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氟化隐形聚(ε-己内酯)纳米载体的设计

Design of fluorinated stealth poly(ε-caprolactone) nanocarriers.

作者信息

Bona Beatrice Lucia, Lagarrigue Prescillia, Chirizzi Cristina, Espinoza Maria Isabel Martinez, Pipino Christian, Metrangolo Pierangelo, Cellesi Francesco, Baldelli Bombelli Francesca

机构信息

SupraBioNanoLab, Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Milano 20131, Italy.

SupraBioNanoLab, Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Milano 20131, Italy; Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Milano 20131, Italy.

出版信息

Colloids Surf B Biointerfaces. 2024 Feb;234:113730. doi: 10.1016/j.colsurfb.2023.113730. Epub 2023 Dec 26.

Abstract

The covalent functionalization of polymers with fluorinated moieties represents a promising strategy for the development of multimodal systems. Moreover, polymer fluorination often endows the resulting nanocarriers with improved colloidal stability in the biological environment. In this work, we developed fluorinated pegylated (PEG) biodegradable poly(ε-caprolactone) (PCL) drug nanocarriers showing both high colloidal stability and stealth properties, as well as being (F)-Nuclear Magnetic Resonance (NMR) detectable. The optimized nanocarriers were obtained mixing a PEG-PCL block copolymer with a nonafluoro-functionalized PCL polymer. The role of PEGylation and fluorination on self-assembly and colloidal behavior of the obtained nanoparticles (NPs) was investigated, as well as their respective role on stealth properties and colloidal stability. To prove the feasibility of the developed NPs as potential F NMR detectable drug delivery systems, a hydrophobic drug was successfully encapsulated, and the maintenance of the relevant F NMR properties evaluated. Drug-loaded fluorinated NPs still retained a sharp and intense F NMR signal and good relaxivity parameters (i.e., T and T relaxation times) in water, which were not impaired by drug encapsulation.

摘要

聚合物与含氟部分的共价功能化是开发多模态系统的一种有前景的策略。此外,聚合物氟化通常会使所得纳米载体在生物环境中具有更好的胶体稳定性。在这项工作中,我们开发了氟化聚乙二醇化(PEG)可生物降解聚(ε-己内酯)(PCL)药物纳米载体,其既具有高胶体稳定性和隐身特性,又可通过(F)-核磁共振(NMR)检测到。通过将PEG-PCL嵌段共聚物与九氟功能化PCL聚合物混合获得了优化的纳米载体。研究了聚乙二醇化和氟化对所得纳米颗粒(NPs)自组装和胶体行为的作用,以及它们在隐身特性和胶体稳定性方面各自的作用。为了证明所开发的NPs作为潜在的F NMR可检测药物递送系统的可行性,成功封装了一种疏水性药物,并评估了相关F NMR特性的维持情况。载药氟化NPs在水中仍保留尖锐且强烈的F NMR信号和良好的弛豫参数(即T和T弛豫时间),药物封装并未损害这些参数。

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