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Design, Preparation, and Characterization of Novel Calix[4]arene Bioactive Carrier for Antitumor Drug Delivery.


ABSTRACT: An amphiphilic and bioactive calix[4]arene derivative 8 (CA) is designed and successfully synthesized from tert-butyl calix[4] arene 1 by sequential inverse F-C alkylation, nitration, O-alkylation, esterification, aminolysis, reduction, and acylation reaction. The blank micelles of FA-CA and doxorubicin (DOX) loaded micelles FA-CA-DOX are prepared subsequently undergoing self-assembly and dialysis of CA and DSPE-PEG2000-FA. The drug release kinetics curve of the encapsulated-DOX micelle demonstrates a rapid release under mild conditions, indicating the good pH-responsive ability. Furthermore, the cytotoxicity of DOX-loaded micelle respect to the blank micelle against seven different human carcinoma (A549, HeLa, HepG2, HCT116, MCF-7, MDA-MB231, and SW480) cells has been also investigated. The results confirm the more significant inhibitory effect of DOX-loaded micelle than those of DOX and the blank micelles. The CDI calculations show a synergistic effect between blank micelles and DOX in inducing tumor cell death. In conclusion, FA-CA micelles reported in this work was a promising drug delivery vehicle for tumor targeting therapy.

SUBMITTER: An L 

PROVIDER: S-EPMC6855266 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Design, Preparation, and Characterization of Novel Calix[4]arene Bioactive Carrier for Antitumor Drug Delivery.

An Lin L   Wang Jia-Wei JW   Liu Jia-Dong JD   Zhao Zi-Ming ZM   Song Yuan-Jian YJ  

Frontiers in chemistry 20191107


An amphiphilic and bioactive calix[4]arene derivative <b>8 (CA)</b> is designed and successfully synthesized from <i>tert</i>-butyl calix[4] arene <b>1</b> by sequential inverse F-C alkylation, nitration, O-alkylation, esterification, aminolysis, reduction, and acylation reaction. The blank micelles of <b>FA-CA</b> and doxorubicin (DOX) loaded micelles <b>FA-CA-DOX</b> are prepared subsequently undergoing self-assembly and dialysis of <b>CA</b> and DSPE-PEG<sub>2000</sub>-FA. The drug release ki  ...[more]

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