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Hybrid Molecular Container Based on Glycoluril and Triptycene: Synthesis, Binding Properties, and Triggered Release.

Authors :
Liu, Wenjin
Lu, Xiaoyong
Xue, Weijian
Samanta, Soumen K.
Zavalij, Peter Y.
Meng, Zihui
Isaacs, Lyle
Source :
Chemistry - A European Journal. 9/20/2018, Vol. 24 Issue 53, p14101-14110. 10p.
Publication Year :
2018

Abstract

Abstract: We designed and synthesized a “hybrid” molecular container 1, which is structurally related to both cucurbit[n]uril (CB[n]) and pillar[n]arene type receptors. Receptor 1 was fully characterized by 1H NMR, 13C NMR, IR, MS and X‐ray single crystal diffraction. The self‐association behavior, host–guest recognition properties of 1, and the [salt] dependence of Ka were investigated in detail by 1H NMR and isothermal titration calorimetry (ITC). Optical transmittance and TEM measurements provide strong evidence that receptor 1 undergoes co‐assemble with amphiphilic guest C10 in water to form supramolecular bilayer vesicles (diameter 25.6±2.7 nm, wall thickness ≈3.5 nm) that can encapsulate the hydrophilic anticancer drug doxorubicin (DOX) and the hydrophobic dye Nile red (NR). The release of encapsulated DOX or NR from the vesicles can be triggered by hexamethonium (8 c) or spermine (10) which leads to the disruption of the supramolecular vesicles. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09476539
Volume :
24
Issue :
53
Database :
Academic Search Index
Journal :
Chemistry - A European Journal
Publication Type :
Academic Journal
Accession number :
131909580
Full Text :
https://doi.org/10.1002/chem.201802981