A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in Water

P-tert-butyldihomooxacalix[4]arene is a well-known calix[4]arene analog in which one CH2 bridge is replaced by one -CH2OCH2- group. Thus, dihomooxacalix[4]arene has a slightly larger cavity than that of calix[4]arene and usually possesses a more flexible cone conformation, and the bridged oxygen ato...

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Main Authors: Hao Guo, Runmiao Zhang, Ying Han, Jin Wang, Chaoguo Yan
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Chemistry
Subjects:
gel
Online Access:https://www.frontiersin.org/article/10.3389/fchem.2020.00033/full
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spelling doaj-6a9c305fd7694a1eaf2abbd153f31c292020-11-25T03:36:32ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462020-02-01810.3389/fchem.2020.00033513189A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in WaterHao Guo0Hao Guo1Runmiao Zhang2Runmiao Zhang3Ying Han4Jin Wang5Chaoguo Yan6School of Chemistry and Chemical Engineer, Yangzhou University, Yangzhou, ChinaSchool of Chemistry and Chemical Engineer, Nantong University, Nantong, ChinaSchool of Chemistry and Chemical Engineer, Yangzhou University, Yangzhou, ChinaSchool of Chemistry and Chemical Engineer, Nantong University, Nantong, ChinaSchool of Chemistry and Chemical Engineer, Yangzhou University, Yangzhou, ChinaSchool of Chemistry and Chemical Engineer, Nantong University, Nantong, ChinaSchool of Chemistry and Chemical Engineer, Yangzhou University, Yangzhou, ChinaP-tert-butyldihomooxacalix[4]arene is a well-known calix[4]arene analog in which one CH2 bridge is replaced by one -CH2OCH2- group. Thus, dihomooxacalix[4]arene has a slightly larger cavity than that of calix[4]arene and usually possesses a more flexible cone conformation, and the bridged oxygen atom might provide additional binding sites. Here, we synthesized a new functional p-tert-butyldihomooxacalix[4]arene 1 through Ugi reaction with good yield (70%), starting from condensed p-tert-butyldihomooxacalix[4]arene O-alkoxy–substituted benzaldehydes, benzoic acid, benzylamine, and cyclohexyl isocyanide. Proton nuclear magnetic resonance spectroscopy (1H NMR), 13C NMR, IR, and diffusion-ordered 1H NMR spectroscopy (DOSY) methods were used to characterize the structure of 1. Then soft gel was prepared by adding 1 into cyclohexane directly. It shows remarkable thermoreversibility and can be demonstrated for several cycles. As is revealed by scanning electron microscopy (SEM) images, xerogel showed highly interconnected and homogeneous porous network structures, and hence, the gel is suitable for storage and controlled release.https://www.frontiersin.org/article/10.3389/fchem.2020.00033/fullcalixarenesgelcontrolled releasemacrocyclic compoundsUgi reaction
collection DOAJ
language English
format Article
sources DOAJ
author Hao Guo
Hao Guo
Runmiao Zhang
Runmiao Zhang
Ying Han
Jin Wang
Chaoguo Yan
spellingShingle Hao Guo
Hao Guo
Runmiao Zhang
Runmiao Zhang
Ying Han
Jin Wang
Chaoguo Yan
A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in Water
Frontiers in Chemistry
calixarenes
gel
controlled release
macrocyclic compounds
Ugi reaction
author_facet Hao Guo
Hao Guo
Runmiao Zhang
Runmiao Zhang
Ying Han
Jin Wang
Chaoguo Yan
author_sort Hao Guo
title A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in Water
title_short A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in Water
title_full A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in Water
title_fullStr A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in Water
title_full_unstemmed A p-tert-Butyldihomooxacalix[4]arene Based Soft Gel for Sustained Drug Release in Water
title_sort p-tert-butyldihomooxacalix[4]arene based soft gel for sustained drug release in water
publisher Frontiers Media S.A.
series Frontiers in Chemistry
issn 2296-2646
publishDate 2020-02-01
description P-tert-butyldihomooxacalix[4]arene is a well-known calix[4]arene analog in which one CH2 bridge is replaced by one -CH2OCH2- group. Thus, dihomooxacalix[4]arene has a slightly larger cavity than that of calix[4]arene and usually possesses a more flexible cone conformation, and the bridged oxygen atom might provide additional binding sites. Here, we synthesized a new functional p-tert-butyldihomooxacalix[4]arene 1 through Ugi reaction with good yield (70%), starting from condensed p-tert-butyldihomooxacalix[4]arene O-alkoxy–substituted benzaldehydes, benzoic acid, benzylamine, and cyclohexyl isocyanide. Proton nuclear magnetic resonance spectroscopy (1H NMR), 13C NMR, IR, and diffusion-ordered 1H NMR spectroscopy (DOSY) methods were used to characterize the structure of 1. Then soft gel was prepared by adding 1 into cyclohexane directly. It shows remarkable thermoreversibility and can be demonstrated for several cycles. As is revealed by scanning electron microscopy (SEM) images, xerogel showed highly interconnected and homogeneous porous network structures, and hence, the gel is suitable for storage and controlled release.
topic calixarenes
gel
controlled release
macrocyclic compounds
Ugi reaction
url https://www.frontiersin.org/article/10.3389/fchem.2020.00033/full
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