Evidence map›Paper›PMID 22428797›Full record

ReviewCritical reviews in biomedical engineering2012

Nanoscale drug delivery systems for enhanced drug penetration into solid tumors: current progress and opportunities.

Carolyn L Waite, Charles M Roth

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in biomedical engineering, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 157 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Nanocomplexes of doxorubicin and DNA fragments for efficient and safe cancer chemotherapy.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  10. Frontiers in pharmacology · 2023
    Article
  11. Review
  12. Exosomes-mediated tumor treatment: One body plays multiple roles.Asian journal of pharmaceutical sciences · 2022
    Review
  13. Dual Size/Charge-Switchable Nanocatalytic Medicine for Deep Tumor Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  14. Kinetics of Nanomedicine in Tumor Spheroid as anFrontiers in bioengineering and biotechnology · 2021
    Review
  15. Nanomedicine : nanotechnology, biology, and medicine · 2020
    Article
  16. Review
  17. Article
  18. Biomimetic Nanomembranes: An Overview.Biomimetics (Basel, Switzerland) · 2020
    Review
  19. Article
  20. Applications of Surface Modification Technologies in Nanomedicine for Deep Tumor Penetration.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    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

2 authors at 1 institution in 1 country.

Carolyn L WaiteDepartment of Chemical and Biochemical Engineering, Rutgers University, New Brunswick, New Jersey, USA.
Charles M Roth
Rutgers, The State University of New Jersey · US

Funding

Efficient Cellular Delivery of OligonucleotidesR01EB008278 · NIBIB · RUTGERS, THE STATE UNIV OF N.J. · PI ROTH, CHARLES M. · 2009 to 2010
$688k
NIBIB NIH HHS R01 EB008278NIBIB NIH HHS R01 EB008278-07
6 · The paper itself

Abstract

Poor penetration of anticancer drags into solid tumors significantly limits their efficacy. This phenomenon has long been observed for small-molecule chemotherapeutics, and it can be even more pronounced for nanoscale therapies. Nanoparticles have enormous potential for the treatment of cancer due to their wide applicability as drug delivery and imaging vehicles and their size-dependent accumulation into solid tumors by the enhanced permeability and retention (EPR) effect. Further, synthetic nanoparticles can be engineered to overcome barriers to drag delivery. Despite their promise for the treatment of cancer, relatively little work has been done to study and improve their ability to diffuse into solid tumors following passive accumulation in the tumor vasculature. In this review, we present the complex issues governing efficient penetration of nanoscale therapies into solid tumors. The current methods available to researchers to study nanoparticle penetration into malignant tumors are described, and the most recent works studying the penetration of nanoscale materials into solid tumors are summarized. We conclude with an overview of the important nanoparticle design parameters governing their tumor penetration, as well as by highlighting critical directions in this field.

Indexed as

Antineoplastic AgentsHumansNanocapsulesNanomedicineNeoplasmsAntineoplastic AgentsNanocapsules

Identifiers

PMID22428797
PMCPMC3639314
OpenAlexW2123660822

What OpenQuestion holds

Textmetadata
LicenceTDM
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.