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Sartocon® Slice Disposable Hydrosart® Cassette

Hydrosart® membranes are extremely hydrophilic, making it non-protein binding and virtually non-fouling. Hydrosart® mikrofiltration cassettes are available in 0.2 µm and 0.45 µm.

Item no.:  3061860701W--SW

Availability:  On Request

Hydrosart® is a stabilized cellulose derivative membrane polymer that has been optimized for the biotechnological and pharmaceutical industries. The Hydrosart® membrane is a stable polymer that features a broad pH and temperature range. Hydrosart is also extremely hydrophilic, making it non-proteinbinding and virtually non-fouling. As a result, it has extremely high flux. Hydrosart®’s wide temperature range makes it possible to sterilize the membrane by either steam or autoclaving. Membrane regeneration, storage and depyrogenation can be accomplished by using NaOH even at elevated temperatures. Hydrosart® membranes are designed for use in the biotechnological and pharmaceutical industries.

They can be used to remove the following from liquids:

  • Mammalian cells: CHO BHK
  • Bacteria: E. coli Pasteurella C. diphtheria
  • Yeasts
  • Cell Iysates Product

Hydrosart® has minimal adsorption of proteins, viruses, etc. Membrane retention is unaffected by repeated re-use. Hydrosart® has been validated to withstand in-line steam sterilization without any loss of integrity or changes in membrane retention.

Datasheet

Hydrosart® Microfiltration Cassettes — Cell harvest and bacteria concentration
en 217.3 kB

User Manual

Manual_Sartocon_Cassettes_SPC6051-a.pdf
en 2.0 MB

Product properties

  • Cassette Format
    Slice Disposable
  • Flow Channel Geometry
    Microfilter Wide Spacer
  • Primary Product Type
    Filters
  • Filter Format
    Cassettes
  • Filter Type
    Crossflow Filters
  • Filtration Area
    0.1 m²
  • Pore Size
    0.2 µm
  • Membrane Filter Material
    Hydrosart®

Technical attributes

  • Bacterial Endotoxins
    < 0.18 EU/mL as determined by the LAL test
  • Filter Class
    Microfilter
  • Biosafety
    All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
  • Extractables
    The total amount of extractables is well below the limits established by the current USP unter "Sterile Water for Injection".
  • Integral Frame
    Polyvinylidene fluoride (PVDF)
  • Non-Fiber Releasing
    This filter product complies with the title 21 of the Code of Federal Regulations (CFR), section 210.3(b)(6) and 211.72.
  • Sealing Compound
    Silicone White (High chemical resistance)
  • Spacer
    Polypropylene (PP)
  • pH Stability
    pH 2 – 14
  • Maximum Inlet Pressure
    4 bar
  • Industry
    Pharma/Biotech