Se-modified gold nanorods for enhancing the photothermal therapy efficiency--avoiding the off-target problem induced by biothiols

Author(s):  
Bo Hu ◽  
Zengteng Zhao ◽  
Xiaonan Gao ◽  
Xiaoxiao Song ◽  
Zihao Xu ◽  
...  

Tumor-targeted gold nanorods (AuNRs) assembled through Au-S bond have been widely used for photothermal therapy (PTT) via intravenous injection. However, with long time in vivo circulation, biothiols can replace some...

2017 ◽  
Vol 114 (15) ◽  
pp. E3110-E3118 ◽  
Author(s):  
Moustafa R. K. Ali ◽  
Mohammad Aminur Rahman ◽  
Yue Wu ◽  
Tiegang Han ◽  
Xianghong Peng ◽  
...  

Gold nanorods (AuNRs)-assisted plasmonic photothermal therapy (AuNRs-PPTT) is a promising strategy for combating cancer in which AuNRs absorb near-infrared light and convert it into heat, causing cell death mainly by apoptosis and/or necrosis. Developing a valid PPTT that induces cancer cell apoptosis and avoids necrosis in vivo and exploring its molecular mechanism of action is of great importance. Furthermore, assessment of the long-term fate of the AuNRs after treatment is critical for clinical use. We first optimized the size, surface modification [rifampicin (RF) conjugation], and concentration (2.5 nM) of AuNRs and the PPTT laser power (2 W/cm2) to achieve maximal induction of apoptosis. Second, we studied the potential mechanism of action of AuNRs-PPTT using quantitative proteomic analysis in mouse tumor tissues. Several death pathways were identified, mainly involving apoptosis and cell death by releasing neutrophil extracellular traps (NETs) (NETosis), which were more obvious upon PPTT using RF-conjugated AuNRs (AuNRs@RF) than with polyethylene glycol thiol-conjugated AuNRs. Cytochrome c and p53-related apoptosis mechanisms were identified as contributing to the enhanced effect of PPTT with AuNRs@RF. Furthermore, Pin1 and IL18-related signaling contributed to the observed perturbation of the NETosis pathway by PPTT with AuNRs@RF. Third, we report a 15-month toxicity study that showed no long-term toxicity of AuNRs in vivo. Together, these data demonstrate that our AuNRs-PPTT platform is effective and safe for cancer therapy in mouse models. These findings provide a strong framework for the translation of PPTT to the clinic.


Author(s):  
Seungsoo Kim ◽  
Yun-Sheng Chen ◽  
Geoffrey P. Luke ◽  
Mohammad Mehrmohammadi ◽  
Jason R. Cook ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (20) ◽  
pp. 5235
Author(s):  
Galina M. Proshkina ◽  
Elena I. Shramova ◽  
Marya V. Shilova ◽  
Ivan V. Zelepukin ◽  
Victoria O. Shipunova ◽  
...  

Near-infrared phototherapy has great therapeutic potential for cancer treatment. However, for efficient application, in vivo photothermal agents should demonstrate excellent stability in blood and targeted delivery to pathological tissue. Here, we demonstrated that stable bovine serum albumin-coated gold mini nanorods conjugated to a HER2-specific designed ankyrin repeat protein, DARPin_9-29, selectively accumulate in HER2-positive xenograft tumors in mice and lead to a strong reduction in the tumor size when being illuminated with near-infrared light. The results pave the way for the development of novel DARPin-based targeted photothermal therapy of cancer.


2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
Oshra Betzer ◽  
Rinat Ankri ◽  
Menachem Motiei ◽  
Rachela Popovtzer

A critical problem in the treatment of cancer is the inability to identify microsized tumors and treat them without normal tissue destruction. While surgical excision of tumors is highly effective, residual micrometastases and remaining positive margins are the main cause of recurrence. In this study, we propose a theranostic approach for the detection and therapy of head and neck cancer (HNC). We developed a plasmonic-based nanoplatform for combined, ultrasensitivein vivospectroscopic detection and targeted therapy of HNC. This detection method involves near-infrared (NIR) spectroscopy of gold nanorods (GNRs) that selectively target and attach to squamous cell carcinoma HNC cells, through an immune complex. Diagnosis is based on a spectral shift analysis, which is generated by interparticle-plasmon-resonance patterns of the specifically targeted GNRs. Additionally, the ability to design the GNRs to strongly absorb light in the NIR region enables efficient irradiation of these GNRs, for selective photothermal therapy (PTT) of the cancer cells. We expect this targeted, noninvasive, and nonionizing spectroscopic detection method to provide a highly sensitive and simple diagnostic tool for micrometastasis. In addition, the concomitant development of targeted PTT, based on specific cancer markers, may pave the way for tailoring effective therapy for patients, toward an era of personalized medicine.


2012 ◽  
Vol 24 (03) ◽  
pp. 229-235 ◽  
Author(s):  
Shuhua Zhao ◽  
Xinli Lin ◽  
Long Zhang ◽  
Lei Sun ◽  
Jun Li ◽  
...  

To observe acute toxicity of naked Fe3O4 -nanoparticles in mice, ICR mice were selected and exposed once to naked Fe3O4 -nanoparticles by tail intravenous injection with different doses, i.e. 0, 102.4, 128, 160, 200, 250 mg/kg of body weight. 15 days later, Fe3O4 distribution and pathologic changes in main organs were investigated. By tail intravenous injection, LD50 of naked Fe3O4 -nanoparticles in mice was 163.60 mg/kg of body weight (147.58, 181.37 mg/kg of body weight, 95% confidence interval). Deaths of mice mainly caused by decompensation and twitching were observed. Immediately after injection, nanoparticles performed fast distribution in lung, liver, spleen etc, yet little were traced in brain, heart and kidney. 15 days after injection, apparent decline of nanoparticles content in lung and spleen was observed, whereas in liver the content rose. Pathologic detection indicated local particle denaturation and necrosis in the cardiac tissue. Protein cast was seen in several kidney tubules, and extravasated blood in carunculae papillaris, yet no pathologic changes were observed in other organs. LD50 of Fe3O4 nanoparticles (9 nm) by means of tail intravenous injection is 163.60 mg/kg, and they mainly distributed in liver, spleen, lung and caused denaturation and necrosis in the cardiac muscle and malfunction of kidney. Also, the process of excreting the particles takes a long time.


Nanomedicine ◽  
2015 ◽  
Vol 10 (11) ◽  
pp. 1723-1733 ◽  
Author(s):  
Robert CG Martin ◽  
Erica Locatelli ◽  
Yan Li ◽  
Weizhong Zhang ◽  
Suping Li ◽  
...  

Nanoscale ◽  
2015 ◽  
Vol 7 (33) ◽  
pp. 13991-14001 ◽  
Author(s):  
Jinbao Qin ◽  
Zhiyou Peng ◽  
Bo Li ◽  
Kaichuang Ye ◽  
Yuxin Zhang ◽  
...  

This study shows that Au nanorods are a promising theranostic platform for the diagnosis and photothermal therapy of inflammation associated diseases.


2009 ◽  
Vol 7 (1) ◽  
pp. 94-104 ◽  
Author(s):  
Zhiming Li ◽  
Peng Huang ◽  
Xuejun Zhang ◽  
Jing Lin ◽  
Sen Yang ◽  
...  

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