Evidence map›Paper›PMID 32583981›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2020

Cellular Interactions of Liposomes and PISA Nanoparticles during Human Blood Flow in a Microvascular Network.

Mai N Vu, Hannah G Kelly, Adam K Wheatley, Scott Peng, Emily H Pilkington, Nicholas A Veldhuis, Thomas P Davis, Stephen J Kent, Nghia P Truong

Open access · bronzeAbstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 88 citations in OpenAlex.

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  12. A Review of in vivo Toxicity of Quantum Dots in Animal Models.International journal of nanomedicine · 2023
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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

9 authors at 1 institution in 2 countries.

Mai N VuAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.
Hannah G KellyAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.
Adam K WheatleyAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.
Scott PengAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.
Emily H PilkingtonAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.
Nicholas A VeldhuisAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.
Thomas P DavisAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.ORCID https://orcid.org/0000-0003-2581-4986
Stephen J KentAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.ORCID https://orcid.org/0000-0002-8539-4891
Nghia P TruongAustralian Research Council Centre of Excellence in Convergent Bio-Nano Science and Technology, Parkville, VIC, 3052, Australia.ORCID https://orcid.org/0000-0001-9900-2644
Australian Research Council · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key concept in nanomedicine is encapsulating therapeutic or diagnostic agents inside nanoparticles to prolong blood circulation time and to enhance interactions with targeted cells. During circulation and depending on the selected application (e.g., cancer drug delivery or immune modulators), nanoparticles are required to possess low or high interactions with cells in human blood and blood vessels to minimize side effects or maximize delivery efficiency. However, analysis of cellular interactions in blood vessels is challenging and is not yet realized due to the diverse components of human blood and hemodynamic flow in blood vessels. Here, the first comprehensive method to analyze cellular interactions of both synthetic and commercially available nanoparticles under human blood flow conditions in a microvascular network is developed. Importantly, this method allows to unravel the complex interplay of size, charge, and type of nanoparticles on their cellular associations under the dynamic flow of human blood. This method offers a unique platform to study complex interactions of any type of nanoparticles in human blood flow conditions and serves as a useful guideline for the rational design of liposomes and polymer nanoparticles for diverse applications in nanomedicine.

Indexed as

LiposomesNanoparticlesHemodynamicsHumansMicrovesselsPolymerizationLiposomesblood flowcellular interactionsfresh human bloodliposomesPISA nanoparticlespolymerization-induced self-assemblyreversible addition-fragmentation chain transfer (RAFT)

Identifiers

PMID32583981
PMCPMC7361276
OpenAlexW3037861502

What OpenQuestion holds

Textmetadata
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.