4.8 Article

A Drug-Self-Gated Mesoporous Antitumor Nanoplatform Based on pH-Sensitive Dynamic Covalent Bond

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 27, Issue 11, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201605985

Keywords

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Funding

  1. National Natural Science Foundation of China [21574091, 21576120, 31570978, 51373112]
  2. Guangdong Natural Science Funds [2014A030306036]
  3. Science and Technology Planning Project of Guangdong Province [2016A020217001]
  4. Natural Science Foundation of Guangdong Province [2015A030313848, 2016A030310023]
  5. Natural Science Foundation of Jiangsu Province [BK20160056, BK20150433, BK20140323]
  6. Innovation Commission of Shenzhen Municipality [JCYJ20160301152300347, JCYJ20150430163009479, JCYJ20150529164918738]

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To achieve on-demand drug release, mesoporous silica nanocarriers as antitumor platforms generally need to be gated with stimuli-responsive capping agents. Herein, a smart mesoporous nanocarrier that is gated by the drug itself through a pH-sensitive dynamic benzoic-imine covalent bond is demonstrated. The new system, which tactfully bypasses the use of auxiliary capping agents, could also exhibit desirable drug release at tumor tissues/cells and enhanced tumor inhibition. Moreover, a facile dynamic PEGylation via benzoic-imine bond further endows the drug-self-gated nanocarrier with tumor extracellular pH-triggered cell uptake and improves therapeutic efficiency in vivo. In short, the paradigm shift in capping agents here will simplify mesoporous nanomaterials as intelligent drug carriers for cancer therapy. Moreover, the self-gated strategy in this work also shows general potential for self-controlled delivery of natural biomolecules, for example, DNA/RNA, peptides, and proteins, due to their intrinsic amino groups.

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