TY - JOUR
T1 - Forced gradient copolymerisation
T2 - a simplified approach for polymerisation-induced self-assembly
AU - Xu, Sihao
AU - Corrigan, Nathaniel
AU - Boyer, Cyrille
PY - 2021/1
Y1 - 2021/1
N2 - In this work, a novel and versatile gradient copolymerisation approach to simplify polymeric nanoparticle synthesis through polymerisation-induced self-assembly (PISA) is reported. In contrast with the commonly performed two-step PISA process, which involves chain-extension of a pre-synthesised stabiliser (or solvophilic block), this work demonstrates a one pot PISA approach via the formation of gradient copolymers through a gradual injection of the core-forming monomer in the presence of a solvophilic monomer. To demonstrate this concept, two model PISA systems were tested using a methacrylate monomer pair and an acrylamide pair. PISA using dimethylacrylamide (DMA) and diacetone acrylamide (DAAm) was first established to form a range of nanoparticle morphologies (spheres and worms), and importantly, a pure worm phase was observed without the addition of a co-solvent or a second solvophilic monomer during the polymerisation of the core-forming monomer. To demonstrate the gradient approach can be applied to other PISA monomer pairs, this methodology was applied to a system using oligo(ethylene glycol)methyl ether methacrylate (OEGMA300) and 2-hydroxypropyl methacrylate (HPMA) as monomers. PISA of this monomer pair resulted in the formation of nanoparticles with various morphologies, including spheres, worms and vesicles. More interestingly, the nanoparticles formed using these gradient copolymers presented thermoresponsive behaviour, exhibiting a sphere-to-worm transition with an increase in temperature from 25 °C to 40 °C. Thus, this facile gradient copolymerisation approach was shown to simplify the PISA process into a single step approach with easily tuneable solvophilic block length and copolymer composition, and additionally provide nanoparticle structures that afford unique properties.
AB - In this work, a novel and versatile gradient copolymerisation approach to simplify polymeric nanoparticle synthesis through polymerisation-induced self-assembly (PISA) is reported. In contrast with the commonly performed two-step PISA process, which involves chain-extension of a pre-synthesised stabiliser (or solvophilic block), this work demonstrates a one pot PISA approach via the formation of gradient copolymers through a gradual injection of the core-forming monomer in the presence of a solvophilic monomer. To demonstrate this concept, two model PISA systems were tested using a methacrylate monomer pair and an acrylamide pair. PISA using dimethylacrylamide (DMA) and diacetone acrylamide (DAAm) was first established to form a range of nanoparticle morphologies (spheres and worms), and importantly, a pure worm phase was observed without the addition of a co-solvent or a second solvophilic monomer during the polymerisation of the core-forming monomer. To demonstrate the gradient approach can be applied to other PISA monomer pairs, this methodology was applied to a system using oligo(ethylene glycol)methyl ether methacrylate (OEGMA300) and 2-hydroxypropyl methacrylate (HPMA) as monomers. PISA of this monomer pair resulted in the formation of nanoparticles with various morphologies, including spheres, worms and vesicles. More interestingly, the nanoparticles formed using these gradient copolymers presented thermoresponsive behaviour, exhibiting a sphere-to-worm transition with an increase in temperature from 25 °C to 40 °C. Thus, this facile gradient copolymerisation approach was shown to simplify the PISA process into a single step approach with easily tuneable solvophilic block length and copolymer composition, and additionally provide nanoparticle structures that afford unique properties.
UR - http://www.scopus.com/inward/record.url?scp=85099035272&partnerID=8YFLogxK
UR - https://go.openathens.net/redirector/westernsydney.edu.au?url=https://doi.org/10.1039/d0py00889c
U2 - 10.1039/d0py00889c
DO - 10.1039/d0py00889c
M3 - Article
AN - SCOPUS:85099035272
SN - 1759-9954
VL - 12
SP - 57
EP - 68
JO - Polymer Chemistry
JF - Polymer Chemistry
IS - 1
ER -