Evidence map›Paper›PMID 23922388›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Unique insights into the intestinal absorption, transit, and subsequent biodistribution of polymer-derived microspheres.

Joshua J Reineke, Daniel Y Cho, Yu-Ting Dingle, A Peter Morello, Jules Jacob, Christopher G Thanos, Edith Mathiowitz

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Deeply in Plasticenta: Presence of Microplastics in the Intracellular Compartment of Human Placentas.International journal of environmental research and public health · 2022
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Oral delivery of metformin by chitosan nanoparticles for polycystic kidney disease.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  16. Article
  17. Formulation technologies for oral vaccines.Clinical and experimental immunology · 2019
    Review
  18. Single Step Double-walled Nanoencapsulation (SSDN).Journal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  19. Nanoparticles for oral delivery: Design, evaluation and state-of-the-art.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  20. Review
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 at 2 institutions in 1 country.

Joshua J ReinekeDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI 48202, USA.
Daniel Y Cho
Yu-Ting Dingle
A Peter Morello
Jules Jacob
Christopher G Thanos
Edith Mathiowitz
Brown University · USEugene Applebaum College of Pharmacy and Health Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymeric microspheres (MSs) have received attention for their potential to improve the delivery of drugs with poor oral bioavailability. Although MSs can be absorbed into the absorptive epithelium of the small intestine, little is known about the physiologic mechanisms that are responsible for their cellular trafficking. In these experiments, nonbiodegradable polystyrene MSs (diameter range: 500 nm to 5 µm) were delivered locally to the jejunum or ileum or by oral administration to young male rats. Following administration, MSs were taken up rapidly (≤ 5 min) by the small intestine and were detected by transmission electron microscopy and confocal laser scanning microscopy. Gel permeation chromatography confirmed that polymer was present in all tissue samples, including the brain. These results confirm that MSs (diameter range: 500 nm to 5 µm) were absorbed by the small intestine and distributed throughout the rat. After delivering MSs to the jejunum or ileum, high concentrations of polystyrene were detected in the liver, kidneys, and lungs. The pharmacologic inhibitors chlorpromazine, phorbol 12-myristate 13-acetate, and cytochalasin D caused a reduction in the total number of MSs absorbed in the jejunum and ileum, demonstrating that nonphagocytic processes (including endocytosis) direct the uptake of MSs in the small intestine. These results challenge the convention that phagocytic cells such as the microfold cells solely facilitate MS absorption in the small intestine.

Indexed as

MicrospheresAnimalsChlorpromazineChromatography, GelCytochalasin DDrug Delivery SystemsGastrointestinal TransitIntestinal AbsorptionIntestine, SmallMaleMicroscopy, ConfocalMicroscopy, Electron, TransmissionPolystyrenesRatsTetradecanoylphorbol AcetateChlorpromazineCytochalasin DPolystyrenesTetradecanoylphorbol Acetateoral deliveryuptake mechanism

Identifiers

PMID23922388
PMCPMC3752225
OpenAlexW2035596114

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.