TY - JOUR
T1 - A photosensitive sustainable lignin nanoplatform for multimodal image-guided mitochondria-targeted photodynamic and photothermal therapy
AU - Liu, X.
AU - Li, M.
AU - Li, X.
AU - Ge, M.
AU - Liu, S.
AU - Li, S.
AU - Li, J.
AU - Ding, J.
AU - Ragauskas, A. J.
AU - Sun, W.
AU - James, T. D.
AU - Chen, Z.
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China ( 31890774 and 31800494 ), Natural Science Funding of Heilong Jiang province for Excellent Young Scholar (YQ2020C017). TDJ wishes to thank the Royal Society for a Wolfson Research Merit Award and the Open Research Fund of the School of Chemistry and Chemical Engineering, Henan Normal University for support (2020ZD01).
PY - 2022/12/31
Y1 - 2022/12/31
N2 - Photoactivated nanocarriers exhibit significant potential for anticancer therapy, but complex design strategies, unsustainable substrates, and short wavelengths limit their practical application. Here, we designed a new lignin-derived photoactivated nanomaterial that exploits the sensitivity of the β-O-4 bond of lignin to singlet oxygen. This sustainable product was loaded with mitochondria-targeting chlorin e6 and black phosphorus quantum dots (BPQDs) to produce BPQDs@N-LgC NPs, which were used for mitochondria-targeted fluorescence/photoacoustic-guided photothermal and photodynamic therapy. When irradiated at 808 nm, the BPQDs in BPQDs@N-LgC NPs exhibited good photothermal conversion, which allowed photoacoustic imaging and inhibited tumor growth. When irradiated at 660 nm, the BPQDs@N-LgC NPs generated fluorescence and reactive oxygen species, which allowed photoluminescence imaging and further inhibited tumor growth. Cleavage of the β-O-4 bond of lignin by photo-triggered reactive oxygen species degraded the NPs and released the BPQDs, facilitating rapid excretion of the therapeutic nanomaterials. Our rationally designed BPQDs@N-LgC NPs exhibited good therapeutic efficacy, both in vitro and in vivo.
AB - Photoactivated nanocarriers exhibit significant potential for anticancer therapy, but complex design strategies, unsustainable substrates, and short wavelengths limit their practical application. Here, we designed a new lignin-derived photoactivated nanomaterial that exploits the sensitivity of the β-O-4 bond of lignin to singlet oxygen. This sustainable product was loaded with mitochondria-targeting chlorin e6 and black phosphorus quantum dots (BPQDs) to produce BPQDs@N-LgC NPs, which were used for mitochondria-targeted fluorescence/photoacoustic-guided photothermal and photodynamic therapy. When irradiated at 808 nm, the BPQDs in BPQDs@N-LgC NPs exhibited good photothermal conversion, which allowed photoacoustic imaging and inhibited tumor growth. When irradiated at 660 nm, the BPQDs@N-LgC NPs generated fluorescence and reactive oxygen species, which allowed photoluminescence imaging and further inhibited tumor growth. Cleavage of the β-O-4 bond of lignin by photo-triggered reactive oxygen species degraded the NPs and released the BPQDs, facilitating rapid excretion of the therapeutic nanomaterials. Our rationally designed BPQDs@N-LgC NPs exhibited good therapeutic efficacy, both in vitro and in vivo.
KW - Multimodal imaging
KW - Photodynamic and photothermal synergistic therapy
KW - Photosensitive lignin nanoplatform
KW - reactive oxygen species
UR - http://www.scopus.com/inward/record.url?scp=85133685381&partnerID=8YFLogxK
U2 - 10.1016/j.mtchem.2022.101000
DO - 10.1016/j.mtchem.2022.101000
M3 - Article
AN - SCOPUS:85133685381
SN - 2468-5194
VL - 26
JO - Materials Today Chemistry
JF - Materials Today Chemistry
M1 - 101000
ER -