A Hybrid Supramolecular Polymeric Nanomedicine for Cascade-Amplified Synergetic Cancer Therapy.
Kai YangShaolong QiXinyang YuBing BaiXueyan ZhangZhengwei MaoFeihe HuangGuocan YuPublished in: Angewandte Chemie (International ed. in English) (2022)
Supramolecular nanomedicines have shown great merits in cancer therapy, but their clinical translation is hampered by monotonous therapeutic modality and unsatisfactory antitumor performance. Herein, a hybrid supramolecular polymeric nanomedicine (SNPs) is developed based on β-cyclodextrin/camptothecin (CPT) host-guest molecular recognition and iron-carboxylate coordination. Iron ions stabilizing SNPs catalyze the conversion of intracellular hydrogen peroxide into highly toxic hydroxyl radical through a Fenton reaction, which further cleaves the thioketal linker of the supramolecular monomer to release potent CPT, thus amplifying the therapeutic efficacy by combining chemodynamic therapy and chemotherapy. The combination therapy stimulates antitumor immunity and promotes intratumoral infiltration of cytotoxic T lymphocytes by triggering immunogenic cell death. In synergy with PD-L1 checkpoint blockade, SNPs enables enhanced immune therapy and a long-term tumor remission.
Keyphrases
- cancer therapy
- hydrogen peroxide
- water soluble
- drug delivery
- combination therapy
- cell death
- genome wide
- energy transfer
- nitric oxide
- dna damage
- genome wide association
- quantum dots
- iron deficiency
- wastewater treatment
- drug release
- rheumatoid arthritis
- locally advanced
- disease activity
- signaling pathway
- single molecule
- ionic liquid
- molecularly imprinted
- mass spectrometry
- systemic lupus erythematosus
- anti inflammatory
- ulcerative colitis