磷脂缀合物:分子内π-阳离子络合物的形成。

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Valery P Shendrikov, Erik F Kot, Kirill I Makrinsky, Abdulilah Ece, Ivan A Boldyrev
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引用次数: 0

摘要

磷脂偶联物由功能不同的分子类别组成:磷脂药物偶联物、荧光脂质探针和脂质分子马达。所有这些共轭物都是带有一个官能团的分子——一个药物、一个荧光团或一个附着在磷脂上的分子马达。偶联需要将官能团结合到脂质体或脂质纳米颗粒的脂质双层中,从而调节药物的效果或为脂质体带来新的功能。利用核磁共振波谱和量子化学计算,我们发现磷脂缀合物可以在磷脂酰胆碱的季铵盐基团和共轭部分的芳环之间形成分子内π-阳离子配合物。我们还报道了如何避免π-阳离子络合物的形成。如果芳香基团与胆碱基团之间的连接体足够长,则不会形成π-阳离子配合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phospholipid conjugates: formation of the intramolecular π-cation complex.

Phospholipid conjugates consist of functionally different classes of molecules: phospholipid drug conjugates, fluorescent lipid probes and lipid molecular motors. All these conjugates are molecules that bear a functional group- a drug, a fluorophore or a molecular motor attached to the phospholipid. The conjugation is needed to incorporate a functional group into the lipid bilayer of liposome or lipid nanoparticle and thus, either modulate the effect of the drug or bring a new function to the liposome. Here, using NMR spectroscopy and quantum chemistry calculations, we show that phospholipid conjugates can form intramolecular π-cation complexes between quaternary ammonium group of the phosphatidylcholine and aromatic ring of the conjugated moiety. We also report on how to avoid the π-cation complex formation. If the linker between the aromatic moiety and the choline group is long enough the formation of π-cation complex is not observed.

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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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