Issue 12, 2016

Intelligent Janus nanoparticles for intracellular real-time monitoring of dual drug release

Abstract

Stimuli-responsive nanomaterials have been receiving much attention as drug delivery carriers, however understanding of multi-drug release from the carriers for efficient therapeutics is highly challenging. Here, we report a novel nanosystem, Janus particle Dox-CMR-MS/Au-6MP (Dox: doxorubicin, CMR: 7-hydroxycoumarin-3-carboxylate, MS: mesoporous silica, Au: gold, 6MP: 6-mercaptopurine) with opposing MS and Au faces, which can monitor intracellular dual-drug (Dox and 6MP) controlled release in real time based on fluorescence resonance energy transfer (FRET) and surface-enhanced Raman scattering (SERS). The FRET acceptor Dox is attached to CMR (as a FRET donor) conjugated MS with a pH-responsive linker hydrazone, and 6MP is conjugated to the Au surface through the gold–thiol interaction. As the Janus nanoparticle enters into tumor cells, the breakage of the hydrazone bond in an acidic environment and the substitution of glutathione (GSH) overexpressed in cancer cells give rise to the release of Dox and 6MP, respectively. Thus, the change of the CMR fluorescence signal and the SERS decrease of 6MP can be used to monitor the dual-drug release within living cells in real time. In addition, this work demonstrates the enhanced anticancer effect of the designed dual-drug loaded nanosystem. Therefore, the current study may provide new perspectives for the real-time study of intelligent multi-drug delivery and release, as well as cellular responses to drug treatment.

Graphical abstract: Intelligent Janus nanoparticles for intracellular real-time monitoring of dual drug release

Supplementary files

Article information

Article type
Paper
Submitted
03 Feb 2016
Accepted
11 Feb 2016
First published
17 Feb 2016

Nanoscale, 2016,8, 6754-6760

Author version available

Intelligent Janus nanoparticles for intracellular real-time monitoring of dual drug release

H. Cao, Y. Yang, X. Chen and Z. Shao, Nanoscale, 2016, 8, 6754 DOI: 10.1039/C6NR00987E

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