Issue 22, 2017

Surface-engineered mesoporous silica particles with luminescent, cytocompatible and targeting properties for cancer cell imaging

Abstract

To develop a novel cancer cell imaging approach, we fabricated surface-engineered mesoporous silica (MPS) particles with multi-functionalities. Specifically, mechanochemically-treated europium(III)-doped MPS (Eu:MPS) particles were prepared, and a folate N-hydroxysuccinimidyl ester (FA-NHS) molecule was immobilized on the particle surface as a targeting ligand for specific types of cells. With the mechanochemical treatment, the siloxane bonds were changed to show better luminescence quantum efficiency as revealed by 29Si-NMR and photoluminescence spectroscopy, suggesting interaction changes between the silica framework structures and the doped Eu ions. Furthermore, the mechanochemically-treated particles immobilized with FA-NHS specifically bind to the cancer cells and the subsequent uptake by the cells was in situ observed using time-lapse optical microscopy. The particles did not exhibit any toxicity in the cellular proliferation stages. The particles after the binding and uptake also showed intense luminescence from the cells at a culture time of 24 h, demonstrating a clear imaging ability along with all the cellular shapes. Therefore, the present surface-engineered luminescent particles will be used for specific cancer targeting and imaging purposes.

Graphical abstract: Surface-engineered mesoporous silica particles with luminescent, cytocompatible and targeting properties for cancer cell imaging

Supplementary files

Article information

Article type
Paper
Submitted
13 Jan 2017
Accepted
23 Feb 2017
First published
01 Mar 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 13643-13652

Surface-engineered mesoporous silica particles with luminescent, cytocompatible and targeting properties for cancer cell imaging

M. Tagaya, S. Abe, S. Motozuka, K. Shiba, T. Takemura, I. Hayashi and Y. Sakaguchi, RSC Adv., 2017, 7, 13643 DOI: 10.1039/C7RA00535K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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