Evidence map›Paper›PMID 24658111›Full record

ArticlePloS one2014

Microfluidic-enabled liposomes elucidate size-dependent transdermal transport.

Renee R Hood, Eric L Kendall, Mariana Junqueira, Wyatt N Vreeland, Zenaide Quezado, Julia C Finkel, Don L DeVoe

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Hetero-Multivalent Targeted Liposomal Drug Delivery to TreatACS applied materials & interfaces · 2022
    Article
  9. Review
  10. Formulation ofDrug delivery and translational research · 2018
    Article
  11. 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

7 authors.

Renee R HoodFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States of America.
Eric L KendallDepartment of Mechanical Engineering, University of Maryland, College Park, Maryland, United States of America.
Mariana JunqueiraDepartment of Anesthesiology, Sedation, and Perioperative Medicine, Children's National Medical Center, Washington, DC, United States of America.
Wyatt N VreelandBiomolecular Measurement Division, National Institute of Standards and Technology, Gaithersburg, Maryland, United States of America.
Zenaide QuezadoDepartment of Anesthesiology, Sedation, and Perioperative Medicine, Children's National Medical Center, Washington, DC, United States of America.
Julia C FinkelDepartment of Anesthesiology, Sedation, and Perioperative Medicine, Children's National Medical Center, Washington, DC, United States of America.
Don L DeVoeFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States of America; Department of Mechanical Engineering, University of Maryland, College Park, Maryland, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microfluidic synthesis of small and nearly-monodisperse liposomes is used to investigate the size-dependent passive transdermal transport of nanoscale lipid vesicles. While large liposomes with diameters above 105 nm are found to be excluded from deeper skin layers past the stratum corneum, the primary barrier to nanoparticle transport, liposomes with mean diameters between 31-41 nm exhibit significantly enhanced penetration. Furthermore, multicolor fluorescence imaging reveals that the smaller liposomes pass rapidly through the stratum corneum without vesicle rupture. These findings reveal that nanoscale liposomes with well-controlled size and minimal size variance are excellent vehicles for transdermal delivery of functional nanoparticle drugs.

Indexed as

MicrofluidicsAdministration, CutaneousAnimalsBiological TransportDrug Delivery SystemsHydrophobic and Hydrophilic InteractionsLiposomesNanoparticlesParticle SizePermeabilityPolyethylene GlycolsSkinSkin AbsorptionSwineTime FactorsLiposomesPolyethylene Glycols

Identifiers

PMID24658111
PMCPMC3962493

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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.