Evidence map›Paper›PMID 31291112›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2019

Cassie-Baxter Surfaces for Reversible, Barrier-Free Integration of Microfluidics and 3D Cell Culture.

Soroosh Torabi, Linzhang Li, Jonathan Grabau, Madison Sands, Brad J Berron, Ren Xu, Christine A Trinkle

Open access · greenAbstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 1 institution in 1 country.

Soroosh TorabiMechanical Engineering , University of Kentucky , Lexington , Kentucky 40506 , United States.ORCID 0000-0001-8574-3273
Linzhang LiPharmacology and Nutritional Sciences , University of Kentucky , Lexington , Kentucky 40536 , United States.
Jonathan GrabauMechanical Engineering , University of Kentucky , Lexington , Kentucky 40506 , United States.
Madison SandsPharmacology and Nutritional Sciences , University of Kentucky , Lexington , Kentucky 40536 , United States.
Brad J BerronChemical and Materials Engineering , University of Kentucky , Lexington , Kentucky 40506 , United States.
Ren XuPharmacology and Nutritional Sciences , University of Kentucky , Lexington , Kentucky 40536 , United States.
Christine A TrinkleMechanical Engineering , University of Kentucky , Lexington , Kentucky 40506 , United States.
University of Kentucky · US

Funding

University of Kentucky Center for Cancer MetabolismP20GM121327 · NIGMS · UNIVERSITY OF KENTUCKY · PI Binhua P Zhou · 2017 to 2026
$25.0M
Roles of Hsp47 in Breast Cancer ProgressionR01CA207772 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI XU, REN · 2017 to 2025
$3.1M
Specific Lysis for Large-Volume, High-Purity Endothelial Progenitor Cell IsolatesR01HL127682 · NHLBI · UNIVERSITY OF KENTUCKY · PI BERRON, BRADLEY JOSEPH · 2015 to 2018
$2.3M
Roles of RORalpha in breast cancer development and progressionR01CA215095 · NCI · UNIVERSITY OF KENTUCKY · PI XU, REN · 2017 to 2022
$1.7M
Systemic delivery of miR-29 for basal-like breast cancer treatmentR21CA209045 · NCI · UNIVERSITY OF KENTUCKY · PI SHU, DAN, XU, REN · 2016 to 2017
$375k
NCI NIH HHS R01 CA207772NCI NIH HHS R01 CA215095NCI NIH HHS R21 CA209045NHLBI NIH HHS R01 HL127682NIGMS NIH HHS P20 GM121327
6 · The paper itself

Abstract

3D cell culture and microfluidics both represent powerful tools for replicating critical components of the cell microenvironment; however, challenges involved in the integration of the two and compatibility with standard tissue culture protocols still represent a steep barrier to widespread adoption. Here we demonstrate the use of engineered surface roughness in the form of microfluidic channels to integrate 3D cell-laden hydrogels and microfluidic fluid delivery. When a liquid hydrogel precursor solution is pipetted onto a surface containing open microfluidic channels, the solid/liquid/air interface becomes pinned at sharp edges such that the hydrogel forms the "fourth wall" of the channels upon solidification. We designed Cassie-Baxter microfluidic surfaces that leverage this phenomenon, making it possible to have barrier-free diffusion between the channels and the hydrogel; in addition, sealing is robust enough to prevent leakage between the two components during fluid flow, but the sealing can also be reversed to facilitate recovery of the cell/hydrogel material after culture. This method was used to culture MDA-MB-231 cells in collagen, which remained viable and proliferated while receiving media exclusively through the microfluidic channels over the course of several days.

Indexed as

Cell Culture TechniquesLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesCell Line, TumorHumans

Identifiers

PMID31291112
PMCPMC6996068
OpenAlexW2956389255

What OpenQuestion holds

Textmetadata
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.