^*

来源：Journal of Controlled Release, 2009, 133(3): 191-197.

DOI：10.1016/j.jconrel.2008.10.011

• Microparticles
• PLGA
• Rapamycin
• Dendritic cells
• Intracellular delivery

Degradable microparticles have the potential to protect and release drugs over extended periods and, if sized appropriately, can be passively targeted to phagocytic cells in vivo. Dendritic cells (DC) are a class of phagocytic cells known to play important roles in transplant rejection. Previously, we have demonstrated that DC treated with an immunosuppressive drug, rapamycin, have the ability to suppress transplant rejection. Herein, we describe a strategy to deliver an intracellular depot of rapamycin to DC. To achieve this, rapamycin was encapsulated into similar to 3.4 mu m sized poly(lactic-co-glycolic)acid (PLGA) microparticles (rapaMPs), and release behavior was examined under intra-phagosomal (pH = 5) and extracellular (pH = 7.4) conditions. It was observed that 4 days following phagocytosis of rapaMP, DC have significantly reduced ability to activate T cells, in comparison to DC treated with soluble rapamycin. Hence, we conclude that DC-specific intracellular delivery of rapamycin results in better efficacy of the drug, with respect to its ability to modulate DC function, when compared to treating DC with extracellular rapamycin.

• 出版日期2009-2-10