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题名

Low-Power Magnetic Resonance-Guided Focused Ultrasound Tumor Ablation upon Controlled Accumulation of Magnetic Nanoparticles by Cascade-Activated DNA Cross-Linkers

作者
通讯作者Wang, Zhongling; Tian, Leilei
发表日期
2022-07-01
DOI
发表期刊
ISSN
1944-8244
EISSN
1944-8252
卷号14期号:28页码:31677-31688
摘要
ABSTRACT: Magnetic resonance-guided focused ultrasound (MRgFUS) is a promising non-invasive surgical technique with spatial specificity and minimal off-target effects. Despite the expanding clinical applications, the major obstacles associated with MRgFUS still lie in low magnetic resonance imaging (MRI) sensitivity and safety issues. High ultrasound power is required to resist the energy attenuation during the delivery to the tumor site and may cause damage to the surrounding healthy tissues. Herein, a surface modification strategy is developed to simultaneously strengthen MRI and ultrasound ablation of MRgFUS by prolonging Fe3O4 nanoparticles' blood circulation and tumorenvironment-triggered accumulation and retention at the tumor site. Specifically, reactive oxygen species-labile methoxy polyethylene glycol and pH-responsive DNA cross-linkers are modified on the surface of Fe3O4 nanoparticles, which can transform nanoparticles into aggregations through the cascade responsive reactions at the tumor site. Notably, DNA is selected as the pH-responsive cross-linker because of its superior biocompatibility as well as the fast and sensitive response to the weak acidity of 6.5-6.8, corresponding to the extracellular pH of tumor tissues. Due to the significantly enhanced delivery and retention amount of Fe3O4 nanoparticles at the tumor site, the MRI sensitivity was enhanced by 1.7-fold. In addition, the ultrasound power was lowered by 35% to reach a sufficient thermal ablation effect. Overall, this investigation demonstrates a feasible resolution to promote the MRgFUS treatment by enhancing the therapeutic efficacy and reducing the side effects, which will be helpful to guide the clinical practice in the future.
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相关链接[来源记录]
收录类别
SCI ; EI
语种
英语
学校署名
第一 ; 通讯
资助项目
National Natural Science Foundation of China["51973089","81971664"] ; Shenzhen Science and Technology Innovation Commission[KQTD20170810111314625] ; Shanghai Pujiang Program[2019PJD044]
WOS研究方向
Science & Technology - Other Topics ; Materials Science
WOS类目
Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary
WOS记录号
WOS:000825425600001
出版者
EI入藏号
20223312579875
EI主题词
Ablation ; Biocompatibility ; Cardiovascular system ; Histology ; Magnetic resonance imaging ; Nanomagnetics ; Nanoparticles ; Resonance ; Tumors ; Ultrasonic applications
EI分类号
Biological Materials and Tissue Engineering:461.2 ; Immunology:461.9.1 ; Heat Transfer:641.2 ; Magnetism: Basic Concepts and Phenomena:701.2 ; Imaging Techniques:746 ; Ultrasonic Applications:753.3 ; Nanotechnology:761 ; Mechanics:931.1 ; Solid State Physics:933
来源库
Web of Science
引用统计
被引频次[WOS]:5
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/356204
专题工学院_材料科学与工程系
作者单位
1.Southern Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China
2.Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Sch Med, Dept Radiol, Shanghai 200080, Peoples R China
第一作者单位材料科学与工程系
通讯作者单位材料科学与工程系
第一作者的第一单位材料科学与工程系
推荐引用方式
GB/T 7714
Zhang, Xindan,Lu, Hongwei,Tang, Na,et al. Low-Power Magnetic Resonance-Guided Focused Ultrasound Tumor Ablation upon Controlled Accumulation of Magnetic Nanoparticles by Cascade-Activated DNA Cross-Linkers[J]. ACS Applied Materials & Interfaces,2022,14(28):31677-31688.
APA
Zhang, Xindan.,Lu, Hongwei.,Tang, Na.,Chen, An.,Wei, Zixiang.,...&Tian, Leilei.(2022).Low-Power Magnetic Resonance-Guided Focused Ultrasound Tumor Ablation upon Controlled Accumulation of Magnetic Nanoparticles by Cascade-Activated DNA Cross-Linkers.ACS Applied Materials & Interfaces,14(28),31677-31688.
MLA
Zhang, Xindan,et al."Low-Power Magnetic Resonance-Guided Focused Ultrasound Tumor Ablation upon Controlled Accumulation of Magnetic Nanoparticles by Cascade-Activated DNA Cross-Linkers".ACS Applied Materials & Interfaces 14.28(2022):31677-31688.
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