Preparation of 2D Polyaniline/MoO 3- x Superlattice Nanosheets via Intercalation-Induced Morphological Transformation for Efficient Chemodynamic Therapy
Organic intercalation of layered nanomaterials is an attractive strategy to fabricate organic/inorganic superlattices for a wide range of promising applications. However, the synthesis of 2D organic/inorganic superlattice nanosheets remains a big challenge. Herein, the preparation of 2D polyaniline/...
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Veröffentlicht in: | Advanced healthcare materials 2023-04, Vol.12 (11), p.e2202911 |
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Sprache: | eng |
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Zusammenfassung: | Organic intercalation of layered nanomaterials is an attractive strategy to fabricate organic/inorganic superlattices for a wide range of promising applications. However, the synthesis of 2D organic/inorganic superlattice nanosheets remains a big challenge. Herein, the preparation of 2D polyaniline/MoO
(PANI/MoO
) superlattice nanosheets via intercalation-induced morphological transformation from MoO
nanobelts, as efficient Fenton-like reagents for chemodynamic therapy (CDT), is reported. Micrometer-long MoO
nanobelts are co-intercalated with Na
/H
O followed by the guest exchange with aniline monomer for in situ polymerization to obtain PANI/MoO
nanosheets. Intriguingly, the PANI intercalation can induce the morphological transformation from long MoO
nanobelts to 2D PANI/MoO
nanosheets along with the partial reduction of Mo
to Mo
, and generation of rich oxygen vacancies. More importantly, thanks to the PANI intercalation-induced activation, the PANI/MoO
nanosheets exhibit excellent Fenton-like catalytic activity for generation of hydroxyl radical (·OH) by decomposing H
O
compared with the MoO
nanobelts. It is speculated that the good conductivity of PANI can facilitate electron transport during the Fenton-like reaction, thereby enhancing the efficiency of CDT. Thus, the polyvinylpyrrolidone-modified PANI/MoO
nanosheets can function as Fenton-like reagents for highly efficient CDT to kill cancer cells and eradicate tumors. |
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ISSN: | 2192-2640 2192-2659 |
DOI: | 10.1002/adhm.202202911 |