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Biomedical Nanotechnology

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Cover of 'Biomedical Nanotechnology'

Table of Contents

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    Book Overview
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    Chapter 1 Quantification of siRNA Duplexes Bound to Gold Nanoparticle Surfaces
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    Chapter 2 Ligand Exchange and 1H NMR Quantification of Single- and Mixed-Moiety Thiolated Ligand Shells on Gold Nanoparticles
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    Chapter 3 Nanoparticle Tracking Analysis for Determination of Hydrodynamic Diameter, Concentration, and Zeta-Potential of Polyplex Nanoparticles
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    Chapter 4 Magnetic Characterization of Iron Oxide Nanoparticles for Biomedical Applications
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    Chapter 5 Preparation of Magnetic Nanoparticles for Biomedical Applications
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    Chapter 6 Brain-Penetrating Nanoparticles for Analysis of the Brain Microenvironment
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    Chapter 7 Volumetric Bar-Chart Chips for Biosensing
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    Chapter 8 qFlow Cytometry-Based Receptoromic Screening: A High-Throughput Quantification Approach Informing Biomarker Selection and Nanosensor Development
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    Chapter 9 Evaluating Nanoparticle Binding to Blood Compartment Immune Cells in High-Throughput with Flow Cytometry
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    Chapter 10 A Gold@Polydopamine Core–Shell Nanoprobe for Long-Term Intracellular Detection of MicroRNAs in Differentiating Stem Cells
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    Chapter 11 Antibody-Conjugated Single Quantum Dot Tracking of Membrane Neurotransmitter Transporters in Primary Neuronal Cultures
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    Chapter 12 Spectroscopic Photoacoustic Imaging of Gold Nanorods
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    Chapter 13 Dual Wavelength-Triggered Gold Nanorods for Anticancer Treatment
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    Chapter 14 Photolabile Self-Immolative DNA-Drug Nanostructures
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    Chapter 15 Enzyme-Responsive Nanoparticles for the Treatment of Disease
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    Chapter 16 NanoScript: A Versatile Nanoparticle-Based Synthetic Transcription Factor for Innovative Gene Manipulation
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    Chapter 17 Glucose-Responsive Insulin Delivery by Microneedle-Array Patches Loaded with Hypoxia-Sensitive Vesicles
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    Chapter 18 Electrospun Nanofiber Scaffolds and Their Hydrogel Composites for the Engineering and Regeneration of Soft Tissues
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    Chapter 19 Application of Hydrogel Template Strategy in Ocular Drug Delivery
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    Chapter 20 High-Accuracy Determination of Cytotoxic Responses from Graphene Oxide Exposure Using Imaging Flow Cytometry
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    Chapter 21 Air–Liquid Interface Cell Exposures to Nanoparticle Aerosols
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    Chapter 22 Returning to the Patent Landscapes for Nanotechnology: Assessing the Garden that It Has Grown Into
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    Chapter 23 Erratum to: Biomedical Nanotechnology
Attention for Chapter 20: High-Accuracy Determination of Cytotoxic Responses from Graphene Oxide Exposure Using Imaging Flow Cytometry
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Chapter title
High-Accuracy Determination of Cytotoxic Responses from Graphene Oxide Exposure Using Imaging Flow Cytometry
Chapter number 20
Book title
Biomedical Nanotechnology
Published in
Methods in molecular biology, February 2017
DOI 10.1007/978-1-4939-6840-4_20
Pubmed ID
Book ISBNs
978-1-4939-6838-1, 978-1-4939-6840-4
Authors

Sandra Vranic, Kostas Kostarelos

Editors

Sarah Hurst Petrosko, Emily S. Day

Abstract

Graphene and other 2D materials have received increased attention in the biomedical field due to their unique properties and potential use as carriers for targeted drug delivery or in regenerative medicine. Before the exploitation of graphene-based materials in biomedicine becomes a reality, it is necessary to establish the full toxicological profile and better understand how the material interacts with cells and tissues. Because specific properties, such as flake size and surface chemistry, might determine whether graphene can achieve therapeutic efficacy without causing toxicity, it is important to develop highly accurate and reliable screening techniques to accurately assess the biocompatibility of different types of graphene-based materials. In this protocol, we describe a method to achieve accurate determination of the cytotoxic response following in vitro exposure to large graphene oxide (L-GO) sheets using annexin V/propidium iodide staining and the Imagestream(®) platform. The proposed protocol is especially suitable for the toxicity assessment of carbonaceous materials that form aggregates in cell culture media, which is a common occurrence. We describe how to best gate out any interfering signals coming from the material by visual inspection and by using powerful software, thus performing the analysis of cellular death on a selected population of cells with higher accuracy and statistical relevance compared to conventional flow cytometry.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 9 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 44%
Professor > Associate Professor 1 11%
Unknown 4 44%
Readers by discipline Count As %
Veterinary Science and Veterinary Medicine 1 11%
Biochemistry, Genetics and Molecular Biology 1 11%
Physics and Astronomy 1 11%
Medicine and Dentistry 1 11%
Unknown 5 56%