Evidence map›Paper›PMID 25599856›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2015

Synthetic tumor networks for screening drug delivery systems.

Balabhaskar Prabhakarpandian, Ming-Che Shen, Joseph B Nichols, Charles J Garson, Ivy R Mills, Majed M Matar, Jason G Fewell, Kapil Pant

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2015. 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
5.4field-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

22 citing papers in PubMed, 56 citations in OpenAlex.

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  18. In vitro microfluidic models of tumor microenvironment to screen transport of drugs and nanoparticles.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Balabhaskar PrabhakarpandianBiomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA. Electronic address: bxp@cfdrc.com.
Ming-Che ShenBiomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA.
Joseph B NicholsBiomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA.
Charles J GarsonBiomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA.
Ivy R MillsBiomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA.
Majed M MatarCelsion-EGEN, Huntsville, AL 35806, USA.
Jason G FewellCelsion-EGEN, Huntsville, AL 35806, USA.
Kapil PantBiomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA.
CFD Research Corporation (United States) · USCelsion (United States) · US

Funding

A Novel Microfluidic Device for Selection and Optimization of Drug Delivery VehicR43CA139841 · NCI · CFD RESEARCH CORPORATION · PI PRABHAKARPANDIAN, BALABHASKAR · 2009 to 2009
$158k
NCI NIH HHS 1R43CA139841-01NCI NIH HHS R43 CA139841
6 · The paper itself

Abstract

Tumor drug delivery is a complex phenomenon affected by several elements in addition to drug or delivery vehicle's physico-chemical properties. A key factor is tumor microvasculature with complex effects including convective transport, high interstitial pressure and enhanced vascular permeability due to the presence of "leaky vessels". Current in vitro models of the tumor microenvironment for evaluating drug delivery are oversimplified and, as a result, show poor correlation with in vivo performance. In this study, we report on the development of a novel microfluidic platform that models the tumor microenvironment more accurately, with physiologically and morphologically realistic microvasculature including endothelial cell lined leaky capillary vessels along with 3D solid tumors. Endothelial cells and 3D spheroids of cervical tumor cells were co-cultured in the networks. Drug vehicle screening was demonstrated using GFP gene delivery by different formulations of nanopolymers. The synthetic tumor network was successful in predicting in vivo delivery efficiencies of the drug vehicles. The developed assay will have critical applications both in basic research, where it can be used to develop next generation delivery vehicles, and in drug discovery where it can be used to study drug transport and delivery efficacy in realistic tumor microenvironment, thereby enabling drug compound and/or delivery vehicle screening.

Indexed as

Drug Delivery SystemsTumor MicroenvironmentCell LineCoculture TechniquesEndothelial CellsGene Transfer TechniquesGreen Fluorescent ProteinsHeLa CellsHumansMicrofluidicsNanoparticlesNeoplasmsPlasmidsPolymersGreen Fluorescent ProteinsPolymersGene deliveryMicrofluidicsMicrovasculatureNanopolymersTumors

Identifiers

PMID25599856
PMCPMC4418523
OpenAlexW2047762633

What OpenQuestion holds

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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.