Self-assembled, dual drug carrying polymer-drug conjugate for co-delivery

2015 ◽  
Vol 213 ◽  
pp. e139-e140 ◽  
Author(s):  
Yan Li ◽  
Donglu Shi ◽  
Yongyong Li
2015 ◽  
Vol 12 (6) ◽  
pp. 782-794 ◽  
Author(s):  
Megha Matlapudi ◽  
Afrasim Moin ◽  
Raghavender Medishetti ◽  
K. Rajendra ◽  
Ashok Raichur ◽  
...  
Keyword(s):  

2019 ◽  
Vol 101 ◽  
pp. 448-463 ◽  
Author(s):  
Piyush Kumar Gupta ◽  
Sreenath Pappuru ◽  
Santosh Gupta ◽  
Bamadeb Patra ◽  
Debashis Chakraborty ◽  
...  

2018 ◽  
Vol 548 (1) ◽  
pp. 357-374 ◽  
Author(s):  
Varun Kushwah ◽  
Sameer S. Katiyar ◽  
Ashish Kumar Agrawal ◽  
Isha Saraf ◽  
Inder Pal Singh ◽  
...  

2007 ◽  
Vol 4 (5) ◽  
pp. 659-667 ◽  
Author(s):  
Christopher P. Leamon ◽  
Joseph A. Reddy ◽  
Iontcho R. Vlahov ◽  
Elaine Westrick ◽  
Alicia Dawson ◽  
...  

2018 ◽  
Vol 6 (7) ◽  
pp. 1818-1833 ◽  
Author(s):  
Yang Li ◽  
Huabing Zhang ◽  
Yilin Chen ◽  
Jinyuan Ma ◽  
Jinyan Lin ◽  
...  

A novel synergistic-targeting polymeric delivery system was developed to carry drug–drug conjugate for boosting dual-drug co-delivery and combinational tumor therapy.


RSC Advances ◽  
2016 ◽  
Vol 6 (4) ◽  
pp. 2602-2610 ◽  
Author(s):  
Yanna Zhao ◽  
Jing Zhao ◽  
Chunying Hao ◽  
Meihua Han ◽  
Mincan Wang ◽  
...  

An amphiphilic dendron–drug conjugate was synthesized via oligoethylene glycol (OEG) dendrons coupled with anticancer drug doxorubicin (DOX).


2018 ◽  
Vol 10 (34) ◽  
pp. 28301-28313 ◽  
Author(s):  
Gang-Gang Yang ◽  
Liang Hao ◽  
Qian Cao ◽  
Hang Zhang ◽  
Jing Yang ◽  
...  

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Xuelin Xia ◽  
Xiaoyuan Yang ◽  
Wei Huang ◽  
Xiaoxia Xia ◽  
Deyue Yan

AbstractAffibody molecules are small non-immunoglobulin affinity proteins, which can precisely target to some cancer cells with specific overexpressed molecular signatures. However, the relatively short in vivo half-life of them seriously limited their application in drug targeted delivery for cancer therapy. Here an amphiphilic affibody-drug conjugate is self-assembled into nanomicelles to prolong circulation time for targeted cancer therapy. As an example of the concept, the nanoagent was prepared through molecular self-assembly of the amphiphilic conjugate of ZHER2:342-Cys with auristatin E derivate, where the affibody used is capable of binding to the human epidermal growth factor receptor 2 (HER2). Such a nanodrug not only increased the blood circulation time, but also enhanced the tumor targeting capacity (abundant affibody arms on the nanoagent surface) and the drug accumulation in tumor. As a result, this affibody-based nanoagent showed excellent antitumor activity in vivo to HER2-positive ovary and breast tumor models, which nearly eradicated both small solid tumors (about 100 mm3) and large established tumors (exceed 500  mm3). The relative tumor proliferation inhibition ratio reaches 99.8% for both models.


Sign in / Sign up

Export Citation Format

Share Document