Evidence map›Paper›PMID 33809700›Full record

ArticlePharmaceutics2021

In-Vitro Application of Magnetic Hybrid Niosomes: Targeted siRNA-Delivery for Enhanced Breast Cancer Therapy.

Viktor Maurer, Selin Altin, Didem Ag Seleci, Ajmal Zarinwall, Bilal Temel, Peter M Vogt, Sarah Strauß, Frank Stahl, Thomas Scheper, Vesna Bucan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.9field-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

21 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
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  9. Article
  10. siRNA and targeted delivery systems in breast cancer therapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
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  12. Article
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  19. Lipid-Based Nanovesicular Drug Delivery Systems.Nanomaterials (Basel, Switzerland) · 2021
    Review
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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

11 authors at 3 institutions in 1 country.

Viktor MaurerInstitute for Particle Technology, Technische Universität Braunschweig, 38104 Braunschweig, Germany.
Selin AltinInstitute for Particle Technology, Technische Universität Braunschweig, 38104 Braunschweig, Germany.
Didem Ag SeleciInstitute for Particle Technology, Technische Universität Braunschweig, 38104 Braunschweig, Germany.
Ajmal ZarinwallInstitute for Particle Technology, Technische Universität Braunschweig, 38104 Braunschweig, Germany.
Bilal TemelInstitute for Particle Technology, Technische Universität Braunschweig, 38104 Braunschweig, Germany.
Peter M VogtDepartment of Plastic, Aesthetic, Hand and Reconstructive Surgery, Hannover Medical School, 30625 Hannover, Germany.
Sarah StraußDepartment of Plastic, Aesthetic, Hand and Reconstructive Surgery, Hannover Medical School, 30625 Hannover, Germany.
Frank StahlInstitute for Technical Chemistry, Leibniz University Hannover, 30167 Hannover, Germany.
Thomas ScheperInstitute for Technical Chemistry, Leibniz University Hannover, 30167 Hannover, Germany.
Vesna BucanDepartment of Plastic, Aesthetic, Hand and Reconstructive Surgery, Hannover Medical School, 30625 Hannover, Germany.
Georg GarnweitnerInstitute for Particle Technology, Technische Universität Braunschweig, 38104 Braunschweig, Germany.ORCID 0000-0002-7499-4947
Technische Universität Braunschweig · DEMedizinische Hochschule Hannover · DELeibniz University Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Even though the administration of chemotherapeutic agents such as erlotinib is clinically established for the treatment of breast cancer, its efficiency and the therapy outcome can be greatly improved using RNA interference (RNAi) mechanisms for a combinational therapy. However, the cellular uptake of bare small interfering RNA (siRNA) is insufficient and its fast degradation in the bloodstream leads to a lacking delivery and no suitable accumulation of siRNA inside the target tissues. To address these problems, non-ionic surfactant vesicles (niosomes) were used as a nanocarrier platform to encapsulate Lifeguard (LFG)-specific siRNA inside the hydrophilic core. A preceding entrapment of superparamagnetic iron-oxide nanoparticles (Fe

Indexed as

gene deliveryhybrid nanoparticlesmagnetic targetingniosomessiRNA

Identifiers

PMID33809700
PMCPMC8002368
OpenAlexW3138771523

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.