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Pegasus™ Grade LV6 Virus Removal Filter Cartridges

Large Virus Removal Filter with High Flow Performance

The risk of large virus contamination is a common feature of biologic products. Potential sources of large virus contamination (retroviruses, for example) of biotechnology
products include viruses associated with the cell lines (endogenous viruses), or viruses introduced into the cell line or product during the production process (adventitious viruses).

Large viruses like HIV could potentially be present in donations for plasma derivatives. Pegasus Grade LV6 AB-style Filter Cartridges with Ultipleat® construction
provide an efficient and economical method for removing large viruses like Retroviruses with > 6 log titer reduction or larger virus antibody complexes from biological solutions. The unique Pegasus LV6 membrane in combination with the patented Ultipleat filter construction provides robust high flow rates and total throughput performance which minimizes process costs. The high filter area per filter cartridge reduces the required amount of filter elements per installation and minimizes the hold up volume of the virus filter system. The proven hydrophilic PVDF microporous membrane enables high transmission of proteins also for larger proteins. The filter is delivered pre-sterilized and prewetted which reduces handling time.

Features and Benefits

 

  • Robust virus retention
  • > 6 log TR for large viruses
  • High flow rate and total throughput performance
  • High filter area per filter cartridge
  • Less filter elements per installation and minimized virus system hold up volume
  • Low binding for high protein yields
  • High protein transmission
  • Pre-sterilized and pre-wetted easy to use
  • SIP and CIP able
  • 100% integrity tested (correlated to virus retention)
  • Manufactured for use in conformance with cGMP
  • Pharmaceutical P-optimized with Certificate of Test provided
  • Validation Guide available

High Quality Standards

 

  • Non-Fiber-Releasing per 21 CFR
  • Meets USP Biological Reactivity, in vivo, for Class VI-121 °C plastics
  • Meets Cleanliness per USP Particulates in Injectables
  • Non-Pyrogenic per USP Bacterial Endotoxins (< 0.25 EU/mL)
  • Meets Total Organic Carbon and Conductivity per USP Purified Water, pH per USP packaged waters