Enzyme catalysis-induced RAFT polymerization in water for the preparation of epoxy-functionalized triblock copolymer vesicles

2018 ◽  
Vol 9 (39) ◽  
pp. 4908-4916 ◽  
Author(s):  
Qin Xu ◽  
Yuxuan Zhang ◽  
Xueliang Li ◽  
Jun He ◽  
Jianbo Tan ◽  
...  
Keyword(s):  
Enzyme Catalysis ◽  
Triblock Copolymer ◽  
Room Temperature ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Reversible Addition

Enzyme catalysis-induced aqueous reversible addition–fragmentation chain transfer (RAFT) polymerization was conducted at room temperature for the preparation of epoxy-functionalized triblock copolymer vesicles.

Synthesis of Zwitterionic Chimeric Polymersomes for Efficient Protein Loading and Intracellular Delivery

2021 ◽  
Author(s):  
bingbing zhao ◽  
Yuting Yan ◽  
Junmei Zhang ◽  
Enping Chen ◽  
Ke Wang ◽  
...  
Keyword(s):  
Ring Opening ◽  
Triblock Copolymer ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Intracellular Delivery ◽  
Ring Opening Polymerization ◽  
H Nmr ◽  
Protein Loading ◽  
Reversible Addition

A novel zwitterionic triblock copolymer of poly(dimethylamino carbonate)-polycaprolactone-poly((2-(methacryloyloxy)ethyl)dimethyl-(3-sulfopropyl)ammonium) [PAC(DMA)-PCL-PMDMSA] was designed and synthesized via sequential ring-opening polymerization (ROP) and reversible addition-fragmentation chain transfer (RAFT) polymerization successively. The 1H NMR and...

Room temperature synthesis of block copolymer nano-objects with different morphologies via ultrasound initiated RAFT polymerization-induced self-assembly (sono-RAFT-PISA)

2020 ◽  
Vol 11 (21) ◽  
pp. 3564-3572
Author(s):  
Jing Wan ◽  
Bo Fan ◽  
Yiyi Liu ◽  
Tina Hsia ◽  
Kaiyuan Qin ◽  
...  
Keyword(s):  
Block Copolymer ◽  
Self Assembly ◽  
Room Temperature ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Aqueous System ◽  
Temperature Synthesis ◽  
Room Temperature Synthesis ◽  
System P ◽  
Reversible Addition

The first room temperature synthesis of diblock copolymer nano-objects with different morphologies using ultrasound (990 kHz) initiated reversible addition-fragmentation chain transfer PISA (sono-RAFT-PISA) in aqueous system.

Synthesis, self-assembly and self-healing properties of organic–inorganic ABA triblock copolymers with poly(POSS acrylate) endblocks

2019 ◽  
Vol 10 (19) ◽  
pp. 2424-2435 ◽  
Author(s):  
Bingjie Zhao ◽  
Sen Xu ◽  
Sixun Zheng
Keyword(s):  
Self Assembly ◽  
Triblock Copolymer ◽  
Chain Transfer ◽  
Triblock Copolymers ◽  
Raft Polymerization ◽  
Self Healing ◽  
Reversible Addition ◽  
Aba Triblock Copolymer

A novel organic–inorganic ABA triblock copolymer with a poly(acrylate amide) (PAA) midblock and poly(POSS acrylate) [P(POSS)] endblocks was synthesized via sequential reversible addition–fragmentation chain transfer (RAFT) polymerization.

UV light-initiated RAFT polymerization induced self-assembly

2015 ◽  
Vol 6 (34) ◽  
pp. 6129-6132 ◽  
Author(s):  
Zhenzhong Liu ◽  
Gongjun Zhang ◽  
Wei Lu ◽  
Youju Huang ◽  
Jiawei Zhang ◽  
...  
Keyword(s):  
Self Assembly ◽  
Room Temperature ◽  
Chain Transfer ◽  
Uv Light ◽  
Raft Polymerization ◽  
Reversible Addition ◽  
New Strategy

Reversible addition–fragmentation chain transfer (RAFT) polymerization induced self-assembly (PISA) initiated by UV light is exploited as a new strategy to prepare polymeric nanomicelles at room temperature.

scholarly journals Comparison of Thermoresponsive Hydrogels Synthesized by Conventional Free Radical and RAFT Polymerization

Materials ◽  
2019 ◽  
Vol 12 (17) ◽  
pp. 2697 ◽  
Author(s):  
Fanny Joubert ◽  
Peyton Cheong Phey Denn ◽  
Yujie Guo ◽  
George Pasparakis
Keyword(s):  
Free Radical ◽  
Room Temperature ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Hydrolytic Stability ◽  
Monomer Concentration ◽  
Crosslinking Density ◽  
Dye Release ◽  
Reversible Addition ◽  
Thermoresponsive Hydrogels

We compared the influence of the polymerization mechanism onto the physical characteristics of thermoresponsive hydrogels. The Poly(N-isopropylacrylamide) (PNIPAAm) hydrogels were successfully synthesized using reversible addition-fragmentation chain-transfer (RAFT) and free radical polymerization (FRP). The gels were prepared while using different crosslinker feed and monomer concentration. The swelling, dye release, and hydrolytic stability of the gels were investigated in water, or in representative komostrope and chaotrope salt solutions at room temperature and at 37 °C. It was found that the swelling ratio (SR) of the RAFT gels was significantly higher than that of the FRP gels; however, an increased crosslinking density resulted in a decrease of the SR of the RAFT gels as compared to the corresponding gels that are made by FRP, which indicates the limitation of the cross-linking efficiency that is attained in RAFT polymerization. Additionally, an increased monomer concentration decreased the SR of the RAFT gels, whereas a similar SR was observed for the FRP gels. However, the SR of both RAFT and FRP gels in NaSCN and Na2SO4 solutions were similar. Finally, the rate of dye release was significantly slower from the RAFT gels than the FRP gels and the hydrolytic stability of the RAFT gels was lower than that of FRP gels in water, but maintained similar stability in Na2SO4 and NaSCN solutions.

Preparation of Thermo-Sensitive Supramolecular Hydrogels Formed from MPEG-b-PNIPAM-b-MPEG Triblock Copolymer with α-Cyclodextrin

2014 ◽  
Vol 934 ◽  
pp. 75-79 ◽  
Author(s):  
Xiao Feng Ye ◽  
Mi Zhou ◽  
Jing Ying Hu ◽  
Xin Qian
Keyword(s):  
Triblock Copolymer ◽  
Chain Transfer ◽  
Triblock Copolymers ◽  
Raft Polymerization ◽  
Inclusion Complexation ◽  
Gel Permeation Chromatography ◽  
H Nmr ◽  
Reversible Addition ◽  
Response Interval ◽  
Gel Permeation

To develop a new drug delivery matrix with the suitable responsive interval, a well-defined triblock copolymer MPEG-b-PNIPAM-b-MPEG was synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization. Then, the supramolecular hydrogels were fabricated via inclusion complexation with α-cyclodextrin (α-CD) and the triblock copolymers in aqueous solutions. The triblock copolymers were characterized by 1H NMR and gel permeation chromatography (GPC), and the supramolecular structures of hydrogels was confirmed by DSC. The resultant hydrogels was found to be thermo-sensitive, and the response interval could be modulated by controlling the content of PNIPAM.

Diverse nanostructures and gel behaviours contained in a thermo- and dual-pH-sensitive ABC (PNIPAM–PAA–P4VP) terpolymer in an aqueous solution

RSC Advances ◽  
2016 ◽  
Vol 6 (91) ◽  
pp. 88306-88314 ◽  
Author(s):  
Ping Yong ◽  
Yuejiao Yang ◽  
Zhiyong Wang ◽  
Liming Yang ◽  
Jie Chen
Keyword(s):  
Aqueous Solution ◽  
Triblock Copolymer ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Ph Sensitive ◽  
Reversible Addition ◽  
Subsequent Hydrolysis ◽  
Abc Triblock Copolymer

PNIPAM-b-PAA-b-P4VP (NAV), a thermo- and dual-pH-sensitive ABC triblock copolymer, was synthesized via sequential reversible addition–fragmentation chain transfer (RAFT) polymerization and subsequent hydrolysis.

scholarly journals Semi-Fluorinated Di and Triblock Copolymer Nano-Objects Prepared via RAFT Alcoholic Dispersion Polymerization (PISA)

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2502
Author(s):  
Gregoire Desnos ◽  
Adrien Rubio ◽  
Chaimaa Gomri ◽  
Mathias Gravelle ◽  
Vincent Ladmiral ◽  
...  
Keyword(s):  
Self Assembly ◽  
Triblock Copolymer ◽  
Dispersion Polymerization ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
The Self ◽  
The Core ◽  
Transmission Electron ◽  
Reversible Addition ◽  
Polymerization Conditions

A set of well-defined amphiphilic, semi-fluorinated di and triblock copolymers were synthesized via polymerization-induced self-assembly (PISA) under alcoholic dispersion polymerization conditions. This study investigates the influence of the length, nature and position of the solvophobic semi-fluorinated block. A poly(N,N-dimethylaminoethyl methacrylate) was used as the stabilizing block to prepare the di and tri block copolymer nano-objects via reversible addition-fragmentation chain transfer (RAFT) controlled dispersion polymerization at 70 °C in ethanol. Benzylmethacrylate (BzMA) and semi-fluorinated methacrylates and acrylates with 7 (heptafluorobutyl methacrylate (HFBMA)), 13 (heneicosafluorododecyl methacrylate (HCFDDMA)) and 21 (tridecafluorooctyl acrylate (TDFOA)) fluorine atoms were used as monomers for the core-forming blocks. The RAFT polymerization of these semi-fluorinated monomers was monitored by SEC and 1H NMR. The evolution of the self-assembled morphologies was investigated by transmission electron microscopy (TEM). The results demonstrate that the order of the blocks and the number of fluorine atoms influence the microphase segregation of the core-forming blocks and the final morphology of the nano-objects.

Self-Healing Hydrophobic POSS-functionalized Fluorinated Copolymer via RAFT Polymerization and dynamic Diels-Alder Reaction

2021 ◽  
Author(s):  
Siva Ponnupandian ◽  
Prantik Mondal ◽  
Thomas Becker ◽  
Richard Hoogenboom ◽  
Andrew B Lowe ◽  
...  
Keyword(s):  
Chain Transfer ◽  
Raft Polymerization ◽  
Alder Reaction ◽  
Diels Alder ◽  
Self Healing ◽  
Diels Alder Reaction ◽  
Reversible Addition

This investigation reports the preparation of a tailor-made copolymer of furfuryl methacrylate (FMA) and trifluoroethyl methacrylate (TFEMA) via reversible addition-fragmentation chain transfer (RAFT) polymerization. The furfuryl groups of the copolymer...

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