MnO2-shelled Doxorubicin/Curcumin nanoformulation for enhanced colorectal cancer chemo-immunotherapy

被引:26
|
作者
Liu, Jie [1 ]
Li, Li [1 ]
Zhang, Bing [2 ]
Xu, Zhi Ping [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[2] Queensland Govt Dept Agr & Fisheries, St Lucia, Qld, Australia
基金
澳大利亚研究理事会;
关键词
Immunostimulatory nanomedicine; Curcumin; Doxorubicin; MnO2; Colorectal cancer combination treatment; TUMOR MICROENVIRONMENT; BREAST-CANCER; CURCUMIN; MANGANESE; EFFICACY; THERAPY; SHAPE; CHEMISTRY; RESPONSES; CYSTEINE;
D O I
10.1016/j.jcis.2022.02.132
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Metallodrug platinum compounds are indispensable components in the current standard combination for colorectal cancer treatment yet with severe additional adverse effects compromising the clinical out-comes. Having tumor microenvironment modulation and immunostimulatory effect, bio-compatible manganese (Mn) materials hold great promise for developing alternate metallodrug combination treat-ments. In this research, a novel MnO2-shelled nanoplatform was constructed to load two FDA-approved anti-tumor drugs, i.e., immunomodulatory curcumin (Cur) and immunostimulatory doxoru-bicin (Dox) to achieve enhanced dual-chemotherapy of primary tumors and remarkable inhibition of dis -tant colorectal tumors. The experimental results have shown that MnO2 efficiently enhanced Dox/Cur chemotherapy with significant primary tumor inhibition (81%) at very low dosages (5.0 and 1.0 mg/kg of Cur and Dox, respectively). Furthermore, the MnO2-assisted Dox/Cur chemotherapy promoted strong tumoricidal adaptive immune responses and overwhelmingly inhibited tumorigenesis in the tumor rechallenge experiment. This work has thus demonstrated the promising efficacy of the Mn/Dox/Cur nano-formulation and provided a novel way to improve immunostimulation of conventional chemother-apeutics using active metal oxide nanomaterials for colorectal cancer treatment. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:315 / 325
页数:11
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