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Virosart® CPV Minisart®

The PES based virus filter for robust and efficient removal of small non-enveloped and large enveloped viruses in biopharmaceutical applications. Virosart® CPV is the optimal virus filter for monoclonal antibodies or small recombinant proteins.

Integrity Tested
Item No.: 
545VM----------B
Availability: 

*Custom/bulk order quotes are provided within 72 hours of request.

Tutorial

Virosart® HC & Virosart® CPV Minisart® Lab Scale Product Tutorial

Learn how to install and perform virus filtration. You will also receive recommendations on handling to improve the final filtration.

Watch Training Video

Application:

  • Virus clearance: Virosart® CPV retains ≥ 4 LRV of small non-enveloped viruses (e.g. PPV, MVM) and ≥ 6 LRV of large enveloped viruses (e.g. MuLV).
  • Target molecule: The main applications for Virosart® CPV for virus filtration are monoclonal antibodies (mAb), antibody fragments (Fab) or small recombinant proteins (< 150 kD).
  • Positioning: Virosart® CPV is used towards the end of the purification process of biopharmaceutical products for the virus filtration. At this stage, the purity of the biopharmaceutical product is at its highest and so fouling of the filter by contaminants (DNA, CHOP, aggregates & lipoproteins) will be low.

Product Benefits:

  • Robust virus clearance: Virosart® CPV retains ≥ 4 LRV of small non-enveloped viruses (e.g. PPV, MVM) and ≥ 6 LRV of large enveloped viruses (e.g. MuLV). This filter offers highest virus safety over the entire flow decay profile independently of operating pressure.
  • Smart process transfer: Flexibility is given by using either cartridges in existing stainless steel housings or disposable capsules.
  • Ease of use: Virosart® CPV are tested for integrity using a water-based diffusion test, e.g. based on the Sartocheck® technology of Sartorius Stedim Biotech

Regulatory Compliance

  • Validated for ≥ 4 LRV removal of small non-enveloped viruses using bacteriophage PP7
  • Designed, developed and manufactured in accordance with an ISO 9001 certified Quality Management System
  • Meet or exceed the requirements for WFI quality standards set by the current USP
  • Non pyrogenic according to USP Bacterial Endotoxins
  • USP Plastic Class Test VI

Applications

  • Application
    • mAB Production
    • Recombinant Protein Production

Connections (Physical)

  • Connector Inlet
    Luer Lock
  • Connector Outlet
    Luer Lock

Dimensions

  • Filtration Area
    5 cm²

Features

  • Integrity Tested
    No

General Specifications

  • Capsule/Cartridge Format
    Down scale unit
  • Filter Format
    Down Scale Units

Materials of Construction

  • Filter Material
    Polyethersulfone (PES)

Physicochemical Information

  • Pore Size
    20 nm (nominal)

Product Information

  • Brand
    Virosart® CPV
  • Pack Size
    5

Sterility/Purity

  • Delivery Condition
    Non sterile - Autoclavable