Evidence map›Paper›PMID 36649249›Full record

ArticlePloS one2023

Spatially selective cell treatment and collection for integrative drug testing using hydrodynamic flow focusing and shifting.

Xu Wang, Jingtian Zheng, Maheshwar Adiraj Iyer, Adam Henry Szmelter, David T Eddington, Steve Seung-Young Lee

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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 at 2 institutions in 1 country.

Xu WangDepartment of Pharmaceutical Sciences, University of Illinois Chicago, Chicago, Illinois, United States of America.
Jingtian ZhengDepartment of Pharmaceutical Sciences, University of Illinois Chicago, Chicago, Illinois, United States of America.
Maheshwar Adiraj IyerDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, Illinois, United States of America.
Adam Henry SzmelterDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, Illinois, United States of America.
David T EddingtonDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, Illinois, United States of America.
Steve Seung-Young LeeDepartment of Pharmaceutical Sciences, University of Illinois Chicago, Chicago, Illinois, United States of America.ORCID 0000-0003-1349-3759
University of Illinois Chicago · USUniversity of Illinois Urbana-Champaign · US

Funding

Integrated three-dimensional (3D) microscopy for a spatial pharmacology atlas of macromolecular drugs in the tissue microenvironmentR35GM142743 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LEE, STEVE SEUNG-YOUNG · 2021 to 2025
$2.3M
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR015482 · NCRR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BAUMAN, JERRY L · 2000 to 2000
$909k
Transparent Tumor Tomography (T3): Multi-Parameter 3D Imaging for Tumor ImmunotherapyR00EB022636 · NIBIB · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LEE, STEVE SEUNG-YOUNG · 2019 to 2021
$747k
NCRR NIH HHS C06 RR015482NIBIB NIH HHS R00 EB022636NIGMS NIH HHS R35 GM142743
6 · The paper itself

Abstract

Hydrodynamic focusing capable of readily producing and controlling laminar flow facilitates drug treatment of cells in existing microfluidic culture devices. However, to expand applications of such devices to multiparameter drug testing, critical limitations in current hydrodynamic focusing microfluidics must be addressed. Here we describe hydrodynamic focusing and shifting as an advanced microfluidics tool for spatially selective drug delivery and integrative cell-based drug testing. We designed and fabricated a co-flow focusing, three-channel microfluidic device with a wide cell culture chamber. By controlling inlet flow rates of sample and two side solutions, we could generate hydrodynamic focusing and shifting that mediated precise regulation of the path and width of reagent and drug stream in the microfluidic device. We successfully validated a hydrodynamic focusing and shifting approach for spatially selective delivery of DiI, a lipophilic fluorophore, and doxorubicin, a chemotherapeutic agent, to tumor cells in our device. Moreover, subsequent flowing of a trypsin EDTA solution over the cells that were exposed to doxorubicin flow allowed us to selectively collect the treated cells. Our approach enabled downstream high-resolution microscopy of the cell suspension to confirm the nuclear delivery of doxorubicin into the tumor cells. In the device, we could also evaluate in situ the cytotoxic effect of doxorubicin to the tumor cells that were selectively treated by hydrodynamic flow focusing and shifting. These results show that hydrodynamic focusing and shifting enable a fast and robust approach to spatially treat and then collect cells in an optimized microfluidic device, offering an integrative assay tool for efficient drug screening and discovery.

Indexed as

HydrodynamicsMicrofluidic Analytical TechniquesDrug Delivery SystemsFluorescent DyesMicrofluidicsSubstance Abuse DetectionFluorescent Dyes

Identifiers

PMID36649249
PMCPMC9844832
OpenAlexW4316928028

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.