Issue 44, 2021

Ethidium bromide-bridged mesoporous silica hybrid nanocarriers for fluorescence cell imaging and drug delivery applications

Abstract

Mesoporous silica nanocarriers with dual/multifunctionalities are thought to be good candidates for dual/multimodal applications such as combined drug delivery and bioimaging. In this study, new red fluorescent organosilica materials were conveniently produced with diurea-ethidium bromide (DU-EB) functional units integrated in the pore wall framework for simultaneous diagnosis and therapy. We found that the prepared mesoporous silica hybrid nanocarrier system exhibited strong red fluorescence under UV-light (365 nm) while retaining excellent photo- and chemical-stability. The integrated ethidium bromide functional units in the mesopore walls cause the red fluorescence. By loading/releasing doxorubicin (Dox)/5-fluorouracil (5-FU) as a model cargo, the synthesized DU-EB@MSH materials were tested at various pH levels (pH 5.0, 6.2 and 7.4), and the cytocompatibility of the red-fluorescent DU-EB@MSH nanocarrier system was assessed using human breast cancer (MCF-7) cells. The experimental results revealed that the drug release behavior is primarily determined by the pH of the intracellular medium, and red-fluorescence was induced by a UV-light (365 nm) trigger. All the study results suggested that the DU-EB@MSH drug carrier system could be useful for red-fluorescence bioimaging and chemotherapeutic applications in cancer therapy.

Graphical abstract: Ethidium bromide-bridged mesoporous silica hybrid nanocarriers for fluorescence cell imaging and drug delivery applications

Supplementary files

Article information

Article type
Paper
Submitted
22 Jul 2021
Accepted
10 Sep 2021
First published
05 Oct 2021

New J. Chem., 2021,45, 20641-20648

Ethidium bromide-bridged mesoporous silica hybrid nanocarriers for fluorescence cell imaging and drug delivery applications

M. Santhamoorthy, K. Thirupathi, T. Periyasamy, D. Thirumalai, V. Ramkumar and S. Kim, New J. Chem., 2021, 45, 20641 DOI: 10.1039/D1NJ03520G

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