Fluorescent Silicon Nanorods-Based Nanotheranostic Agents for Multimodal Imaging-Guided Photothermal Therapy
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		    ARTICLE
 
 Cite as Nano-Micro Lett. (2019) 11:73 Received: 6 July 2019 Accepted: 25 August 2019 © The Author(s) 2019
 
 https://doi.org/10.1007/s40820-019-0306-9
 
 Fluorescent Silicon Nanorods‑Based Nanotheranostic Agents for Multimodal Imaging‑Guided Photothermal Therapy Mingyue Cui1, Sangmo Liu1, Bin Song1, Daoxia Guo1, Jinhua Wang1, Guyue Hu1, Yuanyuan Su1 *, Yao He1 * * Yuanyuan Su, [email protected]; Yao He, [email protected] Laboratory of Nanoscale Biochemical Analysis Institute of Functional Nano & Soft Materials (FUNSOM), and Jiangsu Key Laboratory for Carbon‑Based Functional Materials & Devices, Soochow University, 199 Ren’ai Road, Suzhou 215123, Jiangsu, People’s Republic of China
 
 1
 
 HIGHLIGHTS • A kind of multifunctional silicon-based theranostic agent is fabricated and exploited for imaging-guided tumor-targeted photothermal therapy. • The obtained gold nanoparticles-decorated fluorescent silicon nanorods featuring high photothermal conversion performance and good photothermal stability enable a total ablation of tumors and prolong the survival time of mice.
 
 ABSTRACT  The utilization of diagnosis to guide/aid
 
 nanorods (Au@SiNRs), is fabricated and exploited for tumor-targeted multimodal imaging-guided pho‑
 
 Ca2+
 
 O
 
 N
 
 Si
 
 Protein micelle
 
 O
 
 O H N O RGD
 
 NH NH O HN
 
 NH NH
 
 Au@SiNRs AuNPs
 
 RGD-PEG-Au@SiNRs mSH-PEG
 
 Tumor Tissue NIR laser
 
 SiNRs feature high photothermal conversion efficiency mal performance stays constant after five-cycle NIR
 
 OH N HS
 
 2
 
 SiNRs C
 
 HO HN
 
 Step 2
 
 Step 1
 
 PO43−
 
 tothermal therapy. In particular, the prepared Au@ (~ 43.9%) and strong photothermal stability (photother‑
 
 HO
 
 PEG and RGD functionalization Step 3
 
 a kind of multifunctional silicon-based nanostructure, i.e., gold nanoparticles-decorated fluorescent silicon
 
 AuNPs in situ growth
 
 s NP
 
 tion of tumor heterogeneity and complexity. Herein,
 
 Ca2+
 
 PO43−
 
 Crystal growth and aggregation
 
 Au
 
 era of personalized medicine along with the recogni‑
 
 PO43−
 
 Ca2+
 
 O
 
 therapy procedures has shown great prospects in the
 
 Active targeting
 
 laser irradiation), making them high-performance agents for simultaneously photoacoustic and infrared
 
 Tumor neovessels
 
 thermal imaging. The Au@SiNRs are readily modi‑
 
 fied with targeting peptide ligands, enabling an enhanced tumor accumulation with a high value of ~ 8.74% ID g−1. Taking advantages of these unique merits, the Au@SiNRs are superbly suitable for specifically ablating tumors in vivo without appreciable toxicity under the guidance of multimodal imaging. Typically, all the mice treated with the Au@SiNRs remain alive, and no distinct tumor recurrence is observed during 60-day investigation. KEYWORDS  Gold nanoparticle; Fluorescent silicon nanorods; Nanotheranostic; Multimodal imaging; Photothermal therapy; Tumor target
 
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 1 Introduction Along with tremendous advances in cancer nanomedicine, more challenges such as the complexity and heterogeneity of tumors are gradually realized [1, 2]. Using diagnosis to guide/aid therapy procedures w		
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