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- Publisher Website: 10.1021/acs.nanolett.5c01632
- Scopus: eid_2-s2.0-105003587699
- PMID: 40219956
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Article: Jahn-Teller-Driven Electronic Modulation of Bio-Heterojunction for Wound Regeneration after Postoperative Tumor Resection
| Title | Jahn-Teller-Driven Electronic Modulation of Bio-Heterojunction for Wound Regeneration after Postoperative Tumor Resection |
|---|---|
| Authors | |
| Keywords | Antibacterial Antitumor Bioheterojunction Tissue regeneration |
| Issue Date | 23-Apr-2025 |
| Publisher | American Chemical Society |
| Citation | Nano Letters, 2025, v. 25, n. 16, p. 6828-6838 How to Cite? |
| Abstract | Abundant ·OH, 1O2, and ·O2- provide an efficient methodology for rapid tumor and bacteria killing, whereas a limitation focuses on the catalytic efficiency. Thus, Jahn-Teller-driven electronic modulation of a bioheterojunction (bioHJ) platform is developed for the remedy in diabetic infectious wound regeneration after postoperative tumor resection. The bioHJ is composed of MoTe2/MnO2 and glucose oxidase (GOx). GOx depletes glucose to H2O2, which intercepts their glucose metabolism. The H2O2 can be further converted into highly lethal ·OH owing to peroxidase-mimetic activity via the Jahn-Teller effect, while GSH can be consumed due to its GPx-mimetic activity. Both of which can be further amplified upon NIR irradiation as NIR-activatable enzyme-mimetic activities. In vivo studies in a subcutaneous tumor model and infectious model authenticate the ability to kill tumor, defeat bacterial infection, and accelerate wound regeneration. This work enlightens a powerful platform for postoperative infectious wound regeneration of tumor resection using an engineered bioHJ. |
| Persistent Identifier | http://hdl.handle.net/10722/359245 |
| ISSN | 2023 Impact Factor: 9.6 2023 SCImago Journal Rankings: 3.411 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | He, Miaomiao | - |
| dc.contributor.author | Yang, Xuyang | - |
| dc.contributor.author | Xiang, Danni | - |
| dc.contributor.author | Chan, Yau Kei | - |
| dc.contributor.author | Yin, Guangfu | - |
| dc.contributor.author | Yang, Weizhong | - |
| dc.contributor.author | Deng, Yi | - |
| dc.date.accessioned | 2025-08-26T00:30:22Z | - |
| dc.date.available | 2025-08-26T00:30:22Z | - |
| dc.date.issued | 2025-04-23 | - |
| dc.identifier.citation | Nano Letters, 2025, v. 25, n. 16, p. 6828-6838 | - |
| dc.identifier.issn | 1530-6984 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/359245 | - |
| dc.description.abstract | <p>Abundant ·OH, <sup>1</sup>O2, and ·O2<sup>-</sup> provide an efficient methodology for rapid tumor and bacteria killing, whereas a limitation focuses on the catalytic efficiency. Thus, Jahn-Teller-driven electronic modulation of a bioheterojunction (bioHJ) platform is developed for the remedy in diabetic infectious wound regeneration after postoperative tumor resection. The bioHJ is composed of MoTe2/MnO2 and glucose oxidase (GOx). GOx depletes glucose to H2O2, which intercepts their glucose metabolism. The H2O2 can be further converted into highly lethal ·OH owing to peroxidase-mimetic activity via the Jahn-Teller effect, while GSH can be consumed due to its GPx-mimetic activity. Both of which can be further amplified upon NIR irradiation as NIR-activatable enzyme-mimetic activities. In vivo studies in a subcutaneous tumor model and infectious model authenticate the ability to kill tumor, defeat bacterial infection, and accelerate wound regeneration. This work enlightens a powerful platform for postoperative infectious wound regeneration of tumor resection using an engineered bioHJ.</p> | - |
| dc.language | eng | - |
| dc.publisher | American Chemical Society | - |
| dc.relation.ispartof | Nano Letters | - |
| dc.subject | Antibacterial | - |
| dc.subject | Antitumor | - |
| dc.subject | Bioheterojunction | - |
| dc.subject | Tissue regeneration | - |
| dc.title | Jahn-Teller-Driven Electronic Modulation of Bio-Heterojunction for Wound Regeneration after Postoperative Tumor Resection | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1021/acs.nanolett.5c01632 | - |
| dc.identifier.pmid | 40219956 | - |
| dc.identifier.scopus | eid_2-s2.0-105003587699 | - |
| dc.identifier.volume | 25 | - |
| dc.identifier.issue | 16 | - |
| dc.identifier.spage | 6828 | - |
| dc.identifier.epage | 6838 | - |
| dc.identifier.eissn | 1530-6992 | - |
| dc.identifier.issnl | 1530-6984 | - |
