Evidence map›Paper›PMID 39213819›Full record

ArticleBiosensors & bioelectronics2024

Organ chips with integrated multifunctional sensors enable continuous metabolic monitoring at controlled oxygen levels.

Zohreh Izadifar, Berenice Charrez, Micaela Almeida, Stijn Robben, Kanoelani Pilobello, Janet van der Graaf-Mas, Susan L Marquez, Thomas C Ferrante, Kostyantyn Shcherbina, Russell Gould and 3 more

Abstract read
In one paragraph

Article in Biosensors & bioelectronics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

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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

13 authors.

Zohreh IzadifarWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Berenice CharrezWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Micaela AlmeidaWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Stijn RobbenWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA; Department of Microelectronics, Technical University Delft, Delft, 2628 CD, Netherlands.
Kanoelani PilobelloWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Janet van der Graaf-MasWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Susan L MarquezWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Thomas C FerranteWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Kostyantyn ShcherbinaWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Russell GouldWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Nina T LoGrandeWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Adama M SesayWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA.
Donald E IngberWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02215, USA; Vascular Biology Program and Department of Surgery, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA; Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA. Electronic address: don.ingber@wyss.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite remarkable advances in Organ-on-a-chip (Organ Chip) microfluidic culture technology, recreating tissue-relevant physiological conditions, such as the region-specific oxygen concentrations, remains a formidable technical challenge, and analysis of tissue functions is commonly carried out using one analytical technique at a time. Here, we describe two-channel Organ Chip microfluidic devices fabricated from polydimethylsiloxane and gas impermeable polycarbonate materials that are integrated with multiple sensors, mounted on a printed circuit board and operated using a commercially available Organ Chip culture instrument. The novelty of this system is that it enables the recreation of physiologically relevant tissue-tissue interfaces and oxygen tension as well as non-invasive continuous measurement of transepithelial electrical resistance, oxygen concentration and pH, combined with simultaneous analysis of cellular metabolic activity (ATP/ADP ratio), cell morphology, and tissue phenotype. We demonstrate the reliable and reproducible functionality of this system in living human Gut and Liver Chip cultures. Changes in tissue barrier function and oxygen tension along with their functional and metabolic responses to chemical stimuli (e.g., calcium chelation, oligomycin) were continuously and noninvasively monitored on-chip for up to 23 days. A physiologically relevant microaerobic microenvironment that supports co-culture of human intestinal cells with living Lactococcus lactis bacteria also was demonstrated in the Gut Chip. The integration of multi-functional sensors into Organ Chips provides a robust and scalable platform for the simultaneous, continuous, and non-invasive monitoring of multiple physiological functions that can significantly enhance the comprehensive and reliable evaluation of engineered tissues in Organ Chip models in basic research, preclinical modeling, and drug development.

Indexed as

Biosensing TechniquesLab-On-A-Chip DevicesOxygenCaco-2 CellsEquipment DesignHumansLiverMicrophysiological SystemsOxygenMetabolic sensingOrgan-on-a-chipOxygenpHSensorTransepithelial electrical resistance

Identifiers

PMID39213819
PMCPMC11391946

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.