Evidence map›Paper›PMID 30358386›Full record

ArticleAnalytical chemistry2018

A Plug-and-Play, Drug-on-Pillar Platform for Combination Drug Screening Implemented by Microfluidic Adaptive Printing.

Jiannan Li, Wen Tan, Wenwu Xiao, Randy P Carney, Yongfan Men, Yuanpei Li, Gerald Quon, Yousif Ajena, Kit S Lam, Tingrui Pan

Abstract read
In one paragraph

Article in Analytical chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  9. Article
  10. High-Throughput Experimentation Using Cell-Free Protein Synthesis Systems.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  11. Article
  12. 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

10 authors.

Jiannan LiMicro-Nano Innovations (MiNI) Laboratory, Department of Biomedical Engineering and Department of Electrical and Computer Engineering , University of California , Davis , California 95616 , United States.ORCID 0000-0002-6089-4785
Wen TanMicro-Nano Innovations (MiNI) Laboratory, Department of Biomedical Engineering and Department of Electrical and Computer Engineering , University of California , Davis , California 95616 , United States.
Wenwu XiaoDepartment of Biochemistry and Molecular Medicine, School of Medicine, UC Davis NCI-designated Comprehensive Cancer Center , University of California Davis , Sacramento , California 95817 , United States.
Randy P CarneyDepartment of Biochemistry and Molecular Medicine, School of Medicine, UC Davis NCI-designated Comprehensive Cancer Center , University of California Davis , Sacramento , California 95817 , United States.
Yongfan MenMicro-Nano Innovations (MiNI) Laboratory, Department of Biomedical Engineering and Department of Electrical and Computer Engineering , University of California , Davis , California 95616 , United States.
Yuanpei LiDepartment of Biochemistry and Molecular Medicine, School of Medicine, UC Davis NCI-designated Comprehensive Cancer Center , University of California Davis , Sacramento , California 95817 , United States.ORCID 0000-0002-4015-646X
Gerald QuonDepartment of Molecular and Cellular Biology , University of California , Davis , California 95616 , United States.
Yousif AjenaDepartment of Biochemistry and Molecular Medicine, School of Medicine, UC Davis NCI-designated Comprehensive Cancer Center , University of California Davis , Sacramento , California 95817 , United States.
Kit S LamDepartment of Biochemistry and Molecular Medicine, School of Medicine, UC Davis NCI-designated Comprehensive Cancer Center , University of California Davis , Sacramento , California 95817 , United States.ORCID 0000-0002-3076-6969
Tingrui PanMicro-Nano Innovations (MiNI) Laboratory, Department of Biomedical Engineering and Department of Electrical and Computer Engineering , University of California , Davis , California 95616 , United States.

Funding

Workshop on Environmental Technology Transfer and EntrepreneurshipP42ES004699 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1987 to 2021
$50.1M
Therapeutic Targeting Agents for Ovarian CancerR01CA115483 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI LAM, KIT S · 2005 to 2019
$5.5M
Targeting nanotherapeutics against murine and feline oral cancerR01EB012569 · NIBIB · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LAM, KIT S · 2011 to 2019
$4.2M
Digital one-disc-one-compound array for high-throughput discovery of cancer-targeR21CA173243 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PAN, TINGRUI · 2013 to 2015
$644k
NCI NIH HHS R01 CA115483NCI NIH HHS R21 CA173243NIBIB NIH HHS R01 EB012569NIEHS NIH HHS P42 ES004699
6 · The paper itself

Abstract

Traditional high-throughput drug combination screening requires automatic pipetting of drugs into high-density microtiter plates. Here, a drug-on-pillar platform is proposed for efficient combination drug screening. Using the proposed approach, combination drug screening can be carried out in a plug-and-play manner, allowing for high-throughput screening of large permutations of drug combinations at various concentrations, such that drug dispensing and cell-based screening can be temporally separated and therefore can potentially be performed at distant laboratories. The dispensing is implemented using our recently developed microfluidic pneumatic printing platform, which features a low-cost disposable cartridge that minimizes cross contamination. Moreover, our previously developed drug nanoformulation method with amphiphilic telodendrimers has been utilized to maintain drug stability in a dry form, allowing for convenient drug storage, shipping, and subsequent rehydration. Combining the features described above, we have implemented a 1260-spot drug combination array to study the effect of paired drugs against MDA-MB-231 triple negative human breast cancer cells. This study supports the feasibility of the drug-on-pillar platform for combination drug screening and has provided valuable insight into drug combination efficacy against breast cancer.

Indexed as

Microfluidic Analytical TechniquesPrinting, Three-DimensionalAntineoplastic AgentsCell ProliferationCell SurvivalDose-Response Relationship, DrugDoxorubicinDrug CombinationsDrug Evaluation, PreclinicalDrug Screening Assays, AntitumorHumansStructure-Activity RelationshipTriple Negative Breast NeoplasmsTumor Cells, CulturedAntineoplastic AgentsDoxorubicinDrug Combinations

Identifiers

PMID30358386
PMCPMC6467812

What OpenQuestion holds

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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.