Evidence map›Paper›PMID 19896996›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2010

Claudin 4-targeted protein incorporated into PLGA nanoparticles can mediate M cell targeted delivery.

Thejani E Rajapaksa, Mary Stover-Hamer, Xiomara Fernandez, Holly A Eckelhoefer, David D Lo

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 135 citations in OpenAlex.

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  11. Functionalized nanoparticles targeting biomarkers for prostate cancer imaging and therapy.American journal of clinical and experimental urology · 2022
    Review
  12. Emerging Theranostic Nanomaterials in Diabetes and Its Complications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  13. Review
  14. Imbalance of autophagy and apoptosis in intestinal epithelium lacking the vitamin D receptor.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
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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

5 authors at 1 institution in 1 country.

Thejani E RajapaksaDivision of Biomedical Sciences, University of California, Riverside, CA 92521, USA.
Mary Stover-Hamer
Xiomara Fernandez
Holly A Eckelhoefer
David D Lo
University of California, Riverside · US

Funding

Genes regulating M cell differentiationR01AI063426 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI LO, DAVID D · 2005 to 2016
$3.6M
Mucosal M Cell Endocytosis: Specificity and MechanismsR21AI073689 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI LO, DAVID D · 2007 to 2008
$409k
FAE specific receptors for targeted vaccine deliveryR43AI058434 · NIAID · NEUROME, INC. · PI LO, DAVID D · 2004 to 2004
$316k
NIAID NIH HHS AI73689NIAID NIH HHS R01 AI063426NIAID NIH HHS R21 AI073689NIAID NIH HHS R43 AI058434
6 · The paper itself

Abstract

Polymer-based microparticles are in clinical use mainly for their ability to provide controlled release of peptides and compounds, but they are also being explored for their potential to deliver vaccines and drugs as suspensions directly into mucosal sites. It is generally assumed that uptake is mediated by epithelial M cells, but this is often not directly measured. To study the potential for optimizing M cell uptake of polymer microparticles in vivo, we produced sub-micron size PLGA particles incorporating a recombinant protein. This recombinant protein was produced with or without a c-terminal peptide previously shown to have high affinity binding to Claudin 4, a protein associated with M cell endocytosis. While the PLGA nanoparticles incorporate the protein throughout the matrix, much of the protein was also displayed on the surface, allowing us to take advantage of the binding activity of the targeting peptide. Accordingly, we found that instillation of these nanoparticles into the nasal passages or stomach of mice was found to significantly enhance their uptake by upper airway and intestinal M cells. Our results suggest that a reasonably simple nanoparticle manufacture method can provide insight into developing an effective needle-free delivery system.

Indexed as

AnimalsBiological TransportCell LineCHO CellsClaudin-4CricetinaeCricetulusDrug CarriersHemagglutininsInfluenza A virusLactic AcidMembrane ProteinsMiceMucous MembraneNanoparticlesPeyer's PatchesClaudin-4Cldn4 protein, mouseDrug CarriersHemagglutininsLactic AcidMembrane ProteinsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerRecombinant Proteins

Identifiers

PMID19896996
PMCPMC2823968
OpenAlexW1973426656

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.