1. Bimetallic DNAsome Decorated with G 4 -DNA as a Nanozyme for Targeted and Enhanced Chemo/Chemodynamic Cancer Therapy.
- Author
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Raj G, Vasantha AP, Sreekumar VD, Beena AV, Dommeti VKK, Perozhy H, Jose AT, Khurana S, and Varghese R
- Subjects
- Humans, HeLa Cells, Animals, Neoplasms drug therapy, Neoplasms metabolism, G-Quadruplexes drug effects, Mice, Copper chemistry, Tumor Microenvironment drug effects, Mice, Nude, Doxorubicin chemistry, Doxorubicin pharmacology, DNA, Catalytic chemistry, DNA, Catalytic metabolism
- Abstract
Cancer is indisputably one of the major threats to mankind, and hence the design of new approaches for the improvement of existing therapeutic strategies is always wanted. Herein, the design of a tumor microenvironment-responsive, DNA-based chemodynamic therapy (CDT) nanoagent with dual Fenton reaction centers for targeted cancer therapy is reported. Self-assembly of DNA amphiphile containing copper complex as the hydrophobic Fenton reaction center results in the formation of CDT-active DNAsome with Cu
2+ -based Fenton catalytic site as the hydrophobic core and hydrophilic ssDNA protrude on the surface. DNA-based surface addressability of the DNAsome is then used for the integration of second Fenton reaction center, which is a peroxidase-mimicking DNAzyme noncovalently loaded with Hemin and Doxorubicin, via DNA hybridization to give a CDT agent having dual Fenton reaction centers. Targeted internalization of the CDT nanoagent and selective generation of• OH inside HeLa cell are also shown. Excellent therapeutic efficiency is observed for the CDT nanoagent both in vitro and in vivo, and the enhanced efficacy is attributed to the combined and synergetic action of CDT and chemotherapy., (© 2024 Wiley‐VCH GmbH.)- Published
- 2024
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