Biocompatible PLNP-GNR Composite Nanoplatforms for Monitoring Deep-tissue Photothermal Therapy Process

2021 ◽  
pp. 150189
Author(s):  
Yangqi Meng ◽  
Jian Yang ◽  
Rongyun Jiang ◽  
Shuyue Wang ◽  
Lihua Zheng ◽  
...  
2016 ◽  
Vol 4 (5) ◽  
pp. 782-789 ◽  
Author(s):  
Blanca del Rosal ◽  
Alberto Pérez‐Delgado ◽  
Elisa Carrasco ◽  
Dragana J. Jovanović ◽  
Miroslav D. Dramićanin ◽  
...  

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Xunzhi Wu ◽  
Yongkuan Suo ◽  
Hui Shi ◽  
Ruiqi Liu ◽  
Fengxia Wu ◽  
...  

Abstract Photothermal therapy (PTT) using near-infrared (NIR) light for tumor treatment has triggered extensive attentions because of its advantages of noninvasion and convenience. The current research on PTT usually uses lasers in the first NIR window (NIR-I; 700–900 nm) as irradiation source. However, the second NIR window (NIR-II; 1000–1700 nm) especially NIR-IIa window (1300–1400 nm) is considered much more promising in diagnosis and treatment as its superiority in penetration depth and maximum permissible exposure over NIR-I window. Hereby, we propose the use of laser excitation at 1275 nm, which is approved by Food and Drug Administration for physical therapy, as an attractive technique for PTT to balance of tissue absorption and scattering with water absorption. Specifically, CuS-PEG nanoparticles with similar absorption values at 1275 and 808 nm, a conventional NIR-I window for PTT, were synthesized as PTT agents and a comparison platform, to explore the potential of 1275 and 808 nm lasers for PTT, especially in deep-tissue settings. The results showed that 1275 nm laser was practicable in PTT. It exhibited much more desirable outcomes in cell ablation in vitro and deep-tissue antitumor capabilities in vivo compared to that of 808 nm laser. NIR-IIa laser illumination is superior to NIR-I laser for deep-tissue PTT, and shows high potential to improve the PTT outcome.


2020 ◽  
Author(s):  
Jianou Qiao ◽  
Bo Ye ◽  
Bao Zhao ◽  
Kun Wang ◽  
Yilong Guo ◽  
...  

Abstract Background Neutrophil-based drug delivery system possesses excellent advantages in targeting at tumour because neutrophils are easily recruited by chemotactic factor in tumor microenvironment. Herein, we developed a novel tactic of multistage neutrophils-based nanoparticle delivery system for promoting photothermal therapy (PTT) of lung cancer. Results Au nanorod (AuNR) was successfully modified with bovine serum albumin (AuNRB) and further conjugated with RGD (AuNRBR), followed by neutrophil internalisation to obtain neutrophils-based delivery system (AuNRBR/N). The engineered neutrophils efficiently migrated across the epithelial cells due to inflammatory signal. They exhibited better toxicity against Lewis cells with laser irradiation in vitro. Moreover, AuNRBR/N showed significantly more targetability to tumour tissue compared with cell carrier-free AuNRBR, as demonstrated in Lewis tumour-bearing mice. The enhanced tumour homing efficiency of AuNRBR/N together with subsequently released AuNRBR from the neutrophils was favourable for further deep tissue diffusion and contributed to the inhibition of the tumour growth in PTT and improved survival rate (over 120 days). Conclusions Overall results illustrated that the design of cell-based nanoparticle delivery system for PTT of cancer is promising.


2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Bo Ye ◽  
Bao Zhao ◽  
Kun Wang ◽  
Yilong Guo ◽  
Qinguo Lu ◽  
...  

Abstract Background Neutrophil-based drug delivery system possesses excellent advantages in targeting at tumour because neutrophils are easily recruited by chemotactic factor in tumor microenvironment. Herein, we developed a novel tactic of multistage neutrophils-based nanoparticle delivery system for promoting photothermal therapy (PTT) of lung cancer. Results Au nanorod (AuNR) was successfully modified with bovine serum albumin (AuNRB) and further conjugated with RGD (AuNRBR), followed by neutrophil internalisation to obtain neutrophils-based delivery system (AuNRBR/N). The engineered neutrophils efficiently migrated across the epithelial cells due to inflammatory signal. They exhibited better toxicity against Lewis cells with laser irradiation in vitro. Moreover, AuNRBR/N showed significantly more targetability to tumour tissue compared with cell carrier-free AuNRBR, as demonstrated in Lewis tumour-bearing mice. The enhanced tumour homing efficiency of AuNRBR/N together with subsequently released AuNRBR from the neutrophils was favourable for further deep tissue diffusion and contributed to the inhibition of the tumour growth in PTT and improved survival rate (over 120 days). Conclusions Overall results illustrated that the design of cell-based nanoparticle delivery system for PTT of cancer is promising.


2020 ◽  
Vol 63 (6) ◽  
pp. 1085-1098 ◽  
Author(s):  
Yanxian Guo ◽  
Yang Li ◽  
Wolun Zhang ◽  
Hongru Zu ◽  
Haihong Yu ◽  
...  

2020 ◽  
Author(s):  
Bo Ye ◽  
Bao Zhao ◽  
Kun Wang ◽  
Yilong Guo ◽  
Qinguo Lu ◽  
...  

Abstract Background : Neutrophil-based drug delivery system possesses excellent advantages in targeting at tumour because neutrophils are easily recruited by chemotactic factor in tumor microenvironment. Herein, we developed a novel tactic of multistage neutrophils-based nanoparticle delivery system for promoting photothermal therapy (PTT) of lung cancer. Results: Au nanorod (AuNR) was successfully modified with bovine serum albumin (AuNRB) and further conjugated with RGD (AuNRBR), followed by neutrophil internalisation to obtain neutrophils-based delivery system (AuNRBR/N). The engineered neutrophils efficiently migrated across the epithelial cells due to inflammatory signal. They exhibited better toxicity against Lewis cells with laser irradiation in vitro . Moreover, AuNRBR/N showed significantly more targetability to tumour tissue compared with cell carrier-free AuNRBR, as demonstrated in Lewis tumour-bearing mice. The enhanced tumour homing efficiency of AuNRBR/N together with subsequently released AuNRBR from the neutrophils was favourable for further deep tissue diffusion and contributed to the inhibition of the tumour growth in PTT and improved survival rate (over 120 days). Conclusions: Overall results illustrated that the design of cell-based nanoparticle delivery system for PTT of cancer is promising.


2021 ◽  
Author(s):  
Mingming Xing ◽  
Lihua Kang ◽  
Xingyu Wu ◽  
Pang Tao ◽  
Hong Wang ◽  
...  

Red upconversion luminescent (UCL) nanoparticles are of significant importance for applications in the fields of deep tissue imaging, photothermal therapy and security ink. In this work, high-efficient red emission was...


Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 773
Author(s):  
Yunying Zhao ◽  
Zheng He ◽  
Qiang Zhang ◽  
Jing Wang ◽  
Wenying Jia ◽  
...  

Photothermal therapy (PTT) has received constant attention as an efficient cancer therapy method due to locally selective treatment, which is not affected by the tumor microenvironment. In this study, a novel 880 nm near-infrared (NIR) laser-triggered photothermal agent (PTA), 3TT-IC-4Cl, was used for PTT of a tumor in deep tissue. Folic acid (FA) conjugated amphiphilic block copolymer (folic acid-polyethylene glycol-poly (β-benzyl-L-aspartate)10, FA-PEG-PBLA10) was employed to encapsulate 3TT-IC-4Cl by nano-precipitation to form stable nanoparticles (TNPs), and TNPs exhibit excellent photothermal stability and photothermal conversion efficiency. Furthermore, the in vitro results showed TNPs display excellent biocompatibility and significant phototoxicity. These results suggest that 880 nm triggered TNPs have great potential as effective PTAs for photothermal therapy of tumors in deep tissue.


2021 ◽  
Author(s):  
Shubi Zhao ◽  
Yiqun Luo ◽  
Zong Chang ◽  
Chenchen Liu ◽  
Tong Li ◽  
...  

Abstract The second near infrared window is considered to be the optimal optical window for medical imaging and therapy as the deep tissue penetration. A series gold nanorods with large aspect ratio have been synthesized. Strong plasma absorption in the second near infrared window from 1000 nm to 1300 nm could be observed. The biocompatibility of the synthesized gold nanorods is dramatically improved via coating by bovine serum albumin (BSA), while the optical properties of which remains. The breast cancer tumor-bearing mouse could be well treated by the prepared gold nanorods with the NIR-II light intensity as low as 0.75 W/cm2. In summary, these results prove the feasibility of using low dose to treat tumor in the NIR-II region.


Nanomedicine ◽  
2021 ◽  
Author(s):  
Yu-Qi Liu ◽  
Li-Ying Qin ◽  
Hong-Jiao Li ◽  
Yi-Xi Wang ◽  
Rui Zhang ◽  
...  

With the excellent ability to transform near-infrared light to localized visible or UV light, thereby achieving deep tissue penetration, lanthanide ion-doped upconversion nanoparticles (UCNP) have emerged as one of the most striking nanoscale materials for more effective and safer cancer treatment. Up to now, UCNPs combined with photosensitive components have been widely used in the delivery of chemotherapy drugs, photodynamic therapy and photothermal therapy. Applications in these directions are reviewed in this article. We also highlight microenvironmental tumor monitoring and precise targeted therapies. Then we briefly summarize some new trends and the existing challenges for UCNPs. We hope this review can provide new ideas for future cancer treatment based on UCNPs.


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