Evidence map›Paper›PMID 29045127›Full record

ArticleACS nano2017

Revealing Dynamics of Accumulation of Systemically Injected Liposomes in the Skin by Intravital Microscopy.

James I Griffin, Guankui Wang, Weston J Smith, Vivian P Vu, Robert Scheinman, Dominik Stitch, Radu Moldovan, Seyed Moein Moghimi, Dmitri Simberg

Abstract read
In one paragraph

Article in ACS nano, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Engineering of Cell Derived-Nanovesicle as an Alternative to Exosome Therapy.Tissue engineering and regenerative medicine · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Delivery of a model lipophilic membrane cargo to bone marrow via cell-derived microparticles.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
  10. A framework for designing delivery systems.Nature nanotechnology · 2020
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Adapting liposomes for oral drug delivery.Acta pharmaceutica Sinica. B · 2019
    Review
  16. Review
  17. Nanoparticle transport pathways into tumors.Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology · 2018
    Article
  18. Histological findings for the absorption of small and large liposomes - the basis of future drug delivery and contrast media systems.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
  19. 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

9 authors at 2 institutions in 2 countries.

James I Griffin
Guankui Wang
Weston J Smith
Vivian P Vu
Robert Scheinman
Dominik StitchAdvanced Light Microscopy Core Facility, University of Colorado Anschutz Medical Campus , Aurora, Colorado 80045, United States.
Radu MoldovanAdvanced Light Microscopy Core Facility, University of Colorado Anschutz Medical Campus , Aurora, Colorado 80045, United States.
Seyed Moein MoghimiSchool of Pharmacy, The Faculty of Medical Sciences, Newcastle University , King George VI Building, Newcastle upon Tyne NE1 7RU, U.K.ORCID 0000-0003-0836-926X
University of Colorado Anschutz Medical Campus · USNewcastle University · GB

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
Painted erythrocyte carriers for therapy of acute myeloid leukemiaR01CA194058 · NCI · UNIVERSITY OF COLORADO DENVER · PI SIMBERG, DMITRI · 2016 to 2020
$1.8M
The alternative complement pathway and hemocompatibility of nanosurfacesR01EB022040 · NIBIB · UNIVERSITY OF COLORADO DENVER · PI SIMBERG, DMITRI · 2016 to 2019
$1.4M
NCATS NIH HHS UL1 TR001082NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA194058NIBIB NIH HHS R01 EB022040NINDS NIH HHS P30 NS048154
6 · The paper itself

Abstract

Accumulation of intravenously injected cytotoxic liposomes in the skin induces serious toxicity. We used single time point and longitudinal intravital microscopy to understand skin accumulation dynamics of non-PEGylated and PEGylated liposomes after systemic injection into mice. Non-PEGylated egg phosphatidylcholine (PC) liposomes showed short circulation half-life (1.3 h) and immediate aggregation in the blood, with some aggregates lodging in skin microvasculature soon after the injection. At 24 h, and more prominently at 48 h postinjection, liposomes appeared in dermal and subdermal cells. PEGylated egg PC liposomes showed long circulation half-life (22 h) and no aggregation in the blood. PEGylated liposomes started to accumulate in the skin microvasculature as soon as 5 min after the injection. Within 3 h postinjection, PEGylated liposomes accumulated in extravascular cells in the dermis and subdermis. Liposomes were present in the skin for at least 7 days postinjection. A regulatory approved PEGylated liposomal doxorubicin (LipoDox) and empty liposomes of the same composition as LipoDox showed similar skin distribution as PEGylated egg PC liposomes, suggesting that this phenomenon is relevant to liposomes of different lipid composition. Decorating liposomes with shorter PEGs (350 or 700) in addition to PEG 2000 did not decrease the deposition. Outside the capillaries, liposomes partially colocalized with CD45-, F4/80+ cells. The accumulation of liposomes was not due to prior neutrophil/platelet binding and transport across endothelium. Moreover, our studies have excluded a role of complement in the skin accumulation of liposomes. Further understanding of mechanisms of this important phenomenon can improve the safety of liposomal nanocarriers.

Indexed as

AnimalsAntineoplastic AgentsDoxorubicinDrug CarriersInjections, IntravenousIntravital MicroscopyKineticsLiposomesMice, Inbred BALB CParticle SizePolyethylene GlycolsSkinTissue DistributionAntineoplastic AgentsDoxorubicinDrug Carriersliposomal doxorubicinLiposomesPolyethylene Glycolsdoxorubicinextravasationliposomesnear-infrared fluorescencePEGskin

Identifiers

PMID29045127
PMCPMC5770233
OpenAlexW2767016552

What OpenQuestion holds

Textmetadata
LicenceTDM
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.