Oxygen self-enriched single-component "black carbon nitride" for near-infrared phototheranostics
Single component agent-based near-infrared phototheranostics has captivated researchers in cancer treatment over recent decades. However, the current single-component agents rarely alleviate the hypoxic microenvironment in tumor cells, which severely limits the development of photodynamic therapy. H...
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Published in | Nanoscale Vol. 12; no. 42; pp. 21812 - 2182 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
05.11.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Single component agent-based near-infrared phototheranostics has captivated researchers in cancer treatment over recent decades. However, the current single-component agents rarely alleviate the hypoxic microenvironment in tumor cells, which severely limits the development of photodynamic therapy. Here, we report a new phototheranostic agent, single-component black graphite carbon nitride nanoparticles (named CN-B NPs), synthesized through thermal copolymerization. Compared with unmodified graphitic carbon nitride (g-C
3
N
4
), the absorption of CN-B NPs in the near-infrared region was enhanced. Through
in vitro
and
in vivo
studies, we demonstrated that CN-B NPs can be used as a near-infrared phototheranostic agent in both normoxia and hypoxia, simultaneously allowing infrared thermal/photoacoustic imaging and photodynamic/photothermal co-therapy, thereby resulting in remarkable inhibition of tumor growth. This approach could provide a new method to achieve multimodal phototheranostics using a single-component material.
Single component agent-based near-infrared phototheranostics has captivated researchers in cancer treatment over recent decades. |
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Bibliography: | 10.1039/d0nr05871h Electronic supplementary information (ESI) available. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2040-3364 2040-3372 2040-3372 |
DOI: | 10.1039/d0nr05871h |