Evidence map›Paper›PMID 18510429›Full record

ReviewNanomedicine (London, England)2008

Design opportunities for actively targeted nanoparticle vaccines.

Tarek M Fahmy, Stacey L Demento, Michael J Caplan, Ira Mellman, W Mark Saltzman

Abstract readReview
In one paragraph

Review in Nanomedicine (London, England), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Nanotechnology for delivery of peptide nucleic acids (PNAs).Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  9. Review
  10. Multifunctional nanoparticles for cancer immunotherapy.Human vaccines & immunotherapeutics · 2016
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Utilization of biodegradable polymeric materials as delivery agents in dermatology.Clinical, cosmetic and investigational dermatology · 2014
    Review
  16. Article
  17. Article
  18. Advances in biomimetic regeneration of elastic matrix structures.Drug delivery and translational research · 2012
    Article
  19. Article
  20. Enhancement of surface ligand display on PLGA nanoparticles with amphiphilic ligand conjugates.Journal of controlled release : official journal of the Controlled Release Society · 2011
    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

5 authors.

Tarek M FahmyYale University, Department of Biomedical Engineering, USA. tarek.fahmy@yale.edu
Stacey L Demento
Michael J Caplan
Ira Mellman
W Mark Saltzman

Funding

Molecular and Cellular Transport in MucusR01EB000487 · NIBIB · YALE UNIVERSITY · PI IWASAKI, AKIKO, SALTZMAN, W. MARK · 2002 to 2019
$5.0M
Molecular and Cellular Transport in MucusR56EB000487 · NIBIB · YALE UNIVERSITY · PI SALTZMAN, W. MARK · 2008 to 2008
$402k
NIBIB NIH HHS EB000487NIBIB NIH HHS R01 EB000487NIBIB NIH HHS R56 EB000487
6 · The paper itself

Abstract

Vaccines for many infectious diseases are poorly developed or simply unavailable. There are significant technological and practical design issues that contribute to this problem; thus, a solution to the vaccine problem will require a systematic approach to test the multiple variables that are required to address each of the design challenges. Nanoparticle technology is an attractive methodology for optimizing vaccine development because design variables can be tested individually or in combination. The biology of individual components that constitute an effective vaccine is often well understood and may be integrated into particle design, affording optimal immune responses to specific pathogens. Here, we review technological variables and design parameters associated with creating modular nanoparticle vaccine systems that can be used as vectors to protect against disease. Variables, such as the material and size of the core matrix, surface modification for attaching targeting ligands and routes of administration, are discussed. Optimization of these variables is important for the development of nanoparticle-based vaccine systems against infectious diseases and cancer.

Indexed as

Drug DesignDrug Delivery SystemsNanomedicineNanostructuresVaccinesVaccines

Identifiers

PMID18510429
PMCPMC5545123

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.