Issue 25, 2019

Dual acid-responsive bola-type supramolecular vesicles for efficient intracellular anticancer drug delivery

Abstract

Dual acid-responsive bola-type supramolecular vesicles have been successfully constructed for efficient intracellular anticancer drug delivery, which are fabricated by the complexation between a water-soluble pillar[5]arene (WP5) and an acid-sensitive guest molecule (G) containing the 2,4,8,10-tetraoxaspiro[5.5]undecane moiety. Compared with the control system that only has single pH-responsiveness of WP5, the obtained dual acid-responsive supramolecular vesicles exhibit much faster drug release efficiency under the acid microenvironment of cancer cells. Moreover, cytotoxicity experiments confirm that the doxorubicin (DOX)-loaded supramolecular vesicles can not only obviously enhance the anticancer efficiency of free DOX for tumor cells, but also remarkably reduce the side effects on normal cells, suggesting their potential applications in cancer therapy.

Graphical abstract: Dual acid-responsive bola-type supramolecular vesicles for efficient intracellular anticancer drug delivery

Supplementary files

Article information

Article type
Communication
Submitted
21 Mar 2019
Accepted
31 May 2019
First published
05 Jun 2019

J. Mater. Chem. B, 2019,7, 3944-3949

Dual acid-responsive bola-type supramolecular vesicles for efficient intracellular anticancer drug delivery

G. Sun, Z. He, M. Hao, M. Zuo, Z. Xu, X. Hu, J. Zhu and L. Wang, J. Mater. Chem. B, 2019, 7, 3944 DOI: 10.1039/C9TB00555B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements