Skip to main content
. Author manuscript; available in PMC: 2020 Jan 1.
Published in final edited form as: Drug Discov Today. 2018 Oct 5;24(1):129–147. doi: 10.1016/j.drudis.2018.09.019

Figure 5.

Figure 5.

Schematic illustration of mercuric-ion-triggered drug release from mesoporous silica nanoparticles (MSNs) that were capped by dsDNA. The hydroxy functional groups on the surfaces of the MSNs were first conjugated to the isocyanate groups (-NCO) of 3(triethoxysilyl)propyl isocyanate (MSN-NCO). After model drug rhodamine 6G dye was loaded into the MSNs (MSN-R6G), the -NCO groups were conjugated with aminomodified two-arm-DNA strands [MSN (uncapped)]. The arm-DNA strands were further hybridized by a linker DNA to cap the dye-loaded MSNs [MSN (capped)]. Upon exposure to Hg2+ ions, the DNA strands underwent dehybridization and released the loaded dye [MSN (after cleavage of linker DNA)]. Adapted, with permission, from [58].