Synchronous Synthesis of Polymeric Vesicles with Controllable Size and Low‐Polydispersity by Polymerization‐Induced Self‐Assembly

Author(s):  
Ren‐Man Zhu ◽  
Cheng‐Lin Yang ◽  
Zi‐Xuan Chang ◽  
Cai‐Yuan Pan ◽  
Wen‐Jian Zhang ◽  
...  
2019 ◽  
Vol 52 (3) ◽  
pp. 1140-1149 ◽  
Author(s):  
Miao Chen ◽  
Jia-Wei Li ◽  
Wen-Jian Zhang ◽  
Chun-Yan Hong ◽  
Cai-Yuan Pan

Pharmaceutics ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1833
Author(s):  
Jingxin Shao ◽  
Shoupeng Cao ◽  
Hanglong Wu ◽  
Loai Abdelmohsen ◽  
Jan van Hest

Bowl-shaped biodegradable polymersomes, or stomatocytes, have much potential as drug delivery systems, due to their intriguing properties, such as controllable size, programmable morphology, and versatile cargo encapsulation capability. In this contribution, we developed well-defined therapeutically active stomatocytes with aggregation-induced emission (AIE) features by self-assembly of biodegradable amphiphilic block copolymers, comprising poly(ethylene glycol) (PEG) and AIEgenic poly(trimethylene carbonate) (PTMC) moieties. The presence of the AIEgens endowed the as-prepared stomatocytes with intrinsic fluorescence, which was employed for imaging of cellular uptake of the particles. It simultaneously enabled the photo-mediated generation of reactive oxygen species (ROS) for photodynamic therapy. The potential of the therapeutic stomatocytes as cargo carriers was demonstrated by loading enzymes (catalase and glucose oxidase) in the nanocavity, followed by a cross-linking reaction to achieve stable encapsulation. This provided the particles with a robust motile function, which further strengthened their therapeutic effect. With these unique features, enzyme-loaded AIEgenic stomatocytes are an attractive platform to be exploited in the field of nanomedicine.


2009 ◽  
Vol 42 (14) ◽  
pp. 5167-5174 ◽  
Author(s):  
Kari Vijayakrishna ◽  
David Mecerreyes ◽  
Yves Gnanou ◽  
Daniel Taton

2015 ◽  
Vol 3 (41) ◽  
pp. 8162-8169 ◽  
Author(s):  
Jing Wei ◽  
Jun Shi ◽  
Qiong Wu ◽  
Liu Yang ◽  
Shaokui Cao

Hollow hydroxyapatite/polyelectrolyte microparticles with controllable size, wall thickness and drug delivery properties have been fabricated via the green hydrothermal method and the LbL self-assembly technique.


RSC Advances ◽  
2021 ◽  
Vol 11 (46) ◽  
pp. 29042-29051
Author(s):  
Fen Zhang ◽  
Yanling Niu ◽  
Yantao Li ◽  
Qian Yao ◽  
Xiaoqi Chen ◽  
...  

Smart polymeric vesicles with both tertiary amine and epoxy functional groups were fabricated for the first time via a reversible addition–fragmentation chain transfer dispersion polymerization approach.


Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2381
Author(s):  
Gina M. DiSalvo ◽  
Abby R. Robinson ◽  
Mohamed S. Aly ◽  
Eric R. Hoglund ◽  
Sean M. O’Malley ◽  
...  

The self-assembly of amphiphilic diblock copolymers into polymeric vesicles, commonly known as polymersomes, results in a versatile system for a variety of applications including drug delivery and microreactors. In this study, we show that the incorporation of hydrophobic plasmonic nanoparticles within the polymersome membrane facilitates light-stimulated release of vesicle encapsulants. This work seeks to achieve tunable, triggered release with non-invasive, spatiotemporal control using single-pulse irradiation. Gold nanoparticles (AuNPs) are incorporated as photosensitizers into the hydrophobic membrane of micron-scale polymersomes and the cargo release profile is controlled by varying the pulse energy and nanoparticle concentration. We have demonstrated the ability to achieve immediate vesicle rupture as well as vesicle poration resulting in temporal cargo diffusion. Additionally, changing the pulse duration, from femtosecond to nanosecond, provides mechanistic insight into the photothermal and photomechanical contributors that govern membrane disruption in this polymer–nanoparticle hybrid system.


2015 ◽  
Vol 137 (4) ◽  
pp. 1412-1415 ◽  
Author(s):  
Juan Li ◽  
Cheng Zheng ◽  
Sena Cansiz ◽  
Cuichen Wu ◽  
Jiehua Xu ◽  
...  

2012 ◽  
Vol 48 (75) ◽  
pp. 9343 ◽  
Author(s):  
Chia-Yen Hsu ◽  
Mu-Ping Nieh ◽  
Ping-Shan Lai

2020 ◽  
Author(s):  
Xiao-Fei Xu ◽  
Ren-Man Zhu ◽  
Cai-Yuan Pan ◽  
Ye-Zi You ◽  
Wen-Jian Zhang ◽  
...  

Abstract The size and shape of polymeric vesicles have great impact on their physicochemical and biological properties. Polymerization-induced self-assembly (PISA) is an efficient method to fabricate vesicles. In most PISA-cases, the formation of vesicles is driven by the solvophobic interactions which are lack of versatility on finely structural regulation. Herein, controlling vesicular size and shape is realized in PISA aided by aromatic interactions. Aromatic interactions between the membrane-forming blocks contribute to the augments of membrane tension which lead to the formation of smaller vesicles (as small as 70 nm), but overly enhanced aromatic interactions result in vesicle fusion rather than size decreasing. When the membrane tension is dominated by aromatic interactions and meanwhile high enough to overcome the energetic barriers of fusion, the aromatic interactions drive vesicle fusion in a directional manner to form tubular structures. The precise regulation of vesicular size and shape in PISA would pave the way to fabricate vesicles for a series of size/shape-dependent applications.


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