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- Sartopore Evo® | 0.2µm | Cartridge (Production | Small to Large Scale)
Sartopore Evo® | 0.2 µm | Cartridge | 20"
Sartopore Evo® cartridges are designed for small- and large-scale GMP production, providing efficient filtration and meeting the rigorous demands of biopharmaceutical manufacturing. Their innovative PES membranes ensure high flow rates and minimal adsorption, meeting stringent industry standards.
- Item No.:
- 5992507G2
- Piece
- 1
Sartopore Evo® cartridges are designed for small- and large-scale GMP production, providing efficient filtration and meeting the rigorous demands of biopharmaceutical manufacturing. Their innovative PES membranes ensure high flow rates and minimal adsorption, meeting stringent industry standards.
Overview
Specifications
Choose your Sartopore Evo®
Sartopore Evo® marks the next generation of high-performance, sterilizing-grade filters for pharmaceutical and biopharmaceutical fluids. An innovative modification of polyethersulfone (PES) membranes minimizes the adsorption of proteins and excipients, such as polysorbates, to ensure stable drug formulations and reduce the number of vials that must be discarded during form and fill operations.
Unlike the polyvinylidene fluoride (PVDF) membrane filters, Sartopore Evo® does not intentionally use PFAS compounds in its construction material.
In addition, Sartopore Evo® filters achieve much higher flow rates and throughputs than PVDF membrane filters, allowing the use of a smaller filter element, further reducing adsorption and disposable waste.
Main Applications and Process Steps
Sterilizing-grade filtration of bulk drug substance and final filtration of drug product in applications like:
- Monoclonal antibodies (mAbs)
- Adeno-associated virus (AAV)-based therapies
- Lipid nanoparticles (LNPs)
Features and Benefits
- Minimized adsorption of proteins and excipients, like polysorbate 20 and 80, to increase yield and ensure stable drug formulation, supporting compliance with specifications
- High filter capacity and flow rates for efficient process operations
- No intentional use of PFAS compounds, protecting the long-term supply security of critical components
Membrane
Sartopore Evo® uses a double double layer membrane made of polyethersulfone.
The combination of the built-in 0.8 μm pre-filter in front of a 0.2 μm final filter enables outstanding overall flow and flow rate performance in the target applications.
Unique Surface Modification
The Sartopore Evo® filter's unique surface modification is fundamental to its robust performance. This feature minimizes the adsorption of proteins and excipients, such as polysorbates, which are commonly used in drug formulations. The adsorption of these components can lead to significant challenges, including reduced drug efficacy and stability. By effectively reducing adsorption, the Sartopore Evo® filter ensures that the integrity and potency of the drug product are maintained throughout the filtration process and significantly reduces lost batches due to deviations from formulation specifications. This increases the process yield and reduces costs.
Sterilization
Sartopore Evo® cartridges have been developed for sterilization using either autoclaving (134°C | 30 min. | 3 cycles) or in-line-steaming (134°C | 20 min. | 3 cycles) and are delivered non-sterile.
Flexibility
Sartopore Evo® filters are available in a wide range of filtration areas from 4.5 cm² up to 2.4 m² and with a variety of commonly used connections to ensure easy integration into your process regardless of batch size.
Scalability
Consistent and predictable scale-up and scale-down procedures are ensured with Sartopore Evo® filter elements, as they are all crafted using the same membrane type, support fleeces, and construction materials, providing reliability across applications.
Environmental Impact
Unlike PVDF filters, the Sartopore Evo® is made without the intentional introduction of PFAS compounds. As regulatory pressures mount against PFAS due to their potential health and environmental risks, the Sartopore Evo® filter provides a future-proof solution that aligns with global sustainability goals.
This ensures that manufacturers can confidently meet regulatory requirements and maintain a reliable supply chain while maintaining the highest standards of product safety and efficacy.
Accessories Information
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AdapterBottom: 2-Flange Bayonet w. 226 double o-ring | Top: S-Adapter
Applications
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Application
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mAB Production
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Vaccine Production
- Viral Vector Vaccine
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mAB Production
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ModalityForm & Fill
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ScaleProduction | Large Scale
Compliance Information
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Bacterial Endotoxins< 0.25 EU/mL as determined by the LAL test
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ExtractablesThe total amount of extractables is well below the limits established by the current USP unter "Sterile Water for Injection".
Dimensions
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Filter Size20"(1.6 m² / 17.2 ft²)
General Specifications
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Capsule/Cartridge FormatCartridges
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Maximum Diffusion44 mL/min
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Minimum Required Bubble Point3.3 bar | 47.9 psi
Materials of Construction
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Housing MaterialPolypropylene (PP)
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Material o-ring | sealSilicone (SI)
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Membrane MaterialPolyethersulfone (PES)
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Support FleecePolyester (PET)
Operating Conditions
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Maximum Differential Pressure20 °C: 5 bar, 80 °C: 2 bar
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Maximum Operating Pressure5 bar (72.5 psi)
Physicochemical Information
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Pore Size Final-filter0.2 µm
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Pore Size Pre-filter0.8 µm
Product Information
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BrandSartopore Evo®
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Pack Size1
Sterility/Purity
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Delivery ConditionNon sterile - Autoclavable | Steamable
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Sterilization MethodAutoclavable & In-Line Steam Sterilizable
Usage Protocols
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Sterilization ProceduresIn-Line Steam Sterilization: at 134 °C, 20 min., 2.3 bar, min. 3 CyclesAutoclaving: at 134°C, 30 min, 2 bar, min. 3 cycles