Ultrafiltration (UF) is a pressure-driven filtration process that utilizes a semipermeable membrane with pore sizes ranging from 0.01 to 0.1 µm. The pore size defines the nominal molecular weight cutoff (MWCO) of a membrane, specifying the minimum molecular weight of the particle effectively retained by a membrane.
UF is effectively used for sample concentration, diafiltration (buffer exchange, desalting), and size fractionation. These processes are integral to any preparative scale purification workflows involving macromolecules to maintain them at appropriate concentrations and in a suitable buffer for optimal functioning.
Modes of Ultrafiltration
There are two fundamental modes of ultrafiltration:
Dead-End Filtration
In dead-end filtration (DEF), the feed flows perpendicular to the membrane surface and the pressure for filtration is generated by centrifugal force. The dead-end devices only have a feed and permeate stream, while the retentate is not recirculated. This allows the entire feed stream to be pushed through the membrane and the small molecules are collected at the permeate side.
Dead-End Filtration
The simplicity of this mode makes it a popular choice for small-scale operations and laboratory studies. However, ultrafiltration using dead-end devices is limited by low filtration rates due to filter cake formation and lack of scalability. Because it is a hands-on method, it is often accompanied by sample loss. Additionally, these devices/membranes can be difficult to clean due to the extensive plugging of the narrow fibers/channels.
Tangential-Flow Filtration
The tangential-flow filtration (TFF) has the crossflow geometry in which the feed stream is pumped parallel to the membrane surface and perpendicular to the filtrate. Unlike DEF, TFF requires three distinct process streams: the feed, the permeate, and the retentate. In order to obtain high rates of mass transfer, it is necessary to have high tangential velocity and/or turbulence in the immediate vicinity of the membrane. This tangential velocity and turbulence help to prevent filter cake formation on the membrane and eventually avoid the decline in flux rate.
Tangential-Flow Filtration
The basic components of a conventional TFF include a reservoir, a pump, the membrane, the tubes that connect these components, and the pressure gauges. The pressure gauges, feed pressure, and return pressure present before and after the membrane, respectively, regulate the filtration rate by creating transmembrane pressure (TMP), which drives the small molecules through the membrane pores.
TFF Modules
Hollow Fiber
This module utilizes numerous hollow, narrow-diameter (0.1-2 mm) membrane tubes in the form of bundles. Feed is pumped inside the tubes, and the small molecules permeate through the walls of the tubes. This open path minimizes shear stress due to moderate cross-flow rates making it ideal for the processing of shear-sensitive products. However, hollow fibers have low efficiency as they require high pumping capacity to achieve high flux rates.
Hollow Fiber
Spiral Wound
Spiral Wound
Spiral wound modules consist of alternating membrane and separator layers wrapped around a central core. Feed is pumped axially through the cartridge, while filtrate permeates the membrane and radially spirals towards the core. Separator screens enhance turbulence, boosting efficiency as compared to hollow fibers. The main drawback to spiral wound modules is that they are not linearly scalable because either the feed flow path length (cartridge length) or the filtrate flow path length (cartridge width) must be changed within scales. Despite this, their low cost and high membrane surface area make them excellent choices for large-scale food and beverage applications.
Flat Plate
Flat plate membrane module consists of single or stacked layers of membranes, potentially interspersed with separator screens, enclosed in a sealed unit. This module offers high membrane packing density, resulting in a significant membrane surface area per unit footprint. The feed solution, applied to one side of the membrane, traverses through the channels, and the permeate is collected from the other side. The flat plate module is a better option for shear-sensitive feeds and offers high flow rates as well as ease of cleaning.
Flat Plate
Overall, the TFF effectively addresses the limitations associated with DEF such as lack of scalability, low filtration rate, aggregation and sample loss. However, the conventional TFF systems are bulky and have longer fluid paths, resulting in high hold-up volumes, making them unsuitable for lab scale applications. Therefore, an automated TFF system with a small footprint and minimal hold-up volume is well suited for laboratory research and experimentation.
The µPulse: An Automated and Miniaturized TFF System
The µPulse is an automated and miniaturized TFF system designed explicitly for lab scale applications. The entire fluid path is miniaturized on a filter chip that has been designed by combining the TFF with microfluidic pumping technology. This has drastically reduced the hold-up volume to 0.65 mL, making it well suited for lab scale applications. The filter chips can be cleaned in place for re-use up to 300 mL of permeate and are available with modified polyethersulfone (mPES) and regenerated cellulose (RC) membranes in a range of MWCOs (5 - 300 kDa). The table below provides information about the selection of MWCO membrane to process various biomolecules. Compared to dead-end centrifugal units, the µPulse offers up to 4x higher filtration rates. While the dead-end centrifugal units require manual intervention, the weight-based volume sensing in µPulse ensures effective control on final volume, enabling single step and walk-away sample processing.
| Membrane MWCO (kDa) | Molecular/Particle Size (nm) | Protein (kDa) | Double Stranded Nucleic Acid (bp) | Single Stranded Nucleic Acid (bs) |
|---|---|---|---|---|
| 5 | 3-5 | 15-30 | 25-50 | 50-95 |
| 10 | 5-9 | 30-90 | 50-145 | 90-285 |
| 30 | 9-15 | 90-180 | 145-285 | 285-570 |
| 50 | 15-30 | 150-300 | 240-475 | 475-950 |
| 100 | 30-90 | 300-900 | 475-1450 | 950-2900 |
| 300 | 90-200 | 900-1800 | 1450-2900 | 2900-5700 |
Table: Membrane MWCO selection for various biomolecules
The µPulse is Designed for a Broad Range of Scientific Workflows
Nanoparticle Processing
Efficiently process lipid nanoparticles, liposomes, and polymeric nanoparticles for drug delivery and therapeutic efficacy
Protein Processing
Optimize the protein preparative workflow, enabling fast and gentle processes, including concentration, formulation, desalting, and refolding
Bioconjugate Cleanup
Ensure gentle and efficient removal of small unconjugated molecules from a variety of crude biomolecular labeling reactions
Nucleic Acid Processing
Simplify in vitro synthesis of RNA, and linear or plasmid DNA, by efficient concentration and buffer exchange using our user-friendly system
Harvesting
Streamline the fast harvesting of cells, cell lysates, extracellular vesicles (EVs), and secretory products while ensuring high product yields and quality
Virus Processing
Gently concentrate and buffer exchange Adeno-Associated Virus Vectors (AAVs), bacteriophages, Virus Like Particles (VLPs) and lentiviruses, preserving their structure for effective applications
Vaccine Development
Empower the formulation of DNA, RNA, and polysaccharide vaccines for optimal results
Webinars
Uncover the ease of use, scalability, and reusability of µPulse for lab-scale formulation of recombinant L-asparaginase and other biomolecules.
Discover how the nanoparticles are processed in a fast, single step and walk-away manner with the µPulse TFF system.
Experience the single-step and scalable purification of ADCs and other macromolecules modified with small molecules using the µPulse.
Explore the ease of use, and cost-effectiveness of µPulse for processing VLPs and other macromolecules compared to dead-end units.
Application Notes
Learn about the time efficiency, cost effectiveness and gentleness of µPulse for refolding denatured proteins compared to equilibrium dialysis.
Explore the efficiency, fast processing, and gentleness of the miniaturized µPulse TFF system for concentration and buffer exchange of protein samples.
Publications
Secretome of Hypoxia-Preconditioned Mesenchymal Stem Cells Ameliorates Hyperglycemia in Type 2 Diabetes Mellitus Rats
Widyaningsih et al., 2024 | Trends in Sciences | Link: https://doi.org/10.48048/tis.2024.7278
Introduction: Type 2 diabetes mellitus (T2DM) is a prevalent form of diabetes that affects 90 - 95 % of all diabetic patients. Insulin sensitizers and insulin exogenous supply could temporarily ameliorate hyperglycaemia; however, they are accompanied by side effects. As a result, new approaches are required to address insulin resistance and regenerate beta cells simultaneously. The secretome of hypoxic mesenchymal stem cells More.... | Related Solution: µPulse TFF System
Combination Effect of Rotator Cuff Repair with Secretome-hypoxia MSCs Ameliorates TNMD, RUNX2, and Healing Histology Score in Rotator Cuff Tear Rats
In order to treat a rat model of rotator cuff rupture, this work concentrated on the expression of TNMD and RUNX2, followed by rotator cuff repair and secretome-hMSCs. Methods: A total of thirty 10-weeks-old male Sprague–Dawley rats were separated into five groups randomly, RC on week 0, lesion treated with a rotator cuff repair and saline (RC + NaCl group, n = 6) for 2 and 8 weeks, and lesion treated with a rotator cuff repair and More.... | Related Solution: µPulse TFF System
The Role of Mesenchymal Stem Cell Secretome in the Inflammatory Mediators and the Survival Rate of Rat Model of Sepsis
Sari et al., 2023 | Biomedicines | Link: https://doi.org/10.3390/biomedicines11082325
In sepsis, simultaneously elevated levels of pro-inflammatory cytokines and interleukin (IL)-10 indicate immune response dysregulation, increasing the mortality of the host. As mesenchymal stem cell (MSC) secretome is known to have immunomodulatory effects, we aim to assess the role of MSC secretome in the inflammatory mediators (NF-κB p65 and p50, TNF-α, IL-10) and the survival rate of a rat model of sepsis. In this study, forty-eight male More.... | Related Solution: µPulse TFF System
Structural and functional analyses of Pcal_0917, an α-glucosidase from hyperthermophilic archaeon Pyrobaculum calidifontis
Genome analysis of Pyrobaculum calidifontis revealed the presence of α-glucosidase (Pcal_0917) gene. Structural analysis affirmed the presence of signature sequences of Type II α-glucosidases in Pcal_0917. We have heterologously expressed the gene and produced recombinant Pcal_0917 in Escherichia coli. Biochemical characteristics of the recombinant enzyme resembled to that of Type I α-glucosidases, instead of Type II. More... | Related Solution: µPulse TFF System