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PhysioMimix® is a suite of hardware, consumables and assay protocols that enable you to recreate complex human biology and accurately predict human drug responses.

PhysioMimix OOC

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Consumables

Multi-chip plates
3D validated cells
NASH-in-a-box
Bioavailability assay kit: Human 18
DILI assay kit: Human 24
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Models

Single-organ models
- Liver-on-a-chip model
- Lung-on-a-chip model
Multi-organ models
- Gut/Liver-on-a-chip models

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PhysioMimix® support packages

Discover the applications


Investigate the application areas that our PhysioMimix® products and services support

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Disease modeling

Metabolic dysfunction-associated steatohepatitis
Hepatitis B
Pulmonary infection
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Safety toxicology

Drug-induced liver injury
Immune-mediated liver injury
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ADME

Drug absorption
Drug metabolism
Drug bioavailability
Oligonucleotide delivery
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Studies as a service


Our team will work collaboratively with you to design a study around your research goals and generate actionable data within weeks

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icon-dili-tox-150x150.png Drug-induced liver injury
icon-adme-150x150.png ADME

Defining validation criteria for a primary jejunum and primary hepatocyte dual-organ MPS

July 3, 2024

Resource > Posters >

Defining validation criteria for a primary jejunum and primary hepatocyte dual-organ MPS


A promising tool for more predictive studies of human drug ADME and oral bioavailability

Filed under: ADME and Drug bioavailability

cnb1181 defining validation v1 | Gut/Liver MPS
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Improve in vitro to in vivo data translation for drug safety and efficacy with our fluidically-linked dual-organ MPS (microphysiological system); combining two well-characterized human Gut/Liver MPS – the RepliGut® Jejunum and PhysioMimix® Liver MPS, in an interconnected model suitable for enhanced bioavailability profiling.

The liver and intestinal cells are first validated separately, then as a functional, fluidically-coupled co-culture system. We then ensure all cells are metabolically suitable for ADME studies before demonstrating how the pre-clinical assay can be used to provide a deeper mechanistic understanding of a drug’s oral bioavailability in vitro, allowing drug developers to only progress the most promising therapeutic candidates through the pipeline.

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