Introduction to Concentration and Buffer Exchange using Amicon® Stirred Cells

Request Information

---

Sample preparation of macromolecule solutions, such as proteins, enzymes, antibodies, and viruses, often yield large volumes of diluted macrosolutes in buffers that are incompatible with downstream processes or detection.

Centrifugal ultrafiltration devices (such as the Amicon® Ultra Filters) are regularly used to concentrate and buffer-exchange these types of macrosolutes; however, volumes larger than 50 mL present significant challenges, requiring samples to be loaded in multiple stages or aliquoted over several devices.

The Amicon® Stirred Cell family of pressure-driven filtration devices provide an ideal solution for concentrating and buffer-exchanging large volumes of macrosolutes. These devices are available in multiple sizes to offer a wide range of processing volumes. To process even larger volumes, an external reservoir can be attached to any Amicon® Stirred Cell.

The new generation of Amicon® Stirred Cells provides ergonomic benefits, integrated safety features, a more secure stir bar, superior integrity, and ease of use while also providing a broader selection of membrane discs.

Simultaneous Sample Concentration and Buffer Exchange by Ultrafiltration Plus Diafiltration

Ultrafiltration is a proven method for sample concentration. When combined with diafiltration, the analyte of interest is provided at a concentration and in a buffer that is compatible with additional purification and analysis steps. During ultrafiltration, the desired macrosolute concentration is achieved because the concentration of non-permeating species is increased while the fluid volume is reduced. Furthermore, the concentration of membrane-permeating species such as salts and microsolutes remains unchanged.

How to Choose the Correct Ultrafiltration Membrane (NMWCO) for the Sample

When using ultrafiltration for sample concentration, particular attention has to be paid in choosing the correct membrane molecular weight cut-off, as well as membrane material. Ultrafiltration membranes are typically made from regenerated cellulose or polyethersulfone (PES). The material of choice will greatly depend on sample compatibility. The choice of membrane nominal molecular weight cut-off (NMWCO) will depend on the molecular weight (MW) of the macrosolute that is to be retained. Membrane choice will have a significant impact on performance. As a rule, the NMWCO should be 2-3 times smaller than the molecular weight of the solute to be retained when using regenerated cellulose and 4-5 times smaller for Biomax® PES membranes.

Solute retention may be further influenced by:

• Processing temperature
• Operating pressure
• Stir speed
• Sample concentration 
• Sample constitution

You may need to optimize the above parameters to assure desired yield. The most frequently used ultrafiltration membranes have a NMWCO range of 3 kDa to 100 kDa, although smaller and larger pore sizes are available.

Diafiltration Compared to Dialysis

Diafiltration is a technique that uses ultrafiltration for buffer exchange. Diafiltration can rapidly and efficiently eliminate salts and/or microsolutes from macromolecular mixtures. This process is typically called “washing out.”

The term “washing in” is used when diafiltration is employed to replace one salt species or microsolute with another, as is done during buffer exchange.

Traditional dialysis is an alternative buffer exchange technique; however, it has several drawbacks: In contrast, diafiltration uses ultrafiltration membranes, either in centrifugal or pressure-driven devices such as the Amicon® Stirred Cell, for efficient buffer exchange.

Advantages of diafiltration using stirred cell ultrafiltration:

Diafiltration	Dialysis
Transport convective with solvents, independent of microsolute composition	Transport diffusion-controlled, dependent on type of microsolute
Smaller volume of exchange buffer required	High volume of exchange buffer volume required, efficient mixing and frequent buffer changes required to drive efficient transport
Rapid exchange rate. Fractional removal of solvent microsolute is independent of sample composition	Exchange rate is slow and efficiency is reduced with decrease microsolute concentration
Ultrafiltration rate reduced with decreased temperature	Reduced microsolute transport with decreased temperature
At high macrosolute content, ultrafiltration rate and microsolute transport are reduced	Microsolute transport unaffected by content of retained Macrosolutes
Scalable; compatible with samples ranging from few microliters to many liters	Not easily scalable to large volume, best used for microliter-to-liter volume samples.

Continuous vs. Discontinuous Diafiltration

Diafiltration can be performed in either continuous or discontinuous mode. Discontinuous diafiltration refers to a practice where the sample is first concentrated, then diluted with exchange buffer to the initial starting volume, followed by another concentration step. This process is repeated until the desired microsolute has been exchanged.

On the other hand, continuous diafiltration maintains a constant volume throughout the buffer exchange process, by introducing exchange buffer at the same rate as filtrate is being removed. By maintaining a fixed volume, the retained solute concentration remains constant, providing a gentler method of buffer exchange.

In general, continuous diafiltration is more efficient than discontinuous diafiltration. In discontinuous diafiltration, the permeate flux decreases as the sample concentration increases, which can contribute to membrane fouling and cause increased retention of microsolutes that would otherwise pass through the membrane.

---

Calculating Buffer Exchange Volume for Continuous Diafiltration

Buffer Requirements for Continuous Diafiltration

---

Calculating Buffer Exchange Volume for Discontinuous Diafiltration