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全两性离子功能化树枝状大分子的设计、合成与表征

Design, Synthesis, and Characterization of Fully Zwitterionic, Functionalized Dendrimers.

作者信息

Roeven Esther, Scheres Luc, Smulders Maarten M J, Zuilhof Han

机构信息

Laboratory of Organic Chemistry, Wageningen University, Stippeneng 4, 6708 WE Wageningen, The Netherlands.

Surfix BV, Bronland 12 B-1, 6708 WH Wageningen, The Netherlands.

出版信息

ACS Omega. 2019 Feb 28;4(2):3000-3011. doi: 10.1021/acsomega.8b03521. Epub 2019 Feb 11.

Abstract

Dendrimers are interesting candidates for various applications because of the high level of control over their architecture, the presence of internal cavities, and the possibility for multivalent interactions. More specifically, zwitterionic dendrimers modified with an equal number of oppositely charged groups have found use in in vivo biomedical applications. However, the design and control over the synthesis of these dendrimers remains challenging, in particular with respect to achieving full modification of the dendrimer. In this work, we show the design and subsequent synthesis of dendrimers that are highly charged while having zero net charge, that is zwitterionic dendrimers that are potential candidates for biomedical applications. First, we designed and fully optimized the synthesis of charge-neutral carboxybetaine and sulfobetaine zwitterionic dendrimers. Following their synthesis, the various zwitterionic dendrimers were extensively characterized. In this study, we also report for the first time the use of X-ray photoelectron spectroscopy as an easy-to-use and quantitative tool for the compositional analysis of this type of macromolecules that can complement techniques such as nuclear magnetic resonance and gel permeation chromatography. Finally, we designed and synthesized zwitterionic dendrimers that contain a variable number of alkyne and azide groups that allow straightforward (bio)functionalization via click chemistry.

摘要

树枝状大分子因其在结构控制、内部空腔的存在以及多价相互作用的可能性等方面具有高度可控性,而成为各种应用中颇具吸引力的候选材料。更具体地说,带有等量相反电荷基团修饰的两性离子树枝状大分子已在体内生物医学应用中得到应用。然而,这些树枝状大分子的设计和合成控制仍然具有挑战性,特别是在实现树枝状大分子的完全修饰方面。在这项工作中,我们展示了设计并随后合成的带高电荷但净电荷为零的树枝状大分子,即两性离子树枝状大分子,它们是生物医学应用的潜在候选材料。首先,我们设计并完全优化了电荷中性的羧基甜菜碱和磺基甜菜碱两性离子树枝状大分子的合成。合成之后,对各种两性离子树枝状大分子进行了广泛表征。在本研究中,我们还首次报道了使用X射线光电子能谱作为一种易于使用的定量工具,用于此类大分子的组成分析,它可以补充核磁共振和凝胶渗透色谱等技术。最后,我们设计并合成了含有可变数量炔基和叠氮基的两性离子树枝状大分子,这些基团允许通过点击化学进行直接的(生物)功能化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb9c/6647342/930dc4c554b3/ao-2018-035213_0006.jpg

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