Evidence map›Paper›PMID 31546717›Full record

ArticleInternational journal of molecular sciences2019

Rapid Microfluidic Preparation of Niosomes for Targeted Drug Delivery.

Didem Ag Seleci, Viktor Maurer, Frank Stahl, Thomas Scheper, Georg Garnweitner

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Nanoparticle Carriers: A New Era of Precise CRISPR/Cas9 Gene Editing.MicroRNA (Shariqah, United Arab Emirates) · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Niosomes: a novel targeted drug delivery system for cancer.Medical oncology (Northwood, London, England) · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Fabrication and Applications of Microfluidic Devices: A Review.International journal of molecular sciences · 2021
    Review
  20. 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

5 authors.

Didem Ag SeleciInstitute for Particle Technology (iPAT), Technische Universität Braunschweig, 38104 Braunschweig, Germany. d.ag-seleci@tu-braunschweig.de.
Viktor MaurerInstitute for Particle Technology (iPAT), Technische Universität Braunschweig, 38104 Braunschweig, Germany. v.maurer@tu-braunschweig.de.
Frank StahlInstitute for Technical Chemistry, Leibniz University Hannover, 30167 Hannover, Germany. stahl@iftc.uni-hannover.de.
Thomas ScheperInstitute for Technical Chemistry, Leibniz University Hannover, 30167 Hannover, Germany. scheper@iftc.uni-hannover.de.
Georg GarnweitnerInstitute for Particle Technology (iPAT), Technische Universität Braunschweig, 38104 Braunschweig, Germany. g.garnweitner@tu-braunschweig.de.ORCID 0000-0002-7499-4947

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Niosomes are non-ionic surfactant-based vesicles with high promise for drug delivery applications. They can be rapidly prepared via microfluidics, allowing their reproducible production without the need of a subsequent size reduction step, by controlled mixing of two miscible phases of an organic (lipids dissolved in alcohol) and an aqueous solution in a microchannel. The control of niosome properties and the implementation of more complex functions, however, thus far are largely unknown for this method. Here we investigate microfluidics-based manufacturing of topotecan (TPT)-loaded polyethylene glycolated niosomes (PEGNIO). The flow rate ratio of the organic and aqueous phases was varied and optimized. Furthermore, the surface of TPT-loaded PEGNIO was modified with a tumor homing and penetrating peptide (tLyp-1). The designed nanoparticular drug delivery system composed of PEGNIO-TPT-tLyp-1 was fabricated for the first time via microfluidics in this study. The physicochemical properties were determined through dynamic light scattering (DLS) and zeta potential analysis. In vitro studies of the obtained formulations were performed on human glioblastoma (U87) cells. The results clearly indicated that tLyp-1-functionalized TPT-loaded niosomes could significantly improve anti-glioma treatment.

Indexed as

Drug Delivery SystemsLiposomesMicrofluidicsCell Line, TumorDrug CarriersDrug CompoundingDrug LiberationHumansParticle SizeDrug CarriersLiposomesgliomamicrofluidicsniosomestargeted drug delivery

Identifiers

PMID31546717
PMCPMC6801367

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.