Evidence map›Paper›PMID 26690119›Full record

ReviewInternational journal of molecular sciences2015

Cell Penetrating Peptide Conjugated Chitosan for Enhanced Delivery of Nucleic Acid.

Buddhadev Layek, Lindsey Lipp, Jagdish Singh

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
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

32 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Non-Invasive Intranasal Delivery ofInternational journal of molecular sciences · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Antifungal Carvacrol Loaded Chitosan Nanoparticles.Antibiotics (Basel, Switzerland) · 2021
    Article
  14. Cyclic Peptide-Gadolinium Nanocomplexes as siRNA Delivery Tools.Pharmaceuticals (Basel, Switzerland) · 2021
    Article
  15. Article
  16. A review of the tortuous path of nonviral gene delivery and recent progress.International journal of biological macromolecules · 2021
    Review
  17. Article
  18. Review
  19. Review
  20. MicroRNA delivery through nanoparticles.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Review
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

3 authors at 2 institutions in 1 country.

Buddhadev LayekDepartment of Pharmaceutics, College of Pharmacy, University of Minnesota, 308 Harvard Street S.E., Minneapolis, MN 55455, USA. blayek@umn.edu.
Lindsey LippDepartment of Pharmaceutical Sciences, School of Pharmacy, North Dakota State University, Fargo, ND 58105, USA. lindsey.will@ndsu.edu.
Jagdish SinghDepartment of Pharmaceutical Sciences, School of Pharmacy, North Dakota State University, Fargo, ND 58105, USA. jagdish.singh@ndsu.edu.
North Dakota State University · USUniversity of Minnesota · US

Funding

Modification of insulin molecule for controlled delivery at basal level from triblock copolymersR15GM114701 · NIGMS · NORTH DAKOTA STATE UNIVERSITY · PI SINGH, JAGDISH · 2015 to 2015
$348k
NIGMS NIH HHS R15 GM114701
6 · The paper itself

Abstract

Gene therapy is an emerging therapeutic strategy for the cure or treatment of a spectrum of genetic disorders. Nevertheless, advances in gene therapy are immensely reliant upon design of an efficient gene carrier that can deliver genetic cargoes into the desired cell populations. Among various nonviral gene delivery systems, chitosan-based carriers have gained increasing attention because of their high cationic charge density, excellent biocompatibility, nearly nonexistent cytotoxicity, negligible immune response, and ideal ability to undergo chemical conjugation. However, a major shortcoming of chitosan-based carriers is their poor cellular uptake, leading to inadequate transfection efficiency. The intrinsic feature of cell penetrating peptides (CPPs) for transporting diverse cargoes into multiple cell and tissue types in a safe manner suggests that they can be conjugated to chitosan for improving its transfection efficiency. In this review, we briefly discuss CPPs and their classification, and also the major mechanisms contributing to the cellular uptake of CPPs and cargo conjugates. We also discuss immense improvements for the delivery of nucleic acids using CPP-conjugated chitosan-based carriers with special emphasis on plasmid DNA and small interfering RNA.

Indexed as

Gene Transfer TechniquesAnimalsCell-Penetrating PeptidesChitosanEndocytosisHumansModels, MolecularNucleic AcidsPlasmidsRNA, Small InterferingCell-Penetrating PeptidesChitosanNucleic AcidsRNA, Small Interferingcell penetrating peptides (CPPs)cellular uptakechitosangene deliverynonviral vectortransfection

Identifiers

PMID26690119
PMCPMC4691089
OpenAlexW2186118124

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.