scholarly journals A Roadmap towards Successful Nanocapsule Synthesis via Vesicle Templated RAFT-Based Emulsion Polymerization

Polymers ◽  
2018 ◽  
Vol 10 (7) ◽  
pp. 774 ◽  
Author(s):  
Wendy Rusli ◽  
Alexander Jackson ◽  
Alexander van Herk

Vesicle templated emulsion polymerization is a special form of emulsion polymerization where the polymer is grown from the outside of the vesicle, leading to nanocapsules. Cost effective nanocapsules synthesis is in high demand due to phasing out of older methods for capsule synthesis. Although the first indications of this route being successful were published some 10 years ago, until now a thorough understanding of the parameters controlling the morphologies resulting from the template emulsion polymerization was lacking. Most often a mixture of different morphologies was obtained, ranging from solid particles to pro-trusion structures to nanocapsules. A high yield of nanocapsules was not achieved until now. In this paper, the influence of initial vesicle dispersion, choice of the Reversible Addition-Fragmentation chain Transfer (RAFT) species and oligomer, monomer and crosslinker have been investigated. It turns out that good initial vesicle dispersion, molecular control of the RAFT process, a not too hydrophobic monomer and some crosslinking is needed to result in high yield of nanocapsules. In previous work, the level of RAFT control was often suboptimal and not properly verified and although nanocapsules were shown, other morphologies were also present. We now believe we have a full understanding of vesicle templated nanocapsules synthesis, relevant to many applications.

RSC Advances ◽  
2016 ◽  
Vol 6 (42) ◽  
pp. 35621-35627 ◽  
Author(s):  
Ren He ◽  
Xiaoli Zhan ◽  
Qinghua Zhang ◽  
Fengqiu Chen

Reactive core–shell particles for epoxy toughening were synthesized via reversible addition–fragmentation chain transfer emulsion polymerization mediated by an amphiphilic macro-RAFT agent followed by core-crosslinking to increase stability.


Materials ◽  
2019 ◽  
Vol 12 (19) ◽  
pp. 3145 ◽  
Author(s):  
Katharina Nieswandt ◽  
Prokopios Georgopanos ◽  
Clarissa Abetz ◽  
Volkan Filiz ◽  
Volker Abetz

In this work, we present a novel synthetic route to diblock copolymers based on styrene and 3-vinylpyridine monomers. Surfactant-free water-based reversible addition–fragmentation chain transfer (RAFT) emulsion polymerization of styrene in the presence of the macroRAFT agent poly(3-vinylpyridine) (P3VP) is used to synthesize diblock copolymers with molecular weights of around 60 kDa. The proposed mechanism for the poly(3-vinylpyridine)-block-poly(styrene) (P3VP-b-PS) synthesis is the polymerization-induced self-assembly (PISA) which involves the in situ formation of well-defined micellar nanoscale objects consisting of a PS core and a stabilizing P3VP macroRAFT agent corona. The presented approach shows a well-controlled RAFT polymerization, allowing for the synthesis of diblock copolymers with high monomer conversion. The obtained diblock copolymers display microphase-separated structures according to their composition.


2019 ◽  
Vol 52 (8) ◽  
pp. 2965-2974 ◽  
Author(s):  
Thiago R. Guimarães ◽  
Murtaza Khan ◽  
Rhiannon P. Kuchel ◽  
Isabel C. Morrow ◽  
Hideto Minami ◽  
...  

2011 ◽  
Vol 64 (12) ◽  
pp. 1602 ◽  
Author(s):  
Yingkai Liu ◽  
Mei Li ◽  
Dengxu Wang ◽  
Jinshui Yao ◽  
Jianxing Shen ◽  
...  

A series of well defined semitelechelic and mid-functionalized poly(poly(ethylene glycol) methyl ether methacrylate)s (poly(PEGMA)s) were synthesized through reversible addition-fragmentation chain transfer (RAFT) polymerization using thiazolidine-2-thione-functionalized chain transfer agents (CTAs). The thiazolidine-2-thione group was located either at the end or in the middle of polymer chains depending on the different structural CTAs. All polymers were fully analyzed by 1H NMR spectroscopy and GPC, confirming their well-defined structures, such as predesigned molecular weights, narrow polydispersity indices, and high yield chain-end or chain-middle functionalization. The thiazolidine-2-thione functionality located at the end of or at the middle of the polymer chains can react with amine residues on protein surfaces, forming protein-polymer conjugates via amide linkages. The bioactivity of protein conjugates were subsequently tested using micrococcus lysodeikticus cell as substitute. The protein conjugations from the mid-functionalized polymer remained much more protein bioactivity comparing to their semitelechelic counterpart with similar molecular weights, indicating the steric hindrance of the mid-functionalized poly(PEGMA)s lead to the better selective conjugation to protein. The number of polymer chains on the protein surface was additionally evaluated by TNBS analysis, exhibiting that there are less mid-functionalized poly(PEGMA)s linked on the protein surface than the semitelechelic polymers, also supporting the hypothesis that the steric hindrance from branch-structural polymers results in the better reaction selectivity. This synthetic methodology is suitable for universal proteins, seeking a balance between the protein bioactivity and the protein protection by the covalent linkage with polymer, and exhibits promising potential for pharmaceutical protein conjugation.


2019 ◽  
Vol 68 (7) ◽  
pp. 1303-1314 ◽  
Author(s):  
Natalia S Serkhacheva ◽  
Nikolay I Prokopov ◽  
Elena V Chernikova ◽  
Elena Y Kozhunova ◽  
Inna O Lebedeva ◽  
...  

2006 ◽  
Vol 89 (8) ◽  
pp. 1641-1659 ◽  
Author(s):  
Bojana Apostolovic ◽  
Francesca Quattrini ◽  
Alessandro Butté ◽  
Giuseppe Storti ◽  
Massimo Morbidelli

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