Evidence map›Paper›PMID 24647104›Full record

ArticlePharmaceutics2014

Application of pharmacokinetic and pharmacodynamic analysis to the development of liposomal formulations for oncology.

Sihem Ait-Oudhia, Donald E Mager, Robert M Straubinger

Abstract read
In one paragraph

Article in Pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Review
  2. A Novel Liposomal In-Situ Hydrogel Formulation ofGels (Basel, Switzerland) · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Pharmacokinetic behaviors of soft nanoparticulate formulations of chemotherapeutics.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

3 authors.

Sihem Ait-OudhiaDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, Amherst, NY 14214, USA. Sihema@buffalo.edu.
Donald E MagerDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, Amherst, NY 14214, USA. dmager@buffalo.edu.
Robert M StraubingerDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, Amherst, NY 14214, USA. rms@buffalo.edu.

Funding

Pancreas cancer combination therapy based on stromal modulators and nano-carriersR21CA168454 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MA, WEN WEE, STRAUBINGER, ROBERT M · 2012 to 2013
$396k
NCI NIH HHS R21 CA168454
6 · The paper itself

Abstract

Liposomal formulations of anticancer agents have been developed to prolong drug circulating lifetime, enhance anti-tumor efficacy by increasing tumor drug deposition, and reduce drug toxicity by avoiding critical normal tissues. Despite the clinical approval of numerous liposome-based chemotherapeutics, challenges remain in the development and clinical deployment of micro- and nano-particulate formulations, as well as combining these novel agents with conventional drugs and standard-of-care therapies. Factors requiring optimization include control of drug biodistribution, release rates of the encapsulated drug, and uptake by target cells. Quantitative mathematical modeling of formulation performance can provide an important tool for understanding drug transport, uptake, and disposition processes, as well as their role in therapeutic outcomes. This review identifies several relevant pharmacokinetic/pharmacodynamic models that incorporate key physical, biochemical, and physiological processes involved in delivery of oncology drugs by liposomal formulations. They capture observed data, lend insight into factors determining overall antitumor response, and in some cases, predict conditions for optimizing chemotherapy combinations that include nanoparticulate drug carriers.

Identifiers

PMID24647104
PMCPMC3978529

What OpenQuestion holds

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Registered trials

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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.