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Non-Viral Gene Delivery Vectors

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Cover of 'Non-Viral Gene Delivery Vectors'

Table of Contents

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    Book Overview
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    Chapter 1 Physical Chemical and Biomolecular Methods for the Optimization of Cationic Lipid-Based Lipoplexes In Vitro for the Gene Therapy Applications
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    Chapter 2 Non-Viral Gene Delivery Vectors
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    Chapter 3 Lipoplexes from Non-viral Cationic Vectors: DOTAP-DOPE Liposomes and Gemini Micelles
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    Chapter 4 Anionic/Zwitterionic Lipid-Based Gene Vectors of pDNA
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    Chapter 5 Elaboration and Physicochemical Characterization of Niosome-Based Nioplexes for Gene Delivery Purposes
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    Chapter 6 Quantitative Intracellular Localization of Cationic Lipid–Nucleic Acid Nanoparticles with Fluorescence Microscopy
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    Chapter 7 Targeted Delivery of Peptide-Tagged DNA Lipoplexes to Hepatocellular Carcinoma Cells
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    Chapter 8 Lipoplexes Strengthened by Anionic Polymers: Easy Preparation of Highly Effective siRNA Vectors Based on Cationic Lipids and Anionic Polymers
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    Chapter 9 Polymer Based Gene Silencing: In Vitro Delivery of SiRNA
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    Chapter 10 Polyallylamine Derivatives: Novel NonToxic Transfection Agents
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    Chapter 11 Biodegradable Three-Layered Micelles and Injectable Hydrogels
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    Chapter 12 Non-Viral Gene Delivery Vectors
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    Chapter 13 Non-Viral Gene Delivery Vectors
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    Chapter 14 Characterization and Investigation of Redox-Sensitive Liposomes for Gene Delivery
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    Chapter 15 From Artificial Amino Acids to Sequence-Defined Targeted Oligoaminoamides
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    Chapter 16 Gene Delivery Method Using Photo-Responsive Poly(β-Amino Ester) as Vectors
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    Chapter 17 Thermo-Responsive Polyplex Micelles with PEG Shells and PNIPAM Layer to Protect DNA Cores for Systemic Gene Therapy
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    Chapter 18 Application of Polyethylenimine-Grafted Silicon Nanowire Arrays for Gene Transfection
Attention for Chapter 9: Polymer Based Gene Silencing: In Vitro Delivery of SiRNA
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Chapter title
Polymer Based Gene Silencing: In Vitro Delivery of SiRNA
Chapter number 9
Book title
Non-Viral Gene Delivery Vectors
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3718-9_9
Pubmed ID
Book ISBNs
978-1-4939-3716-5, 978-1-4939-3718-9
Authors

Margarida I. Simão Carlos, Andreas Schätzlein, Ijeoma Uchegbu

Abstract

Gene silencing may be achieved by harnessing the RNA interference mechanism to effect down-regulation of protein expression. The therapeutic use of siRNA is dependent on its delivery to the intracellular space. This chapter describes the delivery of siRNA by N-(2-ethylamino)-6-O-glycolchitosan (EAGC). EAGC is a chitosan-based polymer, which binds to siRNA to form nanoparticles (NPs). The steps necessary to determine the delivery capacity of a polymer are presented in this chapter using EAGC as an example. The steps include: the transfection of cells with EAGC-siRNA polyplexes and protein detection by a Western Blotting assay.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 33%
Other 2 33%
Unknown 2 33%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 2 33%
Agricultural and Biological Sciences 1 17%
Engineering 1 17%
Unknown 2 33%