scholarly journals Hydrophilic mesoporous carbon nanospheres with high drug-loading efficiency for doxorubicin delivery and cancer therapy

2016 ◽  
pp. 1793 ◽  
Author(s):  
Feng Yang ◽  
Huan Wang ◽  
Xiangui Li ◽  
Zhiqiang Ma ◽  
Dan Wang ◽  
...  
Nanoscale ◽  
2019 ◽  
Vol 11 (35) ◽  
pp. 16351-16361 ◽  
Author(s):  
Yuwei Qiu ◽  
Dandan Ding ◽  
Wenjing Sun ◽  
Yushuo Feng ◽  
Doudou Huang ◽  
...  

Hollow mesoporous carbon nanospheres were able to achieve high drug loading, excellent photoacoustic imaging ability and photothermal conversion efficacy, enabling imaging-guided light-activated synergistic therapy.


2017 ◽  
Vol 156 ◽  
pp. 29-37 ◽  
Author(s):  
Yongpeng Hou ◽  
Chen Yao ◽  
Longbing Ling ◽  
Yawei Du ◽  
Ruiyu He ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (91) ◽  
pp. 88248-88254 ◽  
Author(s):  
Dandan Xu ◽  
Rui Xie ◽  
Tongying Xu ◽  
Xuejie Guo ◽  
Qi Liu ◽  
...  

Fe3O4@CS nanoparticles as the precursors were encapsulated by PA, developing Fe3O4@CS@PA nanocarriers with high drug loading efficiency, outstanding magnetic saturation, remarkable pH-response and obvious inhibition to tumor cells.


2020 ◽  
Vol 8 (3) ◽  
pp. 949-959 ◽  
Author(s):  
Yuchen Wu ◽  
Shixian Lv ◽  
Yongjuan Li ◽  
Hua He ◽  
Yong Ji ◽  
...  

The introduction of donor-receptor coordination between micelles and drug payloads provides a precise co-delivery strategy for two different chemo-drugs with high drug loading and ROS responsiveness.


2019 ◽  
Vol 7 (37) ◽  
pp. 5677-5687 ◽  
Author(s):  
Li Zhang ◽  
Dongjian Shi ◽  
Chunling Shi ◽  
Tatsuo Kaneko ◽  
Mingqing Chen

A novel multi-arm polyphosphoester-based nanomaterial provides high drug loading efficiency and sustained-release drug delivery for effective chemotherapy.


2013 ◽  
Vol 42 (24) ◽  
pp. 8918 ◽  
Author(s):  
Baixiang Wang ◽  
Weiyan Meng ◽  
Ming Bi ◽  
Yuxin Ni ◽  
Qing Cai ◽  
...  

2018 ◽  
Vol 166 ◽  
pp. 235-244 ◽  
Author(s):  
Shuo Fang ◽  
Yongpeng Hou ◽  
Longbing Ling ◽  
Danquan Wang ◽  
Muhammad Ismail ◽  
...  

2020 ◽  
Vol 6 (45) ◽  
pp. eabc1725
Author(s):  
Yinxian Yang ◽  
Bingjun Sun ◽  
Shiyi Zuo ◽  
Ximu Li ◽  
Shuang Zhou ◽  
...  

Rational design of nanoparticulate drug delivery systems (nano-DDS) for efficient cancer therapy is still a challenge, restricted by poor drug loading, poor stability, and poor tumor selectivity. Here, we report that simple insertion of a trisulfide bond can turn doxorubicin homodimeric prodrugs into self-assembled nanoparticles with three benefits: high drug loading (67.24%, w/w), high self-assembly stability, and high tumor selectivity. Compared with disulfide and thioether bonds, the trisulfide bond effectively promotes the self-assembly ability of doxorubicin homodimeric prodrugs, thereby improving the colloidal stability and in vivo fate of prodrug nanoassemblies. The trisulfide bond also shows higher glutathione sensitivity compared to the conventional disulfide bond, and this sensitivity enables efficient tumor-specific drug release. Therefore, trisulfide bond–bridged prodrug nanoassemblies exhibit high selective cytotoxicity on tumor cells compared with normal cells, notably reducing the systemic toxicity of doxorubicin. Our findings provide new insights into the design of advanced redox-sensitive nano-DDS for cancer therapy.


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