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Crosslinked p(MMA) particles by RAFT emulsion polymerisation: tuning size and stability

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Crosslinked p(MMA) particles by RAFT emulsion polymerisation: tuning size and stability. / Marsden, Catherine J.; Breen, Colum; Tinkler, James D. et al.
In: Polymer Chemistry, Vol. 13, No. 28, 28.07.2022, p. 4124-4135.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Marsden, CJ, Breen, C, Tinkler, JD, Berki, TR, Lester, DW, Martinelli, J, Tei, L, Butler, SJ & Willcock, H 2022, 'Crosslinked p(MMA) particles by RAFT emulsion polymerisation: tuning size and stability', Polymer Chemistry, vol. 13, no. 28, pp. 4124-4135. https://doi.org/10.1039/D2PY00337F

APA

Marsden, C. J., Breen, C., Tinkler, J. D., Berki, T. R., Lester, D. W., Martinelli, J., Tei, L., Butler, S. J., & Willcock, H. (2022). Crosslinked p(MMA) particles by RAFT emulsion polymerisation: tuning size and stability. Polymer Chemistry, 13(28), 4124-4135. https://doi.org/10.1039/D2PY00337F

Vancouver

Marsden CJ, Breen C, Tinkler JD, Berki TR, Lester DW, Martinelli J et al. Crosslinked p(MMA) particles by RAFT emulsion polymerisation: tuning size and stability. Polymer Chemistry. 2022 Jul 28;13(28):4124-4135. Epub 2022 Jun 1. doi: 10.1039/D2PY00337F

Author

Marsden, Catherine J. ; Breen, Colum ; Tinkler, James D. et al. / Crosslinked p(MMA) particles by RAFT emulsion polymerisation : tuning size and stability. In: Polymer Chemistry. 2022 ; Vol. 13, No. 28. pp. 4124-4135.

Bibtex

@article{c682c5e0131a47b09d553f09c0b73c7c,
title = "Crosslinked p(MMA) particles by RAFT emulsion polymerisation: tuning size and stability",
abstract = "The controlled synthesis of amphiphilic di-block copolymers allows a large array of nanostructures to be created, including block copolymer particles, which have proved valuable for biomedical applications. Despite progress in targeting specific block copolymer architectures, control over the size and stability of spherical particles is less well explored. Here, we report the use of RAFT emulsion polymerisation to synthesise a library of p(MMA) particles, crosslinked with ethylene glycol dimethacrylate and stabilised by brush-like poly(ethylene glycol)-based polymers. We successfully synthesised a range of block copolymer particles, offering stability up to p(MMA)1000, with DLS reporting stable particle diameters of 33–176 nm and PDI < 0.2. DLS and AFM studies showed a general increase in particle diameter with increasing amounts of p(MMA). The use of a PEG methacrylate monomer with a methyl ether end group resulted in more well defined and stable particles than those with hydroxyl end groups. The copolymerisation of a suitably functionalized Gd(III) complex into the shell of the spherical p(MMA) particles resulted in Gd-loaded particles that were investigated in detail by 1H NMR relaxometry, demonstrating that the Gd complex was successfully incorporated into the particles. This study will inform the synthesis of core–shell particles with optimised stability and targeted sizes, and show a simple method to incorporate a molecular sensor, generating a macromolecular imaging agent.",
keywords = "Polymer, Chemistry, Macromolecular, MRI, Block copolymer particle, Magnetic resonance",
author = "Marsden, {Catherine J.} and Colum Breen and Tinkler, {James D.} and Berki, {Thomas R.} and Lester, {Daniel W.} and Jonathan Martinelli and Lorenzo Tei and Butler, {Stephen J.} and Helen Willcock",
year = "2022",
month = jul,
day = "28",
doi = "10.1039/D2PY00337F",
language = "English",
volume = "13",
pages = "4124--4135",
journal = "Polymer Chemistry",
issn = "1759-9954",
publisher = "Royal Society of Chemistry",
number = "28",

}

RIS

TY - JOUR

T1 - Crosslinked p(MMA) particles by RAFT emulsion polymerisation

T2 - tuning size and stability

AU - Marsden, Catherine J.

AU - Breen, Colum

AU - Tinkler, James D.

AU - Berki, Thomas R.

AU - Lester, Daniel W.

AU - Martinelli, Jonathan

AU - Tei, Lorenzo

AU - Butler, Stephen J.

AU - Willcock, Helen

PY - 2022/7/28

Y1 - 2022/7/28

N2 - The controlled synthesis of amphiphilic di-block copolymers allows a large array of nanostructures to be created, including block copolymer particles, which have proved valuable for biomedical applications. Despite progress in targeting specific block copolymer architectures, control over the size and stability of spherical particles is less well explored. Here, we report the use of RAFT emulsion polymerisation to synthesise a library of p(MMA) particles, crosslinked with ethylene glycol dimethacrylate and stabilised by brush-like poly(ethylene glycol)-based polymers. We successfully synthesised a range of block copolymer particles, offering stability up to p(MMA)1000, with DLS reporting stable particle diameters of 33–176 nm and PDI < 0.2. DLS and AFM studies showed a general increase in particle diameter with increasing amounts of p(MMA). The use of a PEG methacrylate monomer with a methyl ether end group resulted in more well defined and stable particles than those with hydroxyl end groups. The copolymerisation of a suitably functionalized Gd(III) complex into the shell of the spherical p(MMA) particles resulted in Gd-loaded particles that were investigated in detail by 1H NMR relaxometry, demonstrating that the Gd complex was successfully incorporated into the particles. This study will inform the synthesis of core–shell particles with optimised stability and targeted sizes, and show a simple method to incorporate a molecular sensor, generating a macromolecular imaging agent.

AB - The controlled synthesis of amphiphilic di-block copolymers allows a large array of nanostructures to be created, including block copolymer particles, which have proved valuable for biomedical applications. Despite progress in targeting specific block copolymer architectures, control over the size and stability of spherical particles is less well explored. Here, we report the use of RAFT emulsion polymerisation to synthesise a library of p(MMA) particles, crosslinked with ethylene glycol dimethacrylate and stabilised by brush-like poly(ethylene glycol)-based polymers. We successfully synthesised a range of block copolymer particles, offering stability up to p(MMA)1000, with DLS reporting stable particle diameters of 33–176 nm and PDI < 0.2. DLS and AFM studies showed a general increase in particle diameter with increasing amounts of p(MMA). The use of a PEG methacrylate monomer with a methyl ether end group resulted in more well defined and stable particles than those with hydroxyl end groups. The copolymerisation of a suitably functionalized Gd(III) complex into the shell of the spherical p(MMA) particles resulted in Gd-loaded particles that were investigated in detail by 1H NMR relaxometry, demonstrating that the Gd complex was successfully incorporated into the particles. This study will inform the synthesis of core–shell particles with optimised stability and targeted sizes, and show a simple method to incorporate a molecular sensor, generating a macromolecular imaging agent.

KW - Polymer

KW - Chemistry

KW - Macromolecular

KW - MRI

KW - Block copolymer particle

KW - Magnetic resonance

U2 - 10.1039/D2PY00337F

DO - 10.1039/D2PY00337F

M3 - Journal article

VL - 13

SP - 4124

EP - 4135

JO - Polymer Chemistry

JF - Polymer Chemistry

SN - 1759-9954

IS - 28

ER -