Hydrophobicity of surface-immobilised molecules influences architectures formed via interfacial self-assembly of nucleoside-based gelators

被引：7

作者：

Angelerou, Maria Galini Faidra ^{[1
]}

Yang, Bin ^{[1
]}

Arnold, Thomas ^{[2
,3
,4
,5
]}

Rawle, Jonathan ^{[2
]}

Marlow, Maria ^{[1
]}

Zelzer, Mischa ^{[1
]}

机构：

[1] Univ Nottingham, Dept Pharm, Nottingham NG2 7RD, England

[2] Diamond Light Source Ltd, Harwell Sci & Innovat Campus, Didcot OX11 0DE, Oxon, England

[3] European Spallat Source ERIC, POB 176, SE-22100 Lund, Sweden

[4] STFC, Rutherford Appleton Lab, Didcot OX11 0QX, Oxon, England

[5] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England

来源：

SOFT MATTER | 2018年 / 14卷 / 48期

基金：

英国工程与自然科学研究理事会;

关键词：

SUPRAMOLECULAR GELS; PEPTIDE AMPHIPHILES; DRUG-DELIVERY;

D O I：

10.1039/c8sm01868e

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

Surface-mediated self-assembly has potential in biomaterial development but underlying rules governing surface-gelator interactions are poorly understood. Here, we correlate surface properties with structural characterization data of nucleoside-based gels obtained by GISAXS and GIWAXS and find that hydrophobicity descriptors (logP, polar surface area, aromaticity) are key predictors for the gel structures formed.

引用

页码：9851 / 9855

页数：5

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