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SiRNA Delivery Methods

Overview of attention for book
Cover of 'SiRNA Delivery Methods'

Table of Contents

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    Book Overview
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    Chapter 1 Synthesis and Conjugation of Small Interfering Ribonucleic Neutral SiRNNs.
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    Chapter 2 Liver-Targeted SiRNA Delivery Using Biodegradable Poly(amide) Polymer Conjugates
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    Chapter 3 SiRNA Delivery Methods
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    Chapter 4 Highly Efficient SiRNA Delivery Mediated by Cationic Helical Polypeptides and Polypeptide-Based Nanosystems
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    Chapter 5 Disulfide-Bridged Cleavable PEGylation of Poly- l -Lysine for SiRNA Delivery
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    Chapter 6 Preparation of a Cyclic RGD: Modified Liposomal SiRNA Formulation for Use in Active Targeting to Tumor and Tumor Endothelial Cells
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    Chapter 7 A Multifunctional Envelope-Type Nano Device Containing a pH-Sensitive Cationic Lipid for Efficient Delivery of Short Interfering RNA to Hepatocytes In Vivo
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    Chapter 8 Bioreducible Poly(Beta-Amino Ester)s for Intracellular Delivery of SiRNA
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    Chapter 9 Preparation of Polyion Complex Micelles Using Block Copolymers for SiRNA Delivery
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    Chapter 10 Delivery of Small Interfering RNAs to Cells via Exosomes.
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    Chapter 11 Dendrimer Nanovectors for SiRNA Delivery.
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    Chapter 12 Chitosan Nanoparticles for SiRNA Delivery In Vitro
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    Chapter 13 Non-Covalently Functionalized of Single-Walled Carbon Nanotubes by DSPE-PEG-PEI for SiRNA Delivery
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    Chapter 14 SiRNA In Vivo-Targeted Delivery to Murine Dendritic Cells by Oral Administration of Recombinant Yeast.
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    Chapter 15 TLR9-Targeted SiRNA Delivery In Vivo.
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    Chapter 16 Aptamer-MiRNA Conjugates for Cancer Cell-Targeted Delivery.
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    Chapter 17 Method for Confirming Cytoplasmic Delivery of RNA Aptamers.
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    Chapter 18 Hapten-Binding Bispecific Antibodies for the Targeted Delivery of SiRNA and SiRNA-Containing Nanoparticles
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    Chapter 19 Stable Delivery of CCR5-Directed shRNA into Human Primary Peripheral Blood Mononuclear Cells and Hematopoietic Stem/Progenitor Cells via a Lentiviral Vector.
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    Chapter 20 Hepatic Delivery of Artificial Micro RNAs Using Helper-Dependent Adenoviral Vectors.
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    Chapter 21 Intravascular AAV9 Administration for Delivering RNA Silencing Constructs to the CNS and Periphery.
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    Chapter 22 Efficient Gene Suppression in Dorsal Root Ganglia and Spinal Cord Using Adeno-Associated Virus Vectors Encoding Short-Hairpin RNA.
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    Chapter 23 Synthetic SiRNA Delivery: Progress and Prospects.
Attention for Chapter 17: Method for Confirming Cytoplasmic Delivery of RNA Aptamers.
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Chapter title
Method for Confirming Cytoplasmic Delivery of RNA Aptamers.
Chapter number 17
Book title
SiRNA Delivery Methods
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3112-5_17
Pubmed ID
Book ISBNs
978-1-4939-3111-8, 978-1-4939-3112-5
Authors

Dickey, David D, Thomas, Gregory S, Dassie, Justin P, Giangrande, Paloma H, David D. Dickey, Gregory S. Thomas, Justin P. Dassie, Paloma H. Giangrande, Dickey, David D., Thomas, Gregory S., Dassie, Justin P., Giangrande, Paloma H.

Abstract

RNA aptamers are single-stranded RNA oligos that represent a powerful emerging technology with potential for treating numerous diseases. More recently, cell-targeted RNA aptamers have been developed for delivering RNA interference (RNAi) modulators (siRNAs and miRNAs) to specific diseased cells (e.g., cancer cells or HIV infected cells) in vitro and in vivo. However, despite initial promising reports, the broad application of this aptamer delivery technology awaits the development of methods that can verify and confirm delivery of aptamers to the cytoplasm of target cells where the RNAi machinery resides. We recently developed a functional assay (RIP assay) to confirm cellular uptake and subsequent cytoplasmic release of an RNA aptamer which binds to a cell surface receptor expressed on prostate cancer cells (PSMA). To assess cytoplasmic delivery, the aptamer was chemically conjugated to saporin, a ribosome inactivating protein toxin that is toxic to cells only when delivered to the cytoplasm (where it inhibits the ribosome) by a cell-targeting ligand (e.g., aptamer). Here, we describe the chemistry used to conjugate the aptamer to saporin and discuss a gel-based method to verify conjugation efficiency. We also detail an in vitro functional assay to confirm that the aptamer retains function following conjugation to saporin and describe a cellular assay to measure aptamer-mediated saporin-induced cytotoxicity.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 21 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
China 1 5%
Unknown 20 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 38%
Student > Ph. D. Student 4 19%
Unspecified 2 10%
Other 1 5%
Student > Bachelor 1 5%
Other 2 10%
Unknown 3 14%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 24%
Agricultural and Biological Sciences 5 24%
Pharmacology, Toxicology and Pharmaceutical Science 2 10%
Unspecified 2 10%
Environmental Science 1 5%
Other 3 14%
Unknown 3 14%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 19 October 2015.
All research outputs
#13,449,421
of 22,830,751 outputs
Outputs from Methods in molecular biology
#3,620
of 13,126 outputs
Outputs of similar age
#189,574
of 393,540 outputs
Outputs of similar age from Methods in molecular biology
#349
of 1,470 outputs
Altmetric has tracked 22,830,751 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,126 research outputs from this source. They receive a mean Attention Score of 3.4. This one has gotten more attention than average, scoring higher than 70% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 393,540 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 50% of its contemporaries.
We're also able to compare this research output to 1,470 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 74% of its contemporaries.