Mesoporous Silica Nanoparticles with pH-Sensitive Nanovalves for Delivery of Moxifloxacin Provide Improved Treatment of Lethal Pneumonic Tularemia
journal contributionposted on 24.11.2015, 00:00 by Zilu Li, Daniel L. Clemens, Bai-Yu Lee, Barbara Jane Dillon, Marcus A. Horwitz, Jeffrey I. Zink
We have optimized mesoporous silica nanoparticles (MSNs) functionalized with pH-sensitive nanovalves for the delivery of the broad spectrum fluoroquinolone moxifloxacin (MXF) and demonstrated its efficacy in treating Francisella tularensis infections both in vitro and in vivo. We compared two different nanovalve systems, positive and negative charge modifications of the mesopores, and different loading conditionsvarying pH, cargo concentration, and duration of loading–and identified conditions that maximize both the uptake and release capacity of MXF by MSNs. We have demonstrated in macrophage cell culture that the MSN-MXF delivery platform is highly effective in killing F. tularensis in infected macrophages, and in a mouse model of lethal pneumonic tularemia, we have shown that the drug-loaded MSNs are much more effective in killing F. tularensis than an equivalent amount of free MXF.
Read the peer-reviewed publication
pneumonic tularemiaMSNnanovalve systemsspectrum fluoroquinolone moxifloxacinMesoporous Silica Nanoparticlesloadingequivalent amountcargo concentrationFrancisella tularensis infectionsMXFcharge modificationsoptimized mesoporous silica nanoparticlesrelease capacitymacrophage cell culturemouse modelLethal Pneumonic TularemiaWe