Cross-flow membrane chip - Organ-on-Chip and more Fluidic 480

The Fluidic 480 Organ-on-a-Chip by Microfluidic ChipShop is an affordable and compact solution for recreating in vitro biological barriers. Each chip features two distinct culture chambers, allowing co-culture of various cell types within two separate compartments divided by a permeable membrane.

The Fluidic 480 is available in different configurations: chip materials (Topas (COC) or PS), optional surface treatment (none or hydrophilized), and multiple membrane pore size/color options (0.2 µm transparent or white, 0.4 µm, 3 µm transparent or translucent, and 8 µm; transparent if not specified). Mini Luer inlets and outlets provide leak-free connections and enable experiments under dynamic flow conditions.

General

This Organ-on-a-Chip with a cross-flow membrane allows you to reliably mimic physiological conditions in vitro and study tissue organization, cell-cell interactions, barrier penetration, and physiological responses in a more in vivo-like environment.

Two different and independent culture chambers are available on the same chip. This allows you to perform two experiments in parallel or in series (body-on-a-chip).

The two chambers are designed to develop models of physiological barriers and to ensure an in vivo-like environment under static or dynamic flow conditions. Each chamber indeed has 2 flow inlets and 2 outlets for the perfusion of culture media and testing solutions in both the apical and basolateral compartments.

The chip body is available in Topas (COC) or PS. Topas (COC) is optically clear and helps overcome common limitations of standard PDMS, with low unspecific absorption and excellent suitability for bright field and fluorescence microscopy. PS provides an alternative material option depending on your experimental needs.

The chip can be supplied untreated or hydrophilized to match wetting requirements and simplify handling for aqueous workflows.

The chip is equipped with a porous PET membrane and is available with several pore size/color options: 0.2 µm (transparent or white), 0.4 µm, 3 µm (transparent or translucent), or 8 µm (transparent if not specified).

Features

• Mini Luer connection molded with the chip: leak-free
• Standard microscope glass slide size (75.5 mm x 25.5 mm x 1.5 mm)
• Cover lid thickness: 140 µm
• 2 independent cell culture chambers
• Chip material options: Topas (COC) or PS
• Surface treatment options: none or hydrophilized
• Porous PET membrane options: 0.2, 0.4, 3, or 8 µm 

Cross-flow porous membrane	Upper/Apical compartment	Bottom/Basolateral compartment

Applications and examples from published papers

The upper and the lower compartments are separated by the porous membrane, and they can be perfused with different culture media. A tissue interface can be created to mimic alveolar, stomach, intestine, kidney, liver, brain-blood, skin functions, etc. Tissues inside the chip can be easily observed by microscopy.

Cell culture is just one potential application area of this versatile chip. The design indeed allows other different experiments such as small molecule transfer measurements, on-chip dialysis, and many more.

Intestine-on-chip

Maurer M. et al., A three-dimensional immunocompetent intestine-on-chip model as in vitro platform for functional and microbial interaction studies, Biomaterials 2019 (Download)

3D microphysiological model of the human intestine.

In this work, the model displays the physiological immune tolerance of the intestinal lumen to microbial-associated molecular patterns and can, therefore, be colonized with living microorganisms. The authors demonstrate that microbial interactions can be efficiently investigated using this chip creating a more physiological and immunocompetent microenvironment.

Endothelial Barrier-on-chip

Raasch M. et al., Microfluidically supported biochip design for culture of endothelial cell layers with improved perfusion conditions, Biofabrication 2015, 7: 015013 (Download)

The authors investigated cell viability, expression of endothelial markers, and cell adhesion molecules of ECs dynamically cultured under low and high shear stress. This chip allows an effective supply with nutrition medium, discharge of catabolic cell metabolites, and defined application of shear stress to ECs under laminar flow conditions.

They show that ECs cultured in the chip form a tight EC monolayer with increased cellular density and enhanced cell layer thickness compared to static and two-dimensionally perfused cell culture conditions. Endothelial layers in the chip express higher amounts of EC marker proteins von-Willebrand-factor and PECAM-1.

Liver-on-chip

Rennert K. et al., A microfluidically perfused three dimensional human liver model, Biomaterials 2015, 119-131 (Download)

The microfluidically perfused chip enables sufficient nutrition supply and resembles morphological aspects of the human liver sinusoid. It utilizes a suspended membrane as a cell substrate mimicking the space of Disse and the perfusion enhances the formation of hepatocyte microvilli. The authors stated that the perfused liver chip shares relevant morphological and functional characteristics with the human liver and represents a new in vitro research tool to study human hepatocellular physiology at the cellular level under conditions close to the physiological situation.

During culture in the biochip, HepaRG cells consistently differentiate into cells exhibiting a hepatocyte phenotype and into cells with a biliary epithelial cell phenotype that self-organize into a hepatocyte layer with functional bile ducts.

Content

1x Cross-flow membrane organ-on-a-chip with Mini Luer ports

Specifications

Please use this information to precisely define the key parameters of your cell seeding and experimental protocols. One chip allows you to perform two independent experiments.

Documentation

Click to read more information about ChipShop chips material properties.

General handling guide for cross-flow membrane chips (available soon)

Organ-on-a-chip cross-flow membrane chip Fluidic 480 datasheet

Maurer, M., Gresnigt, M. S., Last, A., Wollny, T., Berlinghof, F., Pospich, R., ... & Mosig, A. S. (2019). A three-dimensional immunocompetent intestine-on-chip model as in vitro platform for functional and microbial interaction studies. Biomaterials,220, 119396. https://doi.org/10.1016/j.biomaterials.2019.119396

Raasch, M., Rennert, K., Jahn, T., Peters, S., Henkel, T., Huber, O., ... & Mosig, A. (2015). Microfluidically supported biochip design for culture of endothelial cell layers with improved perfusion conditions. Biofabrication, 7(1), 015013. doi:10.1088/1758-5090/7/1/015013

Rennert, K., Steinborn, S., Gröger, M., Ungerböck, B., Jank, A. M., Ehgartner, J., Nietzsche, S., Dinger, J., Kiehntopf, M., Funke, H., Peters, F. T., Lupp, A., Gärtner, C., Mayr, T., Bauer, M., Huber, O., & Mosig, A. S. (2015). A microfluidically perfused three dimensional human liver model. Biomaterials, 71, 119–131. https://doi.org/10.1016/j.biomaterials.2015.08.043