DNAzyme-assisted bioconstruction of logically activatable nanoplatforms for enhanced cancer therapy

被引:2
|
作者
Wang, Feng [1 ]
Jin, Yi [2 ]
Gao, Xin [1 ]
Huo, Haoran [1 ]
Wang, Bei [2 ]
Niu, Biao [1 ]
Xia, Zihan [2 ]
Zhang, Jinchao [1 ]
Yang, Xinjian [1 ]
机构
[1] Hebei Univ, Inst Life Sci & Green Dev, Coll Chem & Environm Sci, Key Lab Med Chem & Mol Diag,Minist Educ,Chem Biol, Baoding 071002, Peoples R China
[2] Hebei Univ, Coll Basic Med Sci, Key Lab Pathogenesis Mech & Control Inflammatory a, Baoding 071002, Peoples R China
基金
中国国家自然科学基金;
关键词
DNAzyme; Bioconstruction; Gene silencing; Cancer therapy; Activatable nanocarrier; DRUG-RESISTANCE; POLYANILINE; SURVIVIN; ACID; GENE; ACIDIFICATION; RELEASE; ENZYME;
D O I
10.1016/j.jcis.2022.05.080
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
Multifunctional therapeutic nanoplatforms with an activatable property have demonstrated the ability to enhance cancer therapy due to their intrinsic controllability in drug delivery. Although much effort has been focused on constructing multifunctional therapeutic nanoplatforms with an activatable property, developing logically activatable nanoplatforms to exert improved therapeutic efficiency against cancer remains an imperative need. In this study, we established a tumor microenvironment activable nanoplatform by the DNAzyme assisted coating of polyaniline (PANI) on the surface of mesoporous silica nanoparticles (MSNs). This mild synthetic strategy can avoid the destruction of the loaded biomolecules and guarantee the biosafety of the nanoplatforms. Furthermore, the activable polymer can be used to load siRNA for combined cancer treatment. When the composite nanoplatforms were enriched in the tumor, the acidic tumor microenvironment activated the nanocarrier and unloaded the drugs and siRNA upon near-infrared (NIR) irradiation to achieve controlled drug delivery for enhanced cancer therapy. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:1132 / 1141
页数:10
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