Issue 118, 2015

One pot synthesis of doxorubicin loaded gold nanoparticles for sustained drug release

Abstract

Here, we report a facile, versatile and simple one-pot synthesis of doxorubicin (Dox) loaded gold nanoparticles (Dox–GNP conjugate), where Dox can act both as a reducing as well as a capping agent. Interestingly, when the conjugate was placed into the transporter protein environment, it avoided the undesirable multilayer protein corona formation, which is very common for nanomaterials. The in vitro drug release kinetic studies and the cytotoxicity assay and cellular update efficiency advocates that the system is capable of sustained release of the drug even in the presence of a complex biological environment.

Graphical abstract: One pot synthesis of doxorubicin loaded gold nanoparticles for sustained drug release

Supplementary files

Article information

Article type
Communication
Submitted
02 Jul 2015
Accepted
04 Nov 2015
First published
09 Nov 2015

RSC Adv., 2015,5, 97330-97334

Author version available

One pot synthesis of doxorubicin loaded gold nanoparticles for sustained drug release

A. Chaudhary, C. Dwivedi, A. Gupta and C. K. Nandi, RSC Adv., 2015, 5, 97330 DOI: 10.1039/C5RA12892G

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