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Ion Exchange Chromatography Media
Ion Exchange Chromatography Media
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United Kingdom
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AMSBIO
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AMSBIO
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1110 
Updated:
8/9/2018
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    Ion Exchange Chromatography Media
    Cellufine MAX S, Q, CM, DEAE

     

    High Flow Rate, High Binding Capacity

    Cellufine MAX is the new, high-flow, Cellufine media. Advanced cross-linking technologies have created more robust base beads operable at high flow and pressure. Further, Cellufine MAX ion exchange (IEX) media are made using surface modification techniques that dramatically increase ligand availability, which translates to higher dynamic binding capacities. Cellufine MAX IEX media are offered in six products, including both anion and cation chemistries.

     


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    Cellufine MAX Base Resin
    Cellulose, natural polysaccharide, possesses unique crystalline molecular structure differing from non-crystalline polysaccharides such as agarose. Thus Cellufine has unique pore structure as shown in the pictograph (Fig. 1). The new Cellufine MAX series offers the largest pore size of all Cellufine chromatography media. The benefit of such pore size in Cellufine MAX IEX media provides superior strength and excellent mass transfer. This is seen in the break-through curves for thyroglobulin, a very large protein (Fig. 2).
     
    SEM analysis of Cellufine MAX base resin
    Fig 1. SEM analysis of Cellufine MAX base resin
    Typical break-through curves for Cellufine. DEAE weak anion exchange media with thyroglobulin
    Fig 2. Typical break-through curves for Cellufine 
    DEAE weak anion exchange media with thyroglobulin
     
     
    Partial Structure of Cellufine MAX IEX Media

    Ligand structure for Cellufine MAX IEX media are described in Fig. 3. S, Q, CM and DEAE are correspondingly strong cation, strong anion, weak cation and weak anion exchangers. Two sub-types, h and r, are available for Cellufine MAX S and Q.
    The differences between X-h and X-r type Cellufine MAX strong ion exchange media (X) are due to the design of the media. The X-h type is designed for higher binding capacity than the X-r type by optimizing the ligand content and dextran scaffold.
      Ligand structure of Cellufine MAX IEX
    Fig 3. Ligand structure of Cellufine MAX IEX

     

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    Characteristics of Cellufine MAX IEX Media
    The basic characteristics of Cellufine MAX IEX media are shown in Table 1. All Cellufine MAX IEX media are based on 90 μm (average) highly cross-linked cellulose beads, which are surface-modified with dextran. Cellufine MAX IEX media are designed for use in bio-pharmaceuticals purification processes.
    Characteristics
    Type MAX CM MAX S-r MAX S-h MAX DEAE MAX Q-r MAX Q-h
    Matrix Cross-linked cellulose with dextran scaffold
    Particle size (μm) 40 -130
    Ligand CM S S DEAE Q Q
    Ion exchange capacity (meq / ml-gel) 0.09 - 0.22 0.12 - 0.24 0.13 - 0.25 0.14 - 0.25 0.13 - 0.20 0.17 - 0.24
    10% DBC(mg/ml) Lysozyme 220 144 191      
    BSA       197 141 225
    human-γ-globulin 104 131 216 108 74 135
    pH stability 2 -13 2 -13 3 -14 2 - 12 2 - 12 2 - 12
    Storage 20% Ethanol
       
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    Pressure-flow Properties of Cellufine MAX IEX Media
    Cellufine MAX IEX media enable high-flow operation, which is essential to efficient purification of bio-pharmaceuticals. The figures below show pressure-flow velocity curves of Cellufine MAX IEX media in a 30 cm column with a 20 cm bed height (Fig. 4). All Cellufine MAX IEX media are operable at practical flow velocities (500 cm/h) and pressures.
     
    Cellufine MAX Cation Exchange MediaCellufine MAX cation exchange media   Cellufine MAX Anion Exchange MediaCellufine MAX anion exchange media  
     
    Fig 4. Pressure-flow velocity curves for Cellufine MAX IEX exchange media 
    Column: 30 cm I.D. x 20 cm L 
    Mobile phase: Pure Water at 24 ºC
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    Dynamic Binding Capacities of Cellufine MAX IEX Media
    Efficient mass-transfer characteristics of Cellufine MAX IEX media translate to superior dynamic binding capacities (DBC). Figure 5 to 7 show DBC of model proteins at different residence times for Cellufine MAX IEX media. All Cellufine MAX IEX media are stable over a range of residence times. 
    Fig. 8 shows that Cellufine MAX S exhibits superior dynamic binding performance across a range of protein characteristics to competitive media. 
    These unique characteristics of Cellufine MAX IEX media make it suitable for use in up-stream as well as to down-stream steps in bio-pharmaceuticals purification.
    Cellufine MAX Cation Exchange MediaCellufine MAX cation exchange media: Resistance times   Cellufine MAX Anion Exchange Media
    Cellufine MAX anion exchange media
     
    Fig. 5 Residence time vs. IgG-DBC for Cellufine MAX S
    Column:5 mm ID×50 mm L
    Sample:human polyclonal IgG (1 mg/ml)
    Buffer:10 mM Acetate-50 mM NaCl (pH 4.3)
       
    Fig 6. Residence time vs. BSA-DBC fer Cellufine MAX Q 
    Column: 5 mm I.D. x 100 mm L 
    Sample: BSA (1 mg/ml)
    Buffer:50 mM Tris-HCl (pH 8.5)

     

    Cellufine MAX Weak ion Exchange Media
    Cellufine MAX weak ion exchange media
      Cellufine MAX Cation Exchange Media
    Cellufine MAX cation exchange media: IgG, BSA, Lysozyme
    Fig. 7 Residence time vs. DBC for Cellufine MAX CM (polyclonal IgG) and DEAE (BSA)
    Column:5 mm ID x 50 mm L
    Sample:human polyclonal IgG (1 mg/ml)
    BSA (1 mg/ml)
    Buffer:10 mM Acetate (pH 5.6) for IgG
    Tris-HCl (pH 8.5) for BSA
     
    Fig. 8 DBC of Cellufine MAX S and agarose base media 
    with various model proteins (R.T. = 1 min)
    Polyclonal IgG:10 mM Acetate (pH 4.3) - 50 mM NaCl 
    BSA:10 mM Acetate (pH 4.3) - 50 mM NaCl 
    Lysozyme:Tris-HCl (pH 9.5)

     

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    Model Proteins Separation Performance for Cellufine MAX IEX Media
    Cellufine MAX IEX media are optimized for high adsorption and high resolution. Model protein separation with MAX S-h and MAX CM (Strong Cation vs. Weak Cation) is demonstrated in Fig. 9 and 10.
     
    Cellufine MAX Cation Exchange Media   Cellufine MAX Anion Exchange Media
    Cellufine MAX Anion exchange media: Transferrin, BSA, Pepsin
     
    Fig. 9 Model proteins separation for Cellufine MAX S-h and MAX CM
    Column:6.6 mm ID×50 mm L
    Buffer A:10 mM phosphate buffer (pH 7)
    Buffer B:10 mM phosphate (pH 7) + 1 M NaCl 
          (0→50 % linear gradient)
    Flow rate:0.86 ml/min (residence time: 2min)
    Proteins:Ribonuclease A (5 mg/ml), 
         Cytochrome C (2.5 mg/ml),
         Lysozyme (1.5 mg/ml)
    Injection volume:1.5ml
       
    Fig. 10 Model proteins separation for Cellufine MAX Q-h and MAX DEAE
    Column:6.6 mm ID×50 mm L
    Buffer A:50 mM Tris-HCl (pH 8.5)
    Buffer B:50 mM Tris-HCl (pH 8.5) - 1 M NaCl 
         (0→75 % linear gradient)
    Flow rate:0.86 ml/min (residence times 2 min)
    Proteins:Transferrin (5 mg/ml), 
         BSA (10 mg/ml),
         Pepsin (5 mg/ml)
    Injection volume:1.5 ml

     

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    Chemical Stability and Cleaning-In-Place
    Cellulose is well-known as a natural product having chemical and physical stability. Thus, since Cellufine is derived from cellulose, it also is stable to chemicals, caustic and acidic solutions. CIP of all Cellufine MAX IEX media can be carried out with 0.5 M NaOH solution. Used media should be stored in 20 % ethanol at 2 - 25 ºC after cleaning.

     

    Cellufine MAX S-r
    Quantity Buy Now
    1ml x 5 (Mini-Column) 20300-51
    5ml x 5 (Mini-Column) 20300-55
    100ml 20300
    500ml 20301
    5 lt 20302
    10 lt 20303
    pdf Operating Instructions
    pdf Technical data sheet
    pdf MAX Mini-columns
    Cellufine MAX S-h
    Quantity Buy Now
    1ml x 5 (Mini-Column) 20400-51
    5ml x 5 (Mini-Column) 20400-55
    100ml 20400
    500ml 20401
    5 lt 20402
    10 lt 20403

     

    Cellufine MAX Q-r
    Quantity Buy Now
    1ml x 5 (Mini-Column) 20500-51
    5ml x 5 (Mini-Column) 20500-55
    100ml 20500
    500ml 20501
    5 lt 20502
    10 lt 20503
    pdf Operating Instructions
    pdf Technical data sheet
    pdf MAX Mini-columns
    Cellufine MAX Q-h
    Quantity Buy Now
    1ml x 5 (Mini-Column) 20600-51
    5ml x 5 (Mini-Column) 20600-55
    100ml 20600
    500ml 20601
    5 lt 20602
    10 lt 20603

     

    Cellufine MAX CM
    Quantity Buy Now
    1ml x 5 (Mini-Column) 20900-51
    5ml x 5 (Mini-Column) 20900-55
    100ml 20900
    500ml 20901
    5 lt 20902
    10 lt 20903
    pdf Operating Instructions
    pdf Technical data sheet
    Cellufine MAX DEAE
    Quantity Buy Now
    1ml x 5 (Mini-Column) 21000-51
    5ml x 5 (Mini-Column) 21000-55
    100ml 21000
    500ml 21001
    5 lt 21002
    10 lt 21003
    pdf Operating Instructions
    pdf Technical data sheet



     

    View all Cellufine Chromatography Media Products

    bio-equip.cn
    AMSBIO’s mission is to be a profitable premier provider of quality life science research reagents and services helping customers develop innovative methods, processes, products and medicines. This is achieved by offering small and medium size manufacturers, academic groups and revenue generating biotechs a unique partnership for the global market and by providing state of the art and cost effective solutions to end users and partners.

    Formed in 1987 by Sandy Allan and Alex Sim the company’s first offices were in Madrid, Spain. Over the following three years further offices were opened in Italy, Switzerland and the UK. During the formative years of existence AMS helped launch the successful sales campaigns of Stratagene and Invitrogen providing them with an important foothold from which to develop their global brand expansion.
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