Evidence map›Paper›PMID 25437915›Full record

ArticleMolecular pharmaceutics2015

Screening nylon-3 polymers, a new class of cationic amphiphiles, for siRNA delivery.

Venkatareddy Nadithe, Runhui Liu, Bryan A Killinger, Sara Movassaghian, Na Hyung Kim, Anna B Moszczynska, Kristyn S Masters, Samuel H Gellman, Olivia M Merkel

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Beyond nylon 6: polyamidesChemical Society reviews · 2022
    Review
  4. Can pulmonary RNA delivery improve our pandemic preparedness?Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Venkatareddy NaditheDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University , Detroit, Michigan 48201, United States.
Runhui Liu
Bryan A Killinger
Sara Movassaghian
Na Hyung Kim
Anna B Moszczynska
Kristyn S Masters
Samuel H Gellman
Olivia M Merkel

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
Design and Analysis of Random Copolymers with Antimicrobial ActivityR01GM093265 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI WEISSHAAR, JAMES C. · 2011 to 2018
$2.1M
PROTEASOME AND PARKIN AS DRUG TARGETS AGAINST METHAMPHETAMINE TOXICITYR01DA034783 · NIDA · WAYNE STATE UNIVERSITY · PI MOSZCZYNSKA, ANNA · 2013 to 2017
$1.7M
Nylon-3 Copolymers as Synthetic Cell-Adhesive Moieties for Tissue EngineeringR21EB013259 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI GELLMAN, SAMUEL H., MASTERS, KRISTYN S · 2011 to 2012
$393k
NCI NIH HHS P30 CA022453NIBIB NIH HHS R21 EB013259NIBIB NIH HHS R21EB013259NIDA NIH HHS R01 DA034783NIGMS NIH HHS R01 GM093265NIGMS NIH HHS R01GM093265
6 · The paper itself

Abstract

Amphiphilic nucleic acid carriers have attracted strong interest. Three groups of nylon-3 copolymers (poly-β-peptides) possessing different cationic/hydrophobic content were evaluated as siRNA delivery agents in this study. Their ability to condense siRNA was determined in SYBR Gold assays. Their cytotoxicity was tested by MTT assays, their efficiency of delivering Alexa Fluor-488-labeled siRNA intracellularly in the presence and absence of uptake inhibitors was assessed by flow cytometry, and their transfection efficacies were studied by luciferase knockdown in a cell line stably expressing luciferase (H1299/Luc). Endosomal release was determined by confocal laser scanning microscopy and colocalization with lysotracker. All polymers efficiently condensed siRNA at nitrogen-to-phosphate (N/P) ratios of 5 or lower, as reflected in hydrodynamic diameters smaller than that at N/P 1. Although several formulations had negative zeta potentials at N/P 1, G2C and G2D polyplexes yielded >80% uptake in H1299/Luc cells, as determined by flow cytometry. Luciferase knockdown (20-65%) was observed after transfection with polyplexes made of the high molecular weight polymers that were the most hydrophobic. The ability of nylon-3 polymers to deliver siRNA intracellularly even at negative zeta potential implies that they mediate transport across cell membranes based on their amphiphilicity. The cellular uptake route was determined to strongly depend on the presence of cholesterol in the cell membrane. These polymers are, therefore, very promising for siRNA delivery at reduced surface charge and toxicity. Our study identified nylon-3 formulations at low N/P ratios for effective gene knockdown, indicating that nylon-3 polymers are a new, promising type of gene delivery agent.

Indexed as

Gene Transfer TechniquesCationsMolecular StructureNylonsPolymersRNA, Small InterferingTransfectionCationsNylonsPolymersRNA, Small Interferingnylon-3polyplexesRNAisiRNAtransfection

Identifiers

PMID25437915
PMCPMC4319696

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.