Issue 39, 2022

A photo-responsive fluorescent amphiphile for target-specific and image-guided drug delivery applications

Abstract

Multifunctional drug delivery systems are the centerpiece of effective chemotherapeutic strategies. Herein, we report the synthesis of an acetazolamide-linked cyanine-3-based NIR-responsive fluorescent macrocyclic amphiphile that self-assembled into spherical nanostructures in the aqueous medium via a J-aggregation pattern. The amphiphile shows various favorable properties of lipids. The photocleavage of the strained dioxacycloundecine ring induces spherical to nanotubular self-assembly with concomitant release of an encapsulated anticancer drug, doxorubicin (Dox), in a controlled manner. The CA-IX targeted amphiphile also showed lower cytotoxicity, effective cellular uptake, and Dox delivery to the model carcinoma cells.

Graphical abstract: A photo-responsive fluorescent amphiphile for target-specific and image-guided drug delivery applications

Supplementary files

Article information

Article type
Paper
Submitted
24 Jul 2022
Accepted
12 Sep 2022
First published
13 Sep 2022

Org. Biomol. Chem., 2022,20, 7803-7813

A photo-responsive fluorescent amphiphile for target-specific and image-guided drug delivery applications

S. Dey, P. Sen, A. Patel, B. M. Prusty, S. S. Ghosh and D. Manna, Org. Biomol. Chem., 2022, 20, 7803 DOI: 10.1039/D2OB01332K

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