Evidence map›Paper›PMID 29141461›Full record

ArticleDrug delivery2017

Development of magnetic anionic liposome/atelocollagen complexes for efficient magnetic drug targeting.

Yusuke Kono, Taketo Nakai, Hitomi Taguchi, Takuya Fujita

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Current research trends of nanomedicines.Acta pharmaceutica Sinica. B · 2023
    Review
  3. Article
  4. Article
  5. Review
  6. 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

4 authors at 1 institution in 1 country.

Yusuke Konoa Laboratory of Molecular Pharmacokinetics, College of Pharmaceutical Sciences , Ritsumeikan University , Kusatsu , Japan.
Taketo Nakaia Laboratory of Molecular Pharmacokinetics, College of Pharmaceutical Sciences , Ritsumeikan University , Kusatsu , Japan.
Hitomi Taguchia Laboratory of Molecular Pharmacokinetics, College of Pharmaceutical Sciences , Ritsumeikan University , Kusatsu , Japan.
Takuya Fujitaa Laboratory of Molecular Pharmacokinetics, College of Pharmaceutical Sciences , Ritsumeikan University , Kusatsu , Japan.
Ritsumeikan University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Magnetic nanoparticle-incorporated liposomes (magnetic liposomes) are considered a promising site-specific drug delivery carrier vehicle. With regard to their surface charge, magnetic anionic liposomes (Mag-AL) demonstrate little toxicity in comparison with magnetic cationic liposomes (Mag-CL), whereas their cellular association and uptake efficiency are low. In the current study, we constructed complexes of Mag-AL and atelocollagen (ATCOL), which is a biocompatible and minimally immunogenic biomaterial, to improve the cellular uptake properties of Mag-AL in vitro and in vivo. The cellular association and/or uptake of Mag-AL in RAW264 cells, a murine macrophage-like cell line, under a magnetic field was significantly increased when Mag-AL was complexed with ATCOL, and the highest cellular association was observed with complexes constructed using 5 µg/mL of ATCOL. The complexes showed liposome concentration-dependent and time-dependent cellular association under a magnetic field, and their cellular uptake efficiency was comparable with that of Mag-CL. In addition, Mag-CL showed significant cytotoxicity in a liposome concentration-dependent manner, whereas Mag-AL/ATCOL complexes produced no cytotoxic effect against RAW264 cells. Furthermore, the efficient cellular association of Mag-AL/ATCOL complexes in RAW264 cells was observed even in the presence of serum, and their liver accumulation was significantly increased at a magnetic field-exposed region after intravenous injection in rats. These results indicate that Mag-AL/ATCOL complexes could be a safe and efficient magnetic responsive drug carrier.

Indexed as

AnimalsAnionsBiocompatible MaterialsCell LineCell Line, TumorCollagenDrug CarriersDrug Delivery SystemsLiposomesLiverMagneticsMaleMiceRatsRats, Sprague-DawleyRAW 264.7 CellsAnionsatelocollagenBiocompatible MaterialsCollagenDrug CarriersLiposomesanionic liposomesatelocollagencationic liposomesMagnetic drug targetingmagnetic field

Identifiers

PMID29141461
PMCPMC8241088
OpenAlexW2769766790

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.