4.7 Article

Nitrile-Functionalized Poly(2-oxazoline)s as a Versatile Platform for the Development of Polymer Therapeutics

期刊

BIOMACROMOLECULES
卷 22, 期 11, 页码 4618-4632

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.1c00923

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资金

  1. ARC Centre of Excellence in Convergent Bio-Nano Science and Technology [CE140100036]
  2. Australian Research Council (ARC) [FT190100572]
  3. Alexander von Humboldt Foundation (Feodor-Lynen fellowship)
  4. Monash Graduate Scholarship
  5. Australian Research Council [FT190100572] Funding Source: Australian Research Council

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This article introduces a novel nitrile-functionalized 2-oxazoline monomer and demonstrates its compatibility with cationic ring-opening polymerization, showcasing the versatility of nitrile-functionalized poly(2-oxazoline)s. These polymers are shown to efficiently encapsulate and release drugs such as curcumin, as well as release nitric oxide intracellularly, indicating their potential in biomedical applications. The study highlights the promising and robust platform of nitrile-functionalized poly(2-oxazoline)s for polymer therapeutics design in various fields.
In recent years, polymers bearing reactive groups have received significant interest for biomedical applications. Numerous functional polymer platforms have been introduced, which allow for the preparation of materials with tailored properties via post-polymerization modifications. However, because of their reactivity, many functional groups are not compatible with the initial polymerization. The nitrile group is a highly interesting and relatively inert functionality that has mainly received attention in radical polymerizations. In this Article, a nitrile-functionalized 2-oxazoline monomer (2-(4-nitrile-butyl)-2-oxazoline, BuNiOx) is introduced, and its compatibility with the cationic ring-opening polymerization is demonstrated. Subsequently, the versatility of nitrile-functionalized poly(2-oxazoline)s (POx) is presented. To this end, diverse (co)polymers are synthesized and characterized by nuclear resonance spectroscopy, size-exclusion chromatography, and mass spectrometry. Amphiphilic block copolymers are shown to efficiently encapsulate the hydrophobic drug curcumin (CUR) in aqueous solution, and the anti-inflammatory effect of the CUR-containing nanostructures is presented in BV-2 microglia. Furthermore, the availability of the BuNiOx repeating units for post-polymerization modifications with hydroxylamine to yield amidoxime (AO)-functionalized POx is demonstrated. These AO-containing POx were successfully applied for the complexation of Fe(III) in a quantitative manner. In addition, AO-functionalized POx were shown to release nitric oxide intracellularly in BV-2 microglia. Thus nitrile-functionalized POx represent a promising and robust platform for the design of polymer therapeutics for a wide range of applications.

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