Carrier-Free, Chemophotodynamic Dual Nanodrugs via Self-Assembly for Synergistic Antitumor Therapy

2016 ◽  
Vol 8 (21) ◽  
pp. 13262-13269 ◽  
Author(s):  
Ruiyun Zhang ◽  
Ruirui Xing ◽  
Tifeng Jiao ◽  
Kai Ma ◽  
Chengjun Chen ◽  
...  
Nanoscale ◽  
2017 ◽  
Vol 9 (38) ◽  
pp. 14347-14356 ◽  
Author(s):  
Yan Wen ◽  
Wei Zhang ◽  
Ningqiang Gong ◽  
Yi-Feng Wang ◽  
Hong-Bo Guo ◽  
...  

Carrier-free nanodrug HCPT/Ce6 NRs were prepared through a simple self-assembly approach for chemo-photodynamic combination therapy of tumors in vivo.


2018 ◽  
Vol 15 (6) ◽  
pp. 2466-2478 ◽  
Author(s):  
Lulu Fan ◽  
Bingchen Zhang ◽  
Aixiao Xu ◽  
Zhichun Shen ◽  
Yan Guo ◽  
...  

2017 ◽  
Vol 139 (5) ◽  
pp. 1921-1927 ◽  
Author(s):  
Qianli Zou ◽  
Manzar Abbas ◽  
Luyang Zhao ◽  
Shukun Li ◽  
Guizhi Shen ◽  
...  

Nanoscale ◽  
2019 ◽  
Vol 11 (34) ◽  
pp. 15907-15916 ◽  
Author(s):  
Zhuha Zhou ◽  
Ying Piao ◽  
Lingqiao Hao ◽  
Guanyu Wang ◽  
Zhuxian Zhou ◽  
...  

pH-responsive nanofibers are obtained by the self-assembly of the camptothecin prodrug and surface-coating, which can efficiently enter cancer cells in vitro and penetrate deep into tumor tissue in vivo.


2022 ◽  
Vol 20 (1) ◽  
Author(s):  
Liya Li ◽  
Wangxiao He ◽  
Weiming You ◽  
Jin Yan ◽  
Wenjia Liu

Abstract Background Clinical translation of therapeutic nuclear acid, particularly those targeting tumor progression, has been hampered by the intrinsic weaknesses of nuclear acid therapeutic including poor systemic stability, rapid clearance, low membrane permeability and lack of targeting ability. Small nuclear acid engineered into carrier-free nanodrugs with structural stability and disease targeting may be viable to overcome pharmaceutical obstacles of nuclear acid. Methods A general method through a mild and simple chemistry was established to convert therapeutic miRNA into an infinite Auric-sulfhydryl coordination supramolecular miRNA termed IacsRNA with near-spherical nanostructure, high colloid as well as anti-hydrolysis stability and low macrophage uptakes. Results IacsRNA presented the increased half-life period in circulation and accumulation at tumor sites in comparison to normal miRNA. Moreover, Iacs-miR-30c showed no toxicity of viscera and sanguis system in the 5-time injection dosage of the treatment. More importantly, Iacs-miR-30c potently suppressed the Wnt signaling pathway in vitro and in vivo, and effectively sensitized both potency of 5-Fu in PDX model of colon cancer and Anti-PD1 in B16F10 homograft model of melanoma. Conclusion Collectively, this work amply confirmed the design of IacsRNA as a general and viable strategy of nano-pharmaceutic to concert flimsy therapeutic miRNA into potential drugs. Considering from a broader perspective, the miRNA-initiated infinite coordination self-assembly strategy has distinct advantages in resurrecting nuclear acid therapeutics, probably bringing new inspiration to RNA-derived therapeutics of a great variety of human diseases including cancer. Graphical Abstract


2021 ◽  
Author(s):  
Bo Fan ◽  
Qian Li ◽  
Yanping Jiang ◽  
Weiguang Shen ◽  
Yang Xing ◽  
...  

Abnormal angiogenesis is a hallmark of solid tumors. The combination of cytotoxic and anti-angiogenic drugs has been proved to be more effective than single treatment. As a shining platform, the...


2017 ◽  
Vol 5 (28) ◽  
pp. 5641-5647 ◽  
Author(s):  
Weili Xue ◽  
Liyao Luo ◽  
Yanji Li ◽  
Tian Yin ◽  
Kexin Bian ◽  
...  

Functional gold nanoshells and nanocages were synthesized via self-assembly of lanreotide acetate.


2021 ◽  
Author(s):  
Kaihang Xue ◽  
Feng Wei ◽  
Jinyan Lin ◽  
Haina Tian ◽  
Fukai Zhu ◽  
...  

Novel tumor microenvironment-driven self-targeting supramolecular nanodrugs via ICG-templated small-molecule self-assembly for NIR-II imaging-guided synergistic photothermal–chemotherapy.


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