Reactive oxygen species-responsive clicked assembly of gold nanoparticles to enhance photothermal therapy

被引:10
|
作者
Bui, Hoai-Thuong Duc [1 ]
Park, Yeonju [2 ]
Jung, Young Mee [2 ,3 ,4 ]
Chew, Sing Yian [5 ,6 ,7 ]
Yoo, Hyuk Sang [1 ,2 ]
机构
[1] Kangwon Natl Univ, Dept Med Biomat Engn, Chunchon 24341, South Korea
[2] Kangwon Natl Univ, Kangwon Radiat Convergence Res Support Ctr, Chunchon 24341, South Korea
[3] Kangwon Natl Univ, Inst Mol Sci & Fus Technol, Dept Chem, Chunchon 24341, South Korea
[4] Kangwon Natl Univ, Kangwon Inst Inclus Technol, Chunchon 24341, South Korea
[5] Nanyang Technol Univ, Sch Chem Chem Engn & Biotechnol, Singapore 637459, Singapore
[6] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 308232, Singapore
[7] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
关键词
COPPER; CHEMISTRY; SIZE; ROS;
D O I
10.1039/d3tb00500c
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
To enhance the efficacy of photothermal therapy (PTT) at tumor sites, we designed a reactive oxygen species (ROS)-responsive gold nanoparticle (AuNP)-based nanosystem in which azide-decorated AuNPs (N-3@AuNPs) and diselenide-coated alkyne-decorated AuNPs (Se/Ak@AuNPs) were separately prepared for selective clicking into nanoclusters when exposed to ROS. Se/Ak@AuNPs were dual-functionalized with alkyne moieties and diselenide linkers embedded in a long chain of polyethylene glycol (PEG) to enable the alkyne moieties of Se/Ak@AuNPs to be inaccessible to the azide moieties of N-3@AuNPs owing to steric hindrance. At tumor sites where the ROS level is elevated due to the increased metabolic activity, cellular receptor signaling, mitochondrial dysfunction, and oncogene activity, the diselenide linkers were cleaved, leading to the liberation of the long PEG chains tethered to AuNPs, and the alkyne moieties could be recognized by the surrounding azide moieties to generate a click reaction. The clicked AuNPs formed clustered nanoparticles with increased size. Upon 808 nm laser irradiation, these large clusters of AuNPs significantly enhanced the photothermal conversion efficiency compared with that of isolated AuNPs. In vitro studies revealed that the AuNP clusters exhibited a noticeably higher apoptosis rate than AuNPs. Therefore, ROS-responsive clicked AuNP clusters can be a potential tool for PTT enhancement in cancer treatment.
引用
收藏
页码:6961 / 6974
页数:14
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