Issue 3, 2019

Quantification of cellular associated graphene and induced surface receptor responses

Abstract

The use of graphene for biomedical and other applications involving humans is growing and shows practical promise. However, quantifying the graphitic nanomaterials that interact with cells and assessing any corresponding cellular response is extremely challenging. Here, we report an effective approach to quantify graphene interacting with single cells that utilizes combined multimodal-Raman and photoacoustic spectroscopy. This approach correlates the spectroscopic signature of graphene with the measurement of its mass using a quartz crystal microbalance resonator. Using this technique, we demonstrate single cell noninvasive quantification and multidimensional mapping of graphene with a detection limit of as low as 200 femtograms. Our investigation also revealed previously unseen graphene-induced changes in surface receptor expression in dendritic cells of the immune system. This tool integrates high-sensitivity real-time detection and monitoring of nanoscale materials inside single cells with the measurement of induced simultaneous biological cell responses, providing a powerful method to study the impact of nanomaterials on living systems and as a result, the toxicology of nanoscale materials.

Graphical abstract: Quantification of cellular associated graphene and induced surface receptor responses

Supplementary files

Article information

Article type
Paper
Submitted
23 Aug 2018
Accepted
10 Dec 2018
First published
04 Jan 2019

Nanoscale, 2019,11, 932-944

Author version available

Quantification of cellular associated graphene and induced surface receptor responses

Z. A. Nima, K. B. Vang, D. Nedosekin, G. Kannarpady, V. Saini, S. E. Bourdo, W. Majeed, F. Watanabe, E. Darrigues, K. M. Alghazali, R. A. Alawajji, D. Petibone, S. Ali, A. R. Biris, D. Casciano, A. Ghosh, G. Salamo, V. Zharov and A. S. Biris, Nanoscale, 2019, 11, 932 DOI: 10.1039/C8NR06847J

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