Evidence map›Paper›PMID 25011609›Full record

ArticleScientific reports2014

Tuning pharmacokinetics and biodistribution of a targeted drug delivery system through incorporation of a passive targeting component.

Rachel A Kudgus, Chad A Walden, Renee M McGovern, Joel M Reid, J David Robertson, Priyabrata Mukherjee

Abstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Trial
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  12. Conjugate of Doxorubicin to Albumin-Binding Peptide Outperforms Aldoxorubicin.Small (Weinheim an der Bergstrasse, Germany) · 2019
    Article
  13. Article
  14. Article
  15. A model-based analysis of tissue targeting efficacy of nanoparticles.Journal of the Royal Society, Interface · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Article
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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.

Rachel A KudgusDepartment of Oncology Research, Mayo Clinic, Rochester, Minnesota, United States of America.
Chad A WaldenDepartment of Oncology Research, Mayo Clinic, Rochester, Minnesota, United States of America.
Renee M McGovernDepartment of Oncology Research, Mayo Clinic, Rochester, Minnesota, United States of America.
Joel M ReidDepartment of Oncology Research, Mayo Clinic, Rochester, Minnesota, United States of America.
J David RobertsonDepartment of Chemistry and University of Missouri Research Reactor, University of Missouri, Columbia, Missouri, United States of America.
Priyabrata MukherjeeDepartment of Pathology and Peggy and Charles Stephenson Cancer Center, University of Oklahoma Health Science Center, Oklahoma City, OK, United States of America.

Funding

Molecular Mechanism of Antiangiogenic Properties of Gold NanoparticleR01CA136494 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI MUKHERJEE, PRIYABRATA · 2009 to 2020
$2.9M
Development of a gold nanoparticles based targeted delivery systemR01CA135011 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI MUKHERJEE, PRIYABRATA · 2009 to 2013
$1.5M
NCI NIH HHS CA135011NCI NIH HHS CA136494NCI NIH HHS R01 CA135011NCI NIH HHS R01 CA136494
6 · The paper itself

Abstract

Major challenges in the development of drug delivery systems (DDSs) have been the short half-life, poor bioavailability, insufficient accumulation and penetration of the DDSs into the tumor tissue. Understanding the pharmacokinetic (PK) parameters of the DDS is essential to overcome these challenges. Herein we investigate how surface chemistry affects the PK profile and organ distribution of a gold nanoparticle-based DDS containing both a passive and active targeting moiety via two common routes of administration: intravenous and intraperitoneal injections. Using LC/MS/MS, ELISA and INAA we report the half-life, peak plasma concentrations, area under the curve, ability to cross the peritoneal barrier and biodistribution of the nanoconjugates. The results highlight the design criteria for fine-tuning the PK parameters of a targeted drug delivery system that exploits the benefits of both active and passive targeting.

Indexed as

AnimalsArea Under CurveDrug Delivery SystemsGoldHalf-LifeMaleMetal NanoparticlesMiceNanoconjugatesPharmaceutical PreparationsTissue DistributionGoldNanoconjugatesPharmaceutical Preparations

Identifiers

PMID25011609
PMCPMC4092331

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.