Magneto-plasmonic nanostars for image-guided and NIR-triggered drug delivery

被引:62
作者
Tomitaka, Asahi [1 ]
Arami, Hamed [2 ,3 ]
Ahmadivand, Arash [4 ]
Pala, Nezih [5 ]
McGoron, Anthony J. [6 ]
Takemura, Yasushi [7 ]
Febo, Marcelo [8 ]
Nair, Madhavan [1 ]
机构
[1] Florida Int Univ, Ctr Personalized Nanomed,Herbert Wertheim Coll Me, Dept Immunol & Nanomed, Inst NeuroImmune Pharmacol, Miami, FL 33199 USA
[2] Stanford Univ, James H Clark Ctr, Mol Imaging Program Stanford MIPS, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
[4] Rice Univ, Dept Elect & Comp Engn, Houston, TX 77005 USA
[5] Florida Int Univ, Dept Elect & Comp Engn, Miami, FL 33174 USA
[6] Florida Int Univ, Dept Biomed Engn, Miami, FL 33174 USA
[7] Yokohama Natl Univ, Dept Elect & Comp Engn, Yokohama, Kanagawa 2408501, Japan
[8] Univ Florida, Coll Med, Dept Psychiat, McKnight Brain Inst, Gainesville, FL 32611 USA
基金
美国国家科学基金会;
关键词
IRON-OXIDE NANOPARTICLES; GOLD NANOPARTICLES; CONTRAST AGENTS; MRI; RESONANCES; THERAPY; CELLS; CORE;
D O I
10.1038/s41598-020-66706-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Smart multifunctional nanoparticles with magnetic and plasmonic properties assembled on a single nanoplatform are promising for various biomedical applications. Owing to their expanding imaging and therapeutic capabilities in response to external stimuli, they have been explored for on-demand drug delivery, image-guided drug delivery, and simultaneous diagnostic and therapeutic (i.e. theranostic) applications. In this study, we engineered nanoparticles with unique morphology consisting of a superparamagnetic iron oxide core and star-shaped plasmonic shell with high-aspect-ratio gold branches. Strong magnetic and near-infrared (NIR)-responsive plasmonic properties of the engineered nanostars enabled multimodal quantitative imaging combining advantageous functions of magnetic resonance imaging (MRI), magnetic particle imaging (MPI), photoacoustic imaging (PAI), and image-guided drug delivery with a tunable drug release capacity. The model drug molecules bound to the core-shell nanostars were released upon NIR illumination due to the heat generation from the core-shell nanostars. Moreover, our simulation analysis showed that the specific design of the core-shell nanostars demonstrated a pronounced multipolar plasmon resonance, which has not been observed in previous reports. The multimodal imaging and NIR-triggered drug release capabilities of the proposed nanoplatform verify their potential for precise and controllable drug release with different applications in personalized medicine.
引用
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页数:10
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