Evidence map›Paper›PMID 25598505›Full record

ReviewNature reviews. Drug discovery2015

A holistic approach to targeting disease with polymeric nanoparticles.

Christopher J Cheng, Gregory T Tietjen, Jennifer K Saucier-Sawyer, W Mark Saltzman

Abstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers.

0numbers the graph read from it
0cells of the map it votes in
170citing 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

170 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Cancer chemoprevention: signaling pathways and strategic approaches.Signal transduction and targeted therapy · 2025
    Review
  13. Review
  14. Review
  15. Therapeutic Vaccination in Lung Cancer: Past Attempts, Current Approaches and Future Promises.Journal of respiratory biology and translational medicine · 2025
    Article
  16. Article
  17. Review
  18. Advanced Drug Delivery Systems: From Microsponges to Nanotechnologies.Recent advances in inflammation & allergy drug discovery · 2025
    Article
  19. Article
  20. Review

110 more citing papers are in PubMed but not listed here.

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

4 authors.

Christopher J Cheng1] Department of Biomedical Engineering, Yale University, New Haven, Connecticut 06511, USA. Present address: Alexion Pharmaceuticals, Cheshire, Connecticut 06410, USA. [2].
Gregory T Tietjen1] Department of Biomedical Engineering, Yale University, New Haven, Connecticut 06511, USA. [2].
Jennifer K Saucier-SawyerDepartment of Biomedical Engineering, Yale University, New Haven, Connecticut 06511, USA.
W Mark SaltzmanDepartment of Biomedical Engineering, Yale University, New Haven, Connecticut 06511, USA.

Funding

IMMUNOHEMATOLOGY/TRANSFUSION MEDICINE RESEARCH TRAININGT32HL007974 · NHLBI · YALE UNIVERSITY · PI JEANNE E HENDRICKSON, Diane S Krause · 2001 to 2026
$8.1M
Molecular and Cellular Transport in MucusR01EB000487 · NIBIB · YALE UNIVERSITY · PI IWASAKI, AKIKO, SALTZMAN, W. MARK · 2002 to 2019
$5.0M
CED of Nanoparticles Loading with Novel Agents for Improved Treatment of GliomasR01CA149128 · NCI · YALE UNIVERSITY · PI SALTZMAN, W. MARK · 2011 to 2020
$3.5M
In vivo genomic editing of hematopoietic cells for HIV resistanceR01AI112443 · NIAID · YALE UNIVERSITY · PI GLAZER, PETER M, KUMAR, PRITI · 2014 to 2017
$2.1M
Human and Translational ImmunologyT32AI089704 · NIAID · YALE UNIVERSITY · PI HEROLD, KEVAN C · 2010 to 2014
$994k
Molecular and Cellular Transport in MucusR56EB000487 · NIBIB · YALE UNIVERSITY · PI SALTZMAN, W. MARK · 2008 to 2008
$402k
Bioengineered siRNA/Nanoparticles to Prevent Human Transplant RejectionR56AI106922 · NIAID · YALE UNIVERSITY · PI POBER, JORDAN S, SALTZMAN, W. MARK · 2013 to 2013
$291k
Antagonizing oncogenic microRNAs for the elucidation and treatment of lymphomaF32CA174247 · NCI · YALE UNIVERSITY · PI CHENG, CHRISTOPHER JANMIN · 2013 to 2014
$72k
NCI NIH HHS CA149128NCI NIH HHS F32 CA174247NCI NIH HHS R01 CA149128NHLBI NIH HHS T32 HL007974NIAID NIH HHS AI106992NIAID NIH HHS AI112443NIAID NIH HHS R01 AI112443NIAID NIH HHS R56 AI106922NIAID NIH HHS T32 AI089704NIBIB NIH HHS EB00487NIBIB NIH HHS R01 EB000487
6 · The paper itself

Abstract

The primary goal of nanomedicine is to improve clinical outcomes. To this end, targeted nanoparticles are engineered to reduce non-productive distribution while improving diagnostic and therapeutic efficacy. Paradoxically, as this field has matured, the notion of targeting has been minimized to the concept of increasing the affinity of a nanoparticle for its target. This Opinion article outlines a holistic view of nanoparticle targeting, in which the route of administration, molecular characteristics and temporal control of the nanoparticles are potential design variables that must be considered simultaneously. This comprehensive vision for nanoparticle targeting will facilitate the integration of nanomedicines into clinical practice.

Indexed as

AnimalsDrug Delivery SystemsHumansNanomedicineNanoparticlesPolymersPolymers

Identifiers

PMID25598505
PMCPMC4451203

What OpenQuestion holds

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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.