Dual gatekeepers-modified mesoporous organic silica nanoparticles for synergistic photothermal-chemotherapy of breast cancer

被引:7
|
作者
Wang, Wei [1 ]
Zhong, Fengmin [1 ]
Wang, Dun
Zhao, Yuqi [1 ]
Peng, Dongdong [1 ]
Li, Shuang [1 ]
Ning, Qian [2 ,3 ]
Tang, Shengsong [1 ,2 ,3 ,4 ]
Yu, Cui-Yun [1 ]
Wei, Hua [1 ]
机构
[1] Univ South China, Inst Pharm & Pharmacol, Hunan Prov Cooperat Innovat Ctr Mol Target New Dru, Sch Pharmaceut Sci, Hengyang 421001, Peoples R China
[2] Hunan Univ Med, Sch Pharmaceut Sci, Hunan Prov Key Lab Antibody Based Drug & Intellige, Huaihua 418000, Peoples R China
[3] Hunan Agr Univ, Coll Biosci & Biotechnol, Changsha 410000, Peoples R China
[4] Hunan Prov Key Lab Antibody Based Drug & Intellige, Huaihua 418000, Peoples R China
关键词
Mesoporous organic silica nanoparticles; (MONs); Dual gatekeepers; Drug delivery; Photothermal therapy (PTT); Chemotherapy; DRUG-RELEASE; TUMOR; NANOCAPSULES; BIODEGRADABILITY; DELIVERY;
D O I
10.1016/j.jcis.2023.05.018
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
Hypothesis: Construction of dual gatekeepers-functionalized mesoporous organic silica nanoparticles (MONs) with both physical and chemical mechanisms for modulated drug delivery properties provides one solution to the extracellular stability vs. intracellular high therapeutic efficiency of MONs that hold great potential for clinical translations. Experiments: We reported herein facile construction of diselenium-bridged MONs decorated with dual gatekeepers, i.e., azobenzene (Azo)/polydopamine (PDA) for both physical and chemical modulated drug delivery properties. Specifically, Azo can act as a physical barrier to block DOX in the mesoporous structure of MONs for extracellular safe encapsulation. The PDA outer corona serves not only as a chemical barrier with acidic pHmodulated permeability for double insurance of minimized DOX leakage in the extracellular blood circulation but also for inducing a PTT effect for synergistic PTT and chemotherapy of breast cancer. Findings: An optimized formulation, DOX@(MONs-Azo3)@PDA resulted in approximately 1.5 and 2.4 fold lower IC50 values than DOX@(MONs-Azo3) and (MONs-Azo3)@PDA controls in MCF-7 cells, respectively, and further
引用
收藏
页码:118 / 128
页数:11
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