Evidence map›Paper›PMID 19852512›Full record

ArticleMolecular pharmaceutics

Impact of hydrogel nanoparticle size and functionalization on in vivo behavior for lung imaging and therapeutics.

Yongjian Liu, Aida Ibricevic, Joel A Cohen, Jessica L Cohen, Sean P Gunsten, Jean M J Fréchet, Michael J Walter, Michael J Welch, Steven L Brody

Abstract read
In one paragraph

Article in Molecular pharmaceutics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

  1. Pooled it
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  18. Polymeric nanoparticles in development for treatment of pulmonary infectious diseases.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2016
    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

9 authors at 1 institution in 1 country.

Yongjian LiuDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Aida Ibricevic
Joel A Cohen
Jessica L Cohen
Sean P Gunsten
Jean M J Fréchet
Michael J Walter
Michael J Welch
Steven L Brody
University of California, Berkeley · US

Funding

SYNTHESIS COMPONENTU01HL080729 · NHLBI · WASHINGTON UNIVERSITY · PI ACKERMAN, JOSEPH J. H. · 2005 to 2009
$12.1M
RESEARCH RESOURCE IN RADIONUCLIDE RESEARCHR24CA086307 · NCI · WASHINGTON UNIVERSITY · PI WELCH, MICHAEL J. · 1999 to 2009
$8.4M
Nanoscale delivery vehicles for antigen-based vaccinesR01EB005824 · NIBIB · UNIVERSITY OF CALIFORNIA BERKELEY · PI FRECHET, JEAN M · 2005 to 2008
$2.0M
NCI NIH HHS CA86307NCI NIH HHS R24 CA086307NHLBI NIH HHS U01 HL080729NHLBI NIH HHS U01HL080729NIBIB NIH HHS R01 EB005824NIBIB NIH HHS R01-EB005824
6 · The paper itself

Abstract

Polymer chemistry offers the possibility of synthesizing multifunctional nanoparticles which incorporate moieties that enhance diagnostic and therapeutic targeting of cargo delivery to the lung. However, since rules for predicting particle behavior following modification are not well-defined, it is essential that probes for tracking fate in vivo are also included. Accordingly, we designed polyacrylamide-based hydrogel particles of differing sizes, functionalized with a nona-arginine cell-penetrating peptide (Arg(9)), and labeled with imaging components to assess lung retention and cellular uptake after intratracheal administration. Radiolabeled microparticles (1-5 microm diameter) and nanoparticles (20-40 nm diameter) without and with Arg(9) showed diffuse airspace distribution by positron emission tomography imaging. Biodistribution studies revealed that particle clearance and extrapulmonary distribution was, in part, size dependent. Microparticles were rapidly cleared by mucociliary routes but, unexpectedly, also through the circulation. In contrast, nanoparticles had prolonged lung retention enhanced by Arg(9) and were significantly restricted to the lung. For all particle types, uptake was predominant in alveolar macrophages and, to a lesser extent, lung epithelial cells. In general, particles did not induce local inflammatory responses, with the exception of microparticles bearing Arg(9). Whereas microparticles may be advantageous for short-term applications, nanosized particles constitute an efficient high-retention and non-inflammatory vehicle for the delivery of diagnostic imaging agents and therapeutics to lung airspaces and alveolar macrophages that can be enhanced by Arg(9). Importantly, our results show that minor particle modifications may significantly impact in vivo behavior within the complex environments of the lung, underscoring the need for animal modeling.

Indexed as

Lung DiseasesAcrylic ResinsAnimalsCell LineDiagnostic ImagingFlow CytometryHumansHydrogel, Polyethylene Glycol DimethacrylateLungMacrophages, AlveolarMiceMice, Inbred C57BLMicroscopy, Electron, ScanningModels, TheoreticalNanoparticlesParticle SizeAcrylic ResinsHydrogel, Polyethylene Glycol DimethacrylatePolyacrylamides

Identifiers

PMID19852512
PMCPMC2804872
OpenAlexW2017155154

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.