Perfuse 3D biology: organoids, spheroids, and 3D tissues.
The PerFuseIt manifold is customizable to different well plate sizes and can provide continuous media circulation of static cultures. The system can also integrate with transwell inserts to incorporate a flow-through collection and analysis strategy for your assays.
Perfuse 3D Cell and Tissue Cultures
3D bioprint cells
into well plate
cassette and pumps
Perfuse and incubate
3D model in-vitro
Drip & Sip.
Drips media into single wells and sips it out. Ideal for organoids and spheroids. Inlet drips media into a well and outlet sips from the top of the collected media within the well, maintaining a particular fluid volume. Input/output heights and spatial locations of the well are customizable.
Perfuse into basket and out of membrane. Ideal for cell interaction studies. Inlet drips media into transwell basket and media flows through cell/tissue culture and porous transwell mesh into the well below. The outlet sips from the top of the collected media to maintain a specific fluid height. Transwell provides hydrostatic pressure-driven flow through 3D tissue or cell culture.
Better Tissue Conditioning.
Flow-based conditioning of engineered tissues.
More Viable Biology.
Enable better cell & tissue viability, function and longevity with cell nourishment.
Create in-vitro perfusable organ models easily to study microphysiological environments and test reactions.
Easier Angiogenesis Assays.
Direct vascular self-assembly with nourished stromal cells.
PerFuseIt Key Features & Specifications:
Integrates with Standard Syringe Pumps
Perfuse bioprinted constructs, organoids, and spheroids
Compatible with all culture medias and reagents
Integrates directly into your workflow
Manifold Configurations Available:
6, 12, 24, 48, or 96-well plates
Compatible Well Plates:
Corning Costar 6, 12, 24, 48,
or 96-well plates
Any single or multi-channel
0.0625” outer diameter,
0.03” inner diameter FEP tubing
Ready to bring PerFuseIt to your lab?
Book a demo or get a quote:
The Advanced Solutions Louisville, KY facility has been audited by UL Registrar LLC and meets GMP requirements listed in RCP, NBCP, or Pharmaceutical Certification Schemes which is uniquely accredited by the American National Standard Institute (ANSI) developed in accordance with applicable sections of the FDA’s code of federal regulations.