Evidence map›Paper›PMID 18404709›Full record

ArticleJournal of biomedical materials research. Part A2009

Studies of the cellular uptake of hydrogel nanospheres and microspheres by phagocytes, vascular endothelial cells, and smooth muscle cells.

Kytai Truong Nguyen, Kajal P Shukla, Miriam Moctezuma, Arthur R C Braden, Jun Zhou, Zhibing Hu, Liping Tang

Abstract readEvaluation Study
In one paragraph

Article in Journal of biomedical materials research. Part A, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Designing of CoPharmaceutics · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Flow shear stress differentially regulates endothelial uptake of nanocarriers targeted to distinct epitopes of PECAM-1.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Article
  11. Article
  12. Article
  13. Advances in biomimetic regeneration of elastic matrix structures.Drug delivery and translational research · 2012
    Article
  14. Article
  15. Article
  16. 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

7 authors.

Kytai Truong NguyenDepartment of Bioengineering, The University of Texas at Arlington, Arlington, Texas 76019, USA.
Kajal P Shukla
Miriam Moctezuma
Arthur R C Braden
Jun Zhou
Zhibing Hu
Liping Tang

Funding

Biomaterial-mediated fibrotic responsesR01EB007271 · NIBIB · UNIVERSITY OF TEXAS ARLINGTON · PI TANG, LIPING · 2008 to 2011
$1.4M
BIOCOMPATIBILITY: SURFACE INITIATED BIOCHEMISTRYR01GM074021 · NIGMS · UNIVERSITY OF TEXAS ARLINGTON · PI TANG, LIPING · 2005 to 2007
$844k
NIBIB NIH HHS R01 EB007271NIGMS NIH HHS R01 GM074021
6 · The paper itself

Abstract

Intensive research efforts have been placed on the development of nanospheres for targeted drug delivery for treating a variety of diseases, including coronary restenosis, cancer, and inflammatory reactions. Although most of these drug-bearing spheres are delivered via intravenous administration, little is known about the effect of sphere physical characteristics on the responses of vascular and blood cells. To find the answer, this work was aimed to investigate the cellular uptake of nanosized (100 nm) and microsized hydrogel spheres (1 microm) made of poly(N-isopropylacrylamide) by vascular cells and phagocytes under various flow conditions in vitro. We found that the cellular uptake of nanospheres depended on incubation times and sphere concentrations as well as on the introduced shear stress levels of the medium. Measurements of the intracellular-released fluorescence and confocal fluorescence microscopy revealed that nanospheres were internalized by endothelial cells and smooth muscle cells more than microspheres, whereas microspheres were rapidly taken up by phagocytes, especially at high concentration. Our results strongly suggest that hydrogel nanospheres are more effective as an intravascular delivery system compared to microspheres in the terms of vascular cellular uptake and biocompatibility.

Indexed as

MicrospheresNanospheresAnimalsBiocompatible MaterialsCells, CulturedDrug CarriersDrug Delivery SystemsEndocytosisEndothelial CellsHumansHydrogelsMaleMiceMice, Inbred BALB CMyocytes, Smooth MuscleParticle SizeBiocompatible MaterialsDrug CarriersHydrogels

Identifiers

PMID18404709
PMCPMC2908386

What OpenQuestion holds

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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.