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Poly(Pentafluorophenyl Methacrylate)-Based Nano-Objects Developed by Photo-PISA as Scaffolds for Post-Polymerization Functionalization
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Georgiou, Panagiotis G.
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Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
Univ Warwick, Dept Chem, Gibbet Hill Rd, Coventry CV4 7AL, W Midlands, England Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England

Varlas, Spyridon
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Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England

Jones, Joseph R.
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Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England

Arno, Maria C.
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Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England

Foster, Jeffrey C.
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Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England

O'Reilly, Rachel K.
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Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
机构:
[1] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
[2] Univ Warwick, Dept Chem, Gibbet Hill Rd, Coventry CV4 7AL, W Midlands, England
基金:
欧盟地平线“2020”;
英国工程与自然科学研究理事会;
关键词:
activated esters;
nano-objects;
polymer functionalization;
polymerization-induced self-assembly (PISA);
reversible addition-fragmentation chain-transfer polymerization (RAFT);
RESPONSIVE NANOPARTICLES;
RAFT POLYMERIZATION;
BLOCK-COPOLYMERS;
DELIVERY;
POLYMERS;
PH;
TEMPERATURE;
MICELLES;
D O I:
10.1002/marc.201800460
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
The preparation of a functional fluorine-containing block copolymer using reversible addition-fragmentation chain-transfer dispersion polymerization in DMSO as a "platform/scaffold" is explored. The nanostructures, comprised of poly(ethyleneglycol)-b-poly(pentafluorophenyl methacrylate) or PEG-b-P(PFMA), are formulated via photo-initiated polymerization-induced self-assembly (PISA) followed by post-polymerization modification using different primary amines. A combination of light scattering and microscopy techniques are used to characterize the resulting morphologies. It is found that upon varying the degree of polymerization of the core-forming block of PFMA, only uniform spheres (with textured surfaces) are obtained. These nanostructures are subsequently modified by cross-linking using a non-responsive and a redox-responsive diamine, thus imparting stability to the particles in water. In response to intracellular glutathione (GSH) concentration, destabilization of the micelles occurs as evidenced by dynamic light scattering. The well-defined size, inherent reactivity of the nanoparticles toward nucleophiles, and GSH-responsiveness of the nanospheres make them ideal scaffolds for drug delivery to intracellular compartments with reductive environments.
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Max Planck Inst Colloids & Interfaces, Dept Biomol Syst, D-14424 Potsdam, Germany Humboldt Univ, Dept Chem, Lab Organ Synth Funct Syst, D-12489 Berlin, Germany

Seeberger, Peter H.
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Max Planck Inst Colloids & Interfaces, Dept Biomol Syst, D-14424 Potsdam, Germany
Free Univ Berlin, Inst Chem & Biochem, Dept Biol Chem & Pharm, D-14195 Berlin, Germany Humboldt Univ, Dept Chem, Lab Organ Synth Funct Syst, D-12489 Berlin, Germany

Borner, Hans G.
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Humboldt Univ, Dept Chem, Lab Organ Synth Funct Syst, D-12489 Berlin, Germany Humboldt Univ, Dept Chem, Lab Organ Synth Funct Syst, D-12489 Berlin, Germany