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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 13: Dual Wavelength-Triggered Gold Nanorods for Anticancer Treatment
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Chapter title
Dual Wavelength-Triggered Gold Nanorods for Anticancer Treatment
Chapter number 13
Book title
Biomedical Nanotechnology
Published in
Methods in molecular biology, February 2017
DOI 10.1007/978-1-4939-6840-4_13
Pubmed ID
Book ISBNs
978-1-4939-6838-1, 978-1-4939-6840-4
Authors

Dennis B. Pacardo, Frances S. Ligler, Zhen Gu, Pacardo, Dennis B., Ligler, Frances S., Gu, Zhen

Editors

Sarah Hurst Petrosko, Emily S. Day

Abstract

Gold nanomaterials with light-responsive properties can be exploited as light-triggered delivery vehicles to enhance the therapeutic efficacy of anticancer drugs. Additionally, different wavelengths of light can be utilized to achieve the combined effects of light-triggered release of therapeutics and light-induced localized heating, which results in improved anticancer efficacy. Herein, we describe methods to develop gold nanorod (AuNR) complexes that provide drug delivery or photothermal therapy when activated by ultraviolet (UV) or near-infrared (NIR) wavelengths of light, respectively. The surface functionalization of AuNRs with three key components is presented. The first component, cyclodextrin, serves to encapsulate drugs of interest. The second component, dextran-phenyl-azo-benzoic acid (DexAzo), serves as a capping agent that undergoes a conformational change upon UV light activation to expose the drugs for release. The third component is a folic acid-based targeting ligand that provides efficient delivery of the AuNR complexes to cancer cells. The dual wavelength activation of these drug-loaded AuNR complexes, which enables one to achieve highly efficient anticancer therapy through the combined effects of UV-triggered drug release and NIR-induced hyperthermia, is also described.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 25%
Researcher 1 25%
Unknown 2 50%
Readers by discipline Count As %
Materials Science 1 25%
Medicine and Dentistry 1 25%
Unknown 2 50%