Reversible stimuli-responsive controlled release using mesoporous silica nanoparticles functionalized with a smart DNA molecule-gated switch
We reported a novel reversible stimuli-responsive controlled-release system consisting of mesoporous silica nanoparticles (MSN) functionalized with a smart DNA molecule-gated switch. In this system, a unique sequential cytosine (C)-rich DNA as the smart molecule-gated switch was grafted on the mesop...
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Veröffentlicht in: | Journal of materials chemistry 2012-07, Vol.22 (29), p.14715-14721 |
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Sprache: | eng |
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Zusammenfassung: | We reported a novel reversible stimuli-responsive controlled-release system consisting of mesoporous silica nanoparticles (MSN) functionalized with a smart DNA molecule-gated switch. In this system, a unique sequential cytosine (C)-rich DNA as the smart molecule-gated switch was grafted on the mesoporous silica nanoparticles (MSN) surface. In the presence of Ag super(+) ions, the closer C-rich DNA could hybridize each other by the formation of C-Ag super(+)-C structure based on metal-dependent pairs of two nucleobases, resulting in blocking of pores and packing of guest molecules. By a competitive displacement reaction, the duplex DNA with C-Ag super(+)-C structure deformed into single-stranded DNA in the presence of thiol-containing molecules, such as dithiothreitol (DTT), which gave rise to uncapping and the subsequent release of the entrapped guest molecules. The reversible open and closed states of the DNA molecule-gated switch could be easily achieved by alternating addition of Ag super(+) linkers and DTT molecules. Our results demonstrated that the system had excellent loading amount (43 mu mol g super(-1)) and good controlled release behavior. Moreover, the system could enter the cells through endocytosis and showed a low cytotoxicity even with treatment at a high concentration (200 mu g mL super(-1)). We believe that the stimuli-responsive controlled MSN release system based on the smart molecule-gated switch could play an important role in the development intracellular delivery nanodevices. |
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ISSN: | 0959-9428 1364-5501 |
DOI: | 10.1039/c2jm32185h |