Evidence map›Paper›PMID 22456798›Full record

ArticleLab on a chip2012

A programmable microfluidic cell array for combinatorial drug screening.

Jeongyun Kim, David Taylor, Nitin Agrawal, Han Wang, Hyunsoo Kim, Arum Han, Kaushal Rege, Arul Jayaraman

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

54 citing papers in PubMed, 164 citations in OpenAlex.

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  6. A novel array-type microdroplet parallel-generation device.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2023
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  15. Oncoimmunology Meets Organs-on-Chip.Frontiers in molecular biosciences · 2021
    Review
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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

8 authors at 3 institutions in 1 country.

Jeongyun KimDepartment of Chemical Engineering, Texas A&M University, College Station, TX 77843-3122, USA.
David Taylor
Nitin Agrawal
Han Wang
Hyunsoo Kim
Arum Han
Kaushal Rege
Arul Jayaraman
Texas A&M University · USArizona State University · USPacific Northwest National Laboratory · US

Funding

Microfluidics-Based Platform for Screening Combinatorial Drug TreatmentsR21CA131891 · NCI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI JAYARAMAN, ARUL, REGE, KAUSHAL · 2008 to 2009
$375k
NCI NIH HHS 5R21CA131891-02NCI NIH HHS R21 CA131891
6 · The paper itself

Abstract

We describe the development of a fully automatic and programmable microfluidic cell culture array that integrates on-chip generation of drug concentrations and pair-wise combinations with parallel culture of cells for drug candidate screening applications. The device has 64 individually addressable cell culture chambers in which cells can be cultured and exposed either sequentially or simultaneously to 64 pair-wise concentration combinations of two drugs. For sequential exposure, a simple microfluidic diffusive mixer is used to generate different concentrations of drugs from two inputs. For generation of 64 pair-wise combinations from two drug inputs, a novel time dependent variable concentration scheme is used in conjunction with the simple diffusive mixer to generate the desired combinations without the need for complex multi-layer structures or continuous medium perfusion. The generation of drug combinations and exposure to specific cell culture chambers are controlled using a LabVIEW interface capable of automatically running a multi-day drug screening experiment. Our cell array does not require continuous perfusion for keeping cells exposed to concentration gradients, minimizing the amount of drug used per experiment, and cells cultured in the chamber are not exposed to significant shear stress continuously. The utility of this platform is demonstrated for inducing loss of viability of PC3 prostate cancer cells using combinations of either doxorubicin or mitoxantrone with TRAIL (TNF-alpha Related Apoptosis Inducing Ligand) either in a sequential or simultaneous format. Our results demonstrate that the device can capture the synergy between different sensitizer drugs and TRAIL and demonstrate the potential of the microfluidic cell array for screening and optimizing combinatorial drug treatments for cancer therapy.

Indexed as

Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCell Culture TechniquesCell Line, TumorCell SurvivalCombinatorial Chemistry TechniquesDrug CombinationsDrug Evaluation, PreclinicalDrug SynergismHumansMaleMicrofluidic Analytical TechniquesProstatic NeoplasmsTNF-Related Apoptosis-Inducing LigandAntineoplastic AgentsDrug CombinationsTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, human

Identifiers

PMID22456798
PMCPMC11656301
OpenAlexW2104645521

What OpenQuestion holds

Textmetadata
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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.