4.8 Article

Nucleic Acid-Gated Covalent Organic Frameworks for Cancer-Specific Imaging and Drug Release

Journal

ANALYTICAL CHEMISTRY
Volume 93, Issue 34, Pages 11751-11757

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c02105

Keywords

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Funding

  1. National Key RAMP
  2. D Program of China [2019YFA0210100]
  3. National Natural Science Foundation of China [21927811, 21874086, 21775094]
  4. Youth Innovation Science and Technology Program of Higher Education Institution of Shandong Province [2019KJC022]

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The rational design of a smart nucleic acid-gated COF nanosystem has enabled cancer-specific imaging and drug release, with the ability to release drugs and restore fluorescence signals in cancer cells. This work provides a promising nanoplatform for cancer theranostics and highlights the potential for regulating interactions between COFs and biomolecules.
Developing nanoplatforms that simultaneously integrate diagnostic imaging and therapy functions has been a promising but challenging task for cancer theranostics. Herein, we report the rational design of a smart nucleic acid-gated covalent organic framework (COF) nanosystem for cancer-specific imaging and microenvironment-responsive drug release. Cy5 dye-labeled single-stranded DNA (ssDNA) for mRNA recognition was adsorbed on the surface of doxorubicin (Dox)-loaded COF nanoparticles (NPs). Dox loaded in the pores of COF NPs could strengthen the interactions between ssDNA and COF and enhance the fluorescence quenching effect toward Cy5, while the densely coated ssDNA could prevent the leakage of Dox from COF NPs. The obtained nanosystem exhibited low fluorescence signal and Dox release in normal cells; however, the ssDNA could be released by the overexpressed TK1 mRNA in cancer cells to recover the intense fluorescence signal of Cy5, and the loaded Dox could be further released for chemotherapy. Therefore, cancer cell-specific diagnostic imaging and drug release were realized with the rationally developed nanosystem. This work offers a universal nanoplatform for cancer theranostics and a promising strategy for regulating the interaction between COFs and biomolecules.

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