| Literature DB >> 30608496 |
Zeid A Nima1, Kieng Bao Vang1, Dmitry Nedosekin2, Ganesh Kannarpady1, Viney Saini1, Shawn E Bourdo1, Waqar Majeed1, Fumiya Watanabe1, Emilie Darrigues1, Karrer M Alghazali1, Raad A Alawajji1, Dayton Petibone3, Syed Ali4, Alexandru R Biris5, Daniel Casciano1, Anindya Ghosh1, Gregory Salamo6, Vladimir Zharov2, Alexandru S Biris1.
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.Entities:
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Year: 2019 PMID: 30608496 PMCID: PMC9261879 DOI: 10.1039/c8nr06847j
Source DB: PubMed Journal: Nanoscale ISSN: 2040-3364 Impact factor: 8.307