Evidence map›Paper›PMID 23211088›Full record

ArticleMolecular pharmaceutics2013

Novel, biocompatible, and disease modifying VIP nanomedicine for rheumatoid arthritis.

Varun Sethi, Israel Rubinstein, Antonina Kuzmis, Helen Kastrissios, James Artwohl, Hayat Onyuksel

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 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
1.8field-weighted citation impact, top 15% 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, 49 citations in OpenAlex.

  1. Research Progress of SN38 Drug Delivery System in Cancer Treatment.International journal of nanomedicine · 2024
    Review
  2. Article
  3. Peptide Helix-YPPAR research · 2023
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. GLP-1 nanomedicine alleviates gut inflammation.Nanomedicine : nanotechnology, biology, and medicine · 2017
    Article
  17. When Is It Important to Measure Unbound Drug in Evaluating Nanomedicine Pharmacokinetics?Drug metabolism and disposition: the biological fate of chemicals · 2016
    Review
  18. Particle-based technologies for osteoarthritis detection and therapy.Drug delivery and translational research · 2016
    Review
  19. Article
  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

6 authors at 2 institutions in 1 country.

Varun SethiDepartment of Biopharmaceutical Sciences, Jesse Brown VA Medical Center, Chicago, Illinois 60612, United States.
Israel Rubinstein
Antonina Kuzmis
Helen Kastrissios
James Artwohl
Hayat Onyuksel
University of Illinois Chicago · USJesse Brown VA Medical Center · US

Funding

Novel Biomarkers of COPD - Parma SiteR01HL072323 · NHLBI · UNIVERSITY OF PARMA · PI MUTTI, ANTONIO · 2002 to 2005
$1.5M
Phospholipid Nanocarriers Improve Chemotherapy by Targeted Drug DeliveryR01CA121797 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ONYUKSEL, HAYAT · 2007 to 2010
$1.2M
Micellar VIP Nanoparticles for Rheumatoid ArthritisR01AG024026 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RUBINSTEIN, ISRAEL · 2004 to 2007
$1.1M
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR015482 · NCRR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BAUMAN, JERRY L · 2000 to 2000
$909k
NCI NIH HHS CA121797NCI NIH HHS R01 CA121797NCRR NIH HHS C06 RR015482NCRR NIH HHS C06RR15482NHLBI NIH HHS HL72343NHLBI NIH HHS R01 HL072323NIA NIH HHS AG024026NIA NIH HHS R01 AG024026
6 · The paper itself

Abstract

Despite advances in rheumatoid arthritis (RA) treatment, efficacious and safe disease-modifying therapy still represents an unmet medical need. Here, we describe an innovative strategy to treat RA by targeting low doses of vasoactive intestinal peptide (VIP) self-associated with sterically stabilized micelles (SSMs). This spontaneous interaction of VIP with SSM protects the peptide from degradation or inactivation in biological fluids and prolongs circulation half-life. Treatment with targeted low doses of nanosized SSM-VIP but not free VIP in buffer significantly reduced the incidence and severity of arthritis in an experimental model, completely abrogating joint swelling and destruction of cartilage and bone. In addition, SSM associated VIP, unlike free VIP, had no side-effects on the systemic functions due to selective targeting to inflamed joints. Finally, low doses of VIP in SSM successfully downregulated both inflammatory and autoimmune components of RA. Collectively, our data clearly indicate that VIP-SSM should be developed to be used as a novel nanomedicine for the treatment of RA.

Indexed as

MicellesAnimalsArthritis, RheumatoidInflammationMaleMiceNanomedicinePhospholipidsVasoactive Intestinal PeptideMicellesPhospholipidsVasoactive Intestinal Peptide

Identifiers

PMID23211088
PMCPMC3563715
OpenAlexW2044414574

What OpenQuestion holds

Textmetadata
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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.