Seplife® LXPM SP706M Polymeric Resin for Ion Exchange Chromatography

Synthetic Chromatography Resins

Appearance: White to light yellow spherical beads
Type: Strong acid cation - Sulfopropyl
Matrix: Polymethyl methacrylate
Ion exchange capacity (mmol/ml): 0.05-0.08
pH ligand fully charged: Negatively Charged at pH>2.5
Particle size range (micron): 50-100
Typical pore size (Å): 1000
pH stability: 3-12 (operational), 3-14 (CIP)
Chemical Stability: All commonly used aqueous buffers: 1 M NaOH, 0.1 M acetic acid, 8 M urea, 70% ethanol, 6 M guanidine hydrochloride, 2% benzyl alcohol
Flow rate* (cm/h): 500-600
10% Dynamic binding capacity (mg/ml)**: ≥55
Shipped as: Slurry in 20% ethanol solution containing 0.2M sodium acetate

*Testing conditions: Column size: 26x200mm, 0.3MPa, water
** Report testing conditions: Sample: lysozyme, Mobile phase: NaAc-HAc, pH 5.0, Column size: 8x100mm

Column packing
The best column packing results are obtained with the resin slurry in 0.5M NaCl at a concentration of 60%-70%.
· Mix the resins to form a homogenate and measure the desired mass or volume, about 1.2 times the column volume.
· Replace 20% ethanol with 0.5 M NaCl solution and equilibrate overnight.
· Before loading the column, adjust the slurry concentration to 65-70% with 0.5 M NaCl solution; pour the resin slurry into the chromatography column in one go, allow to sediment by gravity and mark the bed height after sedimentation.
· Load the distributor and adjust the height so that the compression coefficient is 1.05-1.10; then pump 0.5M NaCl through the column and stabilize the bed with 1.5 to 2 times the highest working flow rate. (2 - 5 bed volumes (BV).
· Efficiency and asymmetry determinations can be performed as described below.

Column Efficiency Evaluation
The test method for column efficiency of the chromatography columns is as follows:
Mobile phase: 0.5 M NaCl solution
Linear flow rate: 100 cm/h
Sample: 2 M NaCl solution
Loading volume: 0.5-1% of column volume
Detection: Conductivity detector
Acceptable column asymmetry factor is in the range 0.8-1.8.

Rinsing
The loaded columns should be rinsed with at least 5 BV of deionized water.

Equilibration
Equilibrate the column with an appropriate 5-10 column volume buffer until the conductivity and pH of the effluent remain unchanged. The specific buffer system should be screened and optimized according to the stability and isoelectric point of the target protein and the type of ion exchange medium.

Sample feeding
The solid sample can be prepared by dissolving in the equilibrium solution; the low concentration sample solution can be dialyzed in the equilibrium buffer; the high concentration sample solution can be diluted with the equilibrium solution. To avoid clogging of the column, samples should be processed by centrifugation or membrane filtration. The feed amount is calculated according to the capacity of the resin and the content of the target protein in the feed solution. Before loading, ensure that the sample buffer is as consistent as possible with the equilibration solution.

Elution
After loading the sample, continue rinsing with equilibration buffer until the baseline is stable. Typically, the molecules retained on IEX chromatographic media are eluted by increasing the salt concentration or changing the pH to ensure repulsion of the charged species.

Regeneration
After each chromatography cycle, the media can be regenerated with 0.5-2 M NaCl to remove the strongly bound protein.

Cleaning-in-place (CIP)
In order to maintain the performance of the chromatographic column, if there are proteins or other impurities that cannot be effectively removed during the regeneration process, a CIP step should be performed. Up-flow CIP may increase the efficiency of the process. The recommended operation steps are as follows:
1) For precipitated, hydrophobically bound proteins or lipoproteins, wash with 0.2-0.5 M NaOH (contact time 1-2 h), followed by rinsing with equilibration solution (approx. 5 BV) and deionized water (approx. 3 BV);
2) For proteins retained by hydrophobic bonds, lipoproteins and lipids, wash with 50% ethanol or 30% isopropanol (approx. 5 BV, contact time 0.5-1 h), and rinse with deionized water (approx. 5 BV).
3) Other options: media can be cleaned with alkaline or acidic solutions containing non-ionic surfactants, such as 0.1-0.5% Triton X-100 in 0.1 M acetic acid for 1-2 h, and rinse with 50% ethanol (approx. 5 BV). To remove the detergent, rinse with water (approx. 5 BV). When using high-concentration organic solvents, it is recommended to gradually increase the solvent concentration in the mobile phase in order to avoid bubbling.

Storage
Chromatography resins that are not for immediate use should be stored in 20% ethanol at 4-30 °C. The loaded column should be stored in a buffer containing 20% ethanol (pH 7.0). Clean the ethanol after packing the column and before use.