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RESEARCH PRODUCT

Polysarcosine-containing copolymers: Synthesis, characterization, self-assembly, and applications

Jun LingAlexander BirkeMatthias Barz

subject

chemistry.chemical_classificationSarcosinePolymers and PlasticsOrganic Chemistry02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistry0104 chemical sciencesPolyesterchemistry.chemical_compoundchemistryBromoacetic acidPolymerizationMaterials ChemistryCeramics and CompositesCopolymerSelf-assembly0210 nano-technologyEthylene glycol

description

Although the first polysarcosine (pSar) synthesis by Wesseley et al. was reported almost a century ago, it was only recently that pSar gained broader attention and is considered a potential alternative of poly(ethylene glycol) (PEG). In contrast to polyethers, such as PEG, pSar is a polypeptoid based on the amino acid sarcosine, i.e. N-methylated glycine. As a polymer, pSar combines PEG-like properties, e.g., excellent solubility in water, protein resistance, low cellular toxicity and a non-immunogenic character, while being based on endogenous material. Sarcosine can be obtained in a simple one-step reaction of bromoacetic acid and methylamine, easily transferred into the sarcosine N-(thio)carboxyanhydride and polymerized under living condition. This review provides a first comprehensive overview on pSar-containing block copolymers, which comprises of copolymers with polyesters, polyethers, polypeptides, polypeptoids, polyacrylates, others, as well as graft copolymers. The synthesis, characteristics and application of such polymers will be presented and discussed in detail. Finally, solution self-assembly and applications of pSar-containing block copolymers are reviewed underlining the enormous potential of this recently rediscovered polypeptoidic material. (C) 2018 Elsevier B.V. All rights reserved.

10.1016/j.progpolymsci.2018.01.002https://doi.org/10.1016/j.progpolymsci.2018.01.002