Aggregation-induced emission polymer nanoparticles with pH-responsive fluorescence

2016 ◽  
Vol 7 (34) ◽  
pp. 5386-5395 ◽  
Author(s):  
Yuming Zhao ◽  
Wen Zhu ◽  
Lixia Ren ◽  
Ke Zhang

A convenient and efficient method was developed to prepare stable polymer nanoparticles with varied morphology and pH-responsive AIE properties, based on the amphiphilic block copolymer self-assembly, crosslinking, and post-functionalization techniques.

Pharmaceutics ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 620 ◽  
Author(s):  
Zhimin Wu ◽  
Manzhen Duan ◽  
Di Xiong ◽  
Can Yang Zhang

It is of great significance to study the structure property and self-assembly of amphiphilic block copolymer in order to effectively and efficiently design and prepare drug delivery systems. In this work, dissipative particle dynamics (DPD) simulation method was used to investigate the structure property and self-assembly ability of pH-responsive amphiphilic block copolymer poly(methyl methacrylate-co-methacrylic acid)-b-poly(aminoethyl methacrylate) (poly(MMA-co-MAA)-b-PAEMA). The effects of different block ratios (hydrophilic PAEMA segment and pH-sensitive PMAA segment) in copolymer on self-assembly and drug loading capacity including drug distribution were extensively investigated. The increase of hydrophilic PAEMA facilitated the formation of a typical core-shell structure as well as a hydrophobic PMAA segment. Furthermore, the optimal drug-carrier ratio was confirmed by an analysis of the drug distribution during the self-assembly process of block copolymer and model drug Ibuprofen (IBU). In addition, the drug distribution and nanostructure of IBU-loaded polymeric micelles (PMs) self-assembled from precise block copolymer (PMMA-b-PMAA-b-PAEMA) and block copolymer (poly(MMA-co-MAA)-b-PAEMA) with random pH-responsive/hydrophobic structure were evaluated, showing that almost all drug molecules were encapsulated into a core for a random copolymer compared to the analogue. The nanostructures of IBU-loaded PMs at different pH values were evaluated. The results displayed that the nanostructure was stable at pH < pKa and anomalous at pH > pKa which indicated drug release, suggesting that the PMs could be used in oral drug delivery. These findings proved that the amphiphilic block copolymer P(MMA30-co-MAA33)-b-PAEMA38 with random structure and pH-sensitivity might be a potential drug carrier. Moreover, DPD simulation shows potential to study the structure property of PMs self-assembled from amphiphilic block copolymer.


2005 ◽  
Vol 42 (3) ◽  
pp. 180-183 ◽  
Author(s):  
S. G. Schulz ◽  
U. Frieske ◽  
H. Kuhn ◽  
G. Schmid ◽  
F. Müller ◽  
...  

2015 ◽  
Vol 6 (10) ◽  
pp. 1817-1829 ◽  
Author(s):  
Lichao Liu ◽  
Leilei Rui ◽  
Yun Gao ◽  
Weian Zhang

The synthesis and self-assembly of ferrocene-containing block copolymers PEG-b-PMAEFc, and the encapsulation and redox-responsive release of a model molecule (rhodamine B) upon external redox stimuli (H2O2).


2019 ◽  
Vol 10 (3) ◽  
pp. 403-411 ◽  
Author(s):  
Mengjiao Cao ◽  
Huijun Nie ◽  
Yuwen Hou ◽  
Guang Han ◽  
Wangqing Zhang

Well-defined multi-arm star thermoresponsive block copolymer nano-assemblies of [poly(N-isopropylacrylamide)-block-polystyrene]n [(PNIPAM-b-PS)n] with n = 1, 2, 3 and 4 arms were synthesized by RAFT dispersion polymerization via polymerization-induced self-assembly.


2016 ◽  
Vol 7 (30) ◽  
pp. 4901-4911 ◽  
Author(s):  
Hua Yuan ◽  
Hai Chi ◽  
Weizhong Yuan

The micelles/aggregates that were self-assembled from a star-shaped copolymer presented redox-responsive behaviour and LCST–UCST thermoresponsive transition.


2017 ◽  
Vol 66 (7) ◽  
pp. 1037-1043 ◽  
Author(s):  
Guoping Li ◽  
Haoxue Dong ◽  
Menghui Liu ◽  
Min Xia ◽  
Chunpeng Chai ◽  
...  

2017 ◽  
Vol 8 (23) ◽  
pp. 3647-3656 ◽  
Author(s):  
Ryoto Tanaka ◽  
Kodai Watanabe ◽  
Takuya Yamamoto ◽  
Kenji Tajima ◽  
Takuya Isono ◽  
...  

The effect of intramolecular cross-linking on aqueous self-assembly behavior was systematically investigated based on an amphiphilic block copolymer system.


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