Phenylboronic ester-modified anionic micelles for ROS-stimuli response in HeLa cell

Smart polymers as ideal drug nanocarriers have attracted much attention due to the effective drug delivery, internalization and release once triggered by intracellular stimuli, as well as reduced cytotoxicity. We here reported the anionic micelle consisting of copolymer (PEG-b-PAsp) and a PBE (Pheny...

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Main Authors: Qi Y. Wang (Author), Yi S. Xu (Author), Nan X. Zhang (Author), Zhi P. Dong (Author), Bo N. Zhao (Author), Lin C. Liu (Author), Tao Lu (Author), Yue Wang (Author)
Format: Book
Published: Taylor & Francis Group, 2020-01-01T00:00:00Z.
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100 1 0 |a Qi Y. Wang  |e author 
700 1 0 |a Yi S. Xu  |e author 
700 1 0 |a Nan X. Zhang  |e author 
700 1 0 |a Zhi P. Dong  |e author 
700 1 0 |a Bo N. Zhao  |e author 
700 1 0 |a Lin C. Liu  |e author 
700 1 0 |a Tao Lu  |e author 
700 1 0 |a Yue Wang  |e author 
245 0 0 |a Phenylboronic ester-modified anionic micelles for ROS-stimuli response in HeLa cell 
260 |b Taylor & Francis Group,   |c 2020-01-01T00:00:00Z. 
500 |a 1071-7544 
500 |a 1521-0464 
500 |a 10.1080/10717544.2020.1748761 
520 |a Smart polymers as ideal drug nanocarriers have attracted much attention due to the effective drug delivery, internalization and release once triggered by intracellular stimuli, as well as reduced cytotoxicity. We here reported the anionic micelle consisting of copolymer (PEG-b-PAsp) and a PBE (Phenylboronic Ester) group grafted, which can achieve fast response to intracellular ROS and enhanced anti-tumor activity. With this, PEG-b-PAsp-g-PBE/DOX system showed better tumor growth inhibition when studied on HeLa cell lines with high level of intracellular ROS and its subcutaneous tumor models. Additionally, the administration of PEG-b-PAsp-g-PBE/DOX did cause significantly lower systemic toxicity in comparison with free DOX. Hence, PEG-b-PAsp-g-PBE could be a highly efficient and safe nanocarrier to improve the efficacy of chemotherapeutic. 
546 |a EN 
690 |a anionic micelles 
690 |a ros-stimuli response 
690 |a drug delivery system 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Drug Delivery, Vol 27, Iss 1, Pp 681-690 (2020) 
787 0 |n http://dx.doi.org/10.1080/10717544.2020.1748761 
787 0 |n https://doaj.org/toc/1071-7544 
787 0 |n https://doaj.org/toc/1521-0464 
856 4 1 |u https://doaj.org/article/0d883369a3b74512b51b0982ff1bbb83  |z Connect to this object online.