The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.
Conferring Ti‐Based MOFs with Defects for Enhanced Sonodynamic Cancer Therapy
Abstract
The development of highly efficient, multifunctional, and biocompatible sonosensitizer is still a priority for current sonodynamic therapy (SDT). Herein, a defect‐rich Ti‐based metal–organic framework (MOF) (D‐MOF(Ti)) with greatly improved sonosensitizing effect is simply constructed and used for enhanced SDT. Compared with the commonly used sonosensitizer TiO 2, D‐MOF(Ti) results in a superior reactive oxygen species (ROS) yield under ultrasound (US) irradiation due to its narrow bandgap, which principally improves the US‐triggered electron–hole separation. Meanwhile, due to the existence of Ti 3+ ions, D‐MOF(Ti) also exhibits a high level of Fenton‐like activity to enable chemodynamic therapy. Particularly, US as the excitation source of SDT can simultaneously enhance the Fenton‐like reaction to achieve remarkably synergistic outcomes for oncotherapy. More importantly, D‐MOF(Ti) can be degraded and metabolized out of the body after completion of its therapeutic functions without off‐target toxicity. Overall, this work identifies a novel Ti‐familial sonosensitizer harboring great potential for synergistic sonodynamic and chemodynamic cancer therapy.
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Cited by
Zhou, Y., Fan, S., Feng, L., Huang, X., & Chen, X. (2021) · Advanced Materials · doi:10.1002/adma.202104223 · Cited by 463
Nanoscale covalent organic frameworks: from controlled synthesis to cancer therapy
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Nano-ROS-generating approaches to cancer dynamic therapy: Lessons from nanoparticles
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Metadata
- Authors
- Liang, S., Xiao, X., Bai, L., Liu, B., Yuan, M., Ma, P., Pang, M., Cheng, Z., & Lin, J.
- Venue
- Advanced Materials
- Publisher
- Wiley
- Published
- 2021-04
- Volume
- 33
- Issue
- 18
- Pages
- e2100333-e2100333
- ISSN
- 0935-9648 (ISSN-L)
- 1521-4095
- OpenAlex
- W3148405623
- Cited by
- 359
- References
- 52
- FWCI
- 17.85
- Type
- journal article
- Language
- en
- Open access
- closed
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