Scalable crossflow separation technology

Tangential Flow Filtration

Scalable hollow-fiber and cassette solutions for microfiltration, ultrafiltration and diafiltration.

Nominal pore size or MWCO alone does not guarantee process performance

Tangential flow filtration product family
Scalable crossflow filtration portfolio Hollow fiber · Cassette · MF / UF / DF
2 formats Hollow fiber and cassette
0.1–0.65 µm Microfiltration ratings
1–1000 kDa Ultrafiltration MWCO range
28 cm²–16.8 m² Portfolio membrane area

Configure crossflow separation from cell retention to macromolecule concentration and buffer exchange.

Tangential flow moves process fluid parallel to the membrane while pressure drives smaller components into the permeate. Retained cells, particles or macromolecules remain in the retentate stream for recirculation, concentration or diafiltration.

Format 01 · Hollow-fiber MF

Open flow paths for clarification and cell retention

Modified-PES hollow fibers provide smooth tubular flow paths for cell- or particle-containing feeds, selected perfusion duties and clarification applications.

  • 0.1, 0.2, 0.45 and 0.65 µm ratings
  • Areas from 28 cm² to 16.8 m²
  • Process scale from 300 mL to 1500 L

Separation regime Microfiltration

Format 02 · Hollow-fiber UF

Gentle concentration and diafiltration

Modified-PES hollow-fiber ultrafilters combine relatively low hold-up volume with open flow paths for shear-sensitive products and compatible biological assemblies.

  • 50, 100, 300, 500 and 750 kDa MWCO
  • Areas from 28 cm² to 16.8 m²
  • Small-scale tubing and sanitary interfaces

Separation regime Ultrafiltration / diafiltration

Format 03 · Cassette UF

Flat-sheet modules with selectable channel geometry

Regenerated-cellulose and PES cassettes provide broad MWCO choice with tight, coarse, high-viscosity, suspended/open and custom channels.

  • 1 to 1000 kDa MWCO range
  • Areas from 100 cm² to 0.5 m²
  • Development through production processing

Channel options Tight to open / custom

Separation rating and flow-path selection

Select the membrane and channel for the intended retentate, permeate and concentration range.

Micrometer pore ratings and molecular-weight cutoffs describe different separation regimes. Membrane chemistry, effective target size, feed solids, viscosity, crossflow, transmembrane pressure and concentration polarization all influence observed retention and flux.

Parallel flow Crossflow sweeps the membrane surface
Retentate / permeate Define where the target product must report
01 Hollow-fiber MF · 0.1–0.65 µm Clarification, cell or particle retention and passage of smaller soluble components Cell / particle scale
02 Hollow-fiber UF · 50–750 kDa Concentration and diafiltration of selected macromolecules, particles or biological assemblies Gentle UF / DF
03 Cassette UF · 1–1000 kDa Broad MWCO selection for retaining targets while smaller impurities and buffer components permeate Broad MWCO choice

Crossflow processing for clarification, concentration and buffer exchange.

Performance depends on feed composition, viscosity, crossflow, transmembrane pressure, temperature, process time, hold-up volume and channel geometry. Representative trials are required before scale-up.

01

Harvest clarification and cell retention

Cell-culture and fermentation clarification, cell retention and selected perfusion-process operations.

02

Protein and peptide concentration

Concentration of monoclonal antibodies, recombinant proteins, enzymes and peptides.

03

Vaccines and viral vectors

Concentration and purification support for compatible vaccines, viral vectors and biological assemblies.

04

Nucleic acids and macromolecules

Concentration of nucleic acids and other compatible high-molecular-weight products.

05

Diafiltration and buffer exchange

Desalting, buffer exchange and removal of low-molecular-weight impurities from retained products.

06

Volume reduction and scale-up

Volume reduction before chromatography or formulation, from laboratory screening through manufacturing.

Establish flux and retention across the full concentration range.

Screen candidate membranes and channels with representative feed, then scale using normalized membrane area, crossflow, transmembrane pressure, system geometry and an appropriate process safety factor.

01

Separation objective

Define microfiltration, ultrafiltration, concentration or diafiltration duty and whether the target stays in retentate or permeate.

02

Target and feed profile

Provide molecular or particle size, aggregation state, solids, turbidity, viscosity and concentration profile.

03

Membrane and channel geometry

Select membrane chemistry, pore rating or MWCO, hollow-fiber lumen or cassette screen for the expected feed behavior.

04

Hydrodynamic conditions

Establish crossflow, shear sensitivity, channel pressure drop, transmembrane pressure and flux targets.

05

Volume and recovery

Confirm starting and final volume, concentration factor, diafiltration volume, hold-up volume and recovery target.

06

System and lifecycle strategy

Define membrane area, process time, connections, holder, tubing, pump, instrumentation and single-use or reusable approach.

Configuration matrix

Review membrane media, ratings, areas, process scales and interfaces.

Offered combinations are format dependent. Hollow-fiber modules use integral module connections, while cassette devices require a compatible holder and manifold. Confirm product binding, compatibility, cleaning or sanitization exposure, extractables and recovery with the actual process fluid.

Media selection Module configuration

Media options

Media General characteristics Suggested applications
Modified PES Hydrophilic polyethersulfone membrane offering high flow, mechanical strength and broad use across microfiltration and ultrafiltration Hollow-fiber MF and UF; selected cassette concentration and diafiltration applications
Regenerated cellulose Hydrophilic membrane with low nonspecific protein interaction and strong product-recovery potential Cassette ultrafiltration of protein-sensitive streams, concentration and buffer exchange

Product configurations

Format / channel Media Nominal rating Filtration area Process scale Interface
Hollow-fiber microfiltration Modified PES 0.1 / 0.2 / 0.45 / 0.65 µm 28 / 56 / 118 / 236 / 471 cm²; 0.15–16.8 m² 300 mL–4 L; 6–1500 L Female/male Luer; 3/8 in. hose barb; 1/2, 1-1/2 and 2 in. sanitary clamp
Hollow-fiber ultrafiltration Modified PES 50 / 100 / 300 / 500 / 750 kDa 28 / 56 / 118 / 236 / 471 cm²; 0.15–16.8 m² 300 mL–4 L; 6–1500 L Female/male Luer; 3/8 in. hose barb; 1/2, 1-1/2 and 2 in. sanitary clamp
Cassette · Tight screen RC / PES 1 / 3 / 5 / 8 / 10 / 30 / 50 / 100 / 300 / 500 / 1000 kDa 100 cm² 200–2000 mL Compatible holder / manifold
Cassette · Coarse screen RC / PES 1 / 3 / 5 / 8 / 10 / 30 / 50 / 100 / 300 / 500 / 1000 kDa 200 cm² 200–2000 mL Compatible holder / manifold
Cassette · Open / high-viscosity screen RC / PES 1 / 3 / 5 / 8 / 10 / 30 / 50 / 100 / 300 / 500 / 1000 kDa 0.11 m² 5–50 L Compatible holder / manifold
Cassette · Suspended / open channel RC / PES 1 / 3 / 5 / 8 / 10 / 30 / 50 / 100 / 300 / 500 / 1000 kDa 0.46 m² ≥50 L Compatible holder / manifold
Cassette · Custom screen RC / PES 1 / 3 / 5 / 8 / 10 / 30 / 50 / 100 / 300 / 500 / 1000 kDa 0.5 m² Not specified Compatible holder / manifold

Prepare the right TFF configuration for your customer project.

Confirm the separation objective, target location, representative feed, membrane, rating, channel, crossflow, transmembrane pressure, starting and final volumes, recovery, membrane area, system interfaces and lifecycle strategy before submitting the final RFQ for technical review.