TY - JOUR
T1 - A photoswitchable phase-reversible gel engine for systemic redox homeostasis remodeling and on-demand chemodynamic immunotherapy with sustainable immunostimulation
AU - Sun, Minghao
AU - Liu, Weiwei
AU - Ma, Yuanyuan
AU - Ni, Pengfei
AU - Yao, Wenjing
AU - Xu, Yingjie
AU - Bao, Rui
AU - Wang, Jue
AU - Xiong, Fei
AU - Kuang, Xihe
AU - Zhang, Teng
AU - Zhang, Xiaochen
AU - Yao, Xikuang
AU - Ju, Shenghong
AU - Fan, Wenpei
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/3/1
Y1 - 2025/3/1
N2 - Chemodynamic therapy (CDT) efficacy in the tumor microenvironment (TME) remains compromised. Inspired by the potential of fever-like heat to activate a redox-favorable microenvironment, mild photothermal therapy (mPTT) is expected to sensitize tumors to CDT, turning “redox-cold” tumors into “redox-hot” ones. Herein, an injectable gel engine (LMFT@SG-R) is meticulously constructed based on the co-encapsulation of R848 and β-lapachone (LAP)-loaded metal–organic framework-199 (MOF-199) within a lipidic gel reservoir with the unique ability of thermally reversible sol–gel phase transformation. With mPTT reprogramming TME, the custom-designed LMFT@SG-R can realize systemic redox homeostasis remodeling through mPTT-activated chemodynamic immunotherapy (MPCIT). Once reaching the TME, LMFT@SG-R quickly hydrates into solid gel and subsequently undergoes gel-to-sol transformation under mild NIR laser irradiation, resulting in on-demand release of LMFT and R848 for controllable CDT and immunostimulation. LMFT undergoes stepwise degradation for sequential release of Fe3+, Cu2+ and LAP, which can promote ROS cascade amplification owing to the upregulation of HSP70/NQO1 axis upon mild hyperthermia, resulting in robust ICD effects and T lymphocytes infiltrations together with R848. Notably, the controllable immunostimulation can facilitate robust abscopal effects and prominent suppression of distal tumors. The well-designed LMFT@SG-R may represent an updated CDT catalyst with the highly-integrated gel engine for chained-cooperative MPCIT.
AB - Chemodynamic therapy (CDT) efficacy in the tumor microenvironment (TME) remains compromised. Inspired by the potential of fever-like heat to activate a redox-favorable microenvironment, mild photothermal therapy (mPTT) is expected to sensitize tumors to CDT, turning “redox-cold” tumors into “redox-hot” ones. Herein, an injectable gel engine (LMFT@SG-R) is meticulously constructed based on the co-encapsulation of R848 and β-lapachone (LAP)-loaded metal–organic framework-199 (MOF-199) within a lipidic gel reservoir with the unique ability of thermally reversible sol–gel phase transformation. With mPTT reprogramming TME, the custom-designed LMFT@SG-R can realize systemic redox homeostasis remodeling through mPTT-activated chemodynamic immunotherapy (MPCIT). Once reaching the TME, LMFT@SG-R quickly hydrates into solid gel and subsequently undergoes gel-to-sol transformation under mild NIR laser irradiation, resulting in on-demand release of LMFT and R848 for controllable CDT and immunostimulation. LMFT undergoes stepwise degradation for sequential release of Fe3+, Cu2+ and LAP, which can promote ROS cascade amplification owing to the upregulation of HSP70/NQO1 axis upon mild hyperthermia, resulting in robust ICD effects and T lymphocytes infiltrations together with R848. Notably, the controllable immunostimulation can facilitate robust abscopal effects and prominent suppression of distal tumors. The well-designed LMFT@SG-R may represent an updated CDT catalyst with the highly-integrated gel engine for chained-cooperative MPCIT.
KW - Cascade ROS amplification
KW - Chemodynamic immunotherapy
KW - Reversible phase transition
KW - Sequential drug release
KW - Thermosensitive gel engine
UR - http://www.scopus.com/inward/record.url?scp=85217909914&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2025.160516
DO - 10.1016/j.cej.2025.160516
M3 - 文章
AN - SCOPUS:85217909914
SN - 1385-8947
VL - 507
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 160516
ER -