Versatile Fluorescence Resonance Energy Transfer-Based Mesoporous Silica Nanoparticles for Real-Time Monitoring of Drug Release

We describe the development of a versatile fluorescence resonance energy transfer (FRET)-based real-time monitoring system, consisting of (a) coumarinlabeled-cysteine tethered mesoporous silica nanoparticies (MSNs) as the drug carrier, (b) a fluorescein isothlocyanate-fi-cyclodextrin (FITC-f3-(D) as redoxresponsive molecular valve blocking the pores, and (c) a FRET donor acceptor pair of coumarin and FITC integrated within the pore-unlocking event, thereby allowing for monitoring the release of drugs from the pores in real-time. Under nonreducing conditions, when the disulfide bond Is intact, the close proximity between coumarin and FITC on the surface of MSNs results in FRET from coumarin to FIR. However, in the presence of the redox stimuli like giutathione (GSH), the disulfide bond is deaved which leads to the removal of molecular valve (FITC-fi-(D), thus triggering drug release and eliminating FRET. By engineering such a FRET-active donor acceptor structure within the redox-responsive molecular valve, we can monitor the release of the drugs entrapped within the pores of the MSN nanocarrier, following the change In the FRET signal. We have demonstrated that, any exogenous or endogenous change in the GSH concentration will result in a change in the extent of drug release as well as a concurrent change in the FRET signal, allowing us to extend the applications of our FRET-based MSNs for monitoring the release of any type of drug molecule in real-time.