Protein Concentration Tangential Flow Filtration System

Protein Concentration Tangential Flow Filtration System

Jiuling designs and supplies Tangential Flow Filtration (TFF) systems for downstream bioprocess applications including protein concentration, buffer exchange, and purification preparation.

  • Product Introduction
 

Company Overview

 

Jiuling designs and supplies Tangential Flow Filtration (TFF) systems for downstream bioprocess applications including protein concentration, buffer exchange, and purification preparation.
Each system is configured based on process conditions such as flow rate, membrane selection, and automation level, rather than fixed equipment models. This approach helps maintain consistency during scale-up and routine production.

 

 

System Principle

 

The system operates on tangential flow filtration, where the feed stream flows parallel to the membrane surface under controlled crossflow conditions.
This reduces direct particle accumulation and helps maintain stable filtration performance over long operating cycles.
Compared with dead-end filtration, this method is more suitable for protein solutions that require structural stability and high recovery rates.

 

 

Technical Specifications

 

Parameter

Specification

Filtration Mode

Tangential Flow (Crossflow)

Application

Protein concentration / diafiltration / purification prep

Membrane Types

Hollow fiber / flat sheet / spiral wound

MWCO Range

1 kDa – 1000 kDa (customizable)

Filtration Area

0.1 m² – 20 m²+

Operating Pressure

Up to 6 bar

Temperature Range

4–40°C

Flow Mode

Recirculation / single-pass optional

Pump Type

Peristaltic / diaphragm / centrifugal

Control System

PLC-based (Siemens or equivalent)

Monitoring

Pressure / flow / TMP / temperature

Materials

316L stainless steel + biocompatible tubing

Cleaning

CIP / SIP optional

 

 

Engineering Advantages

Reduced Scale-Up Risk
Lab, pilot, and production systems follow the same filtration principle. Scale-up is achieved through membrane area expansion rather than process redesign, reducing validation effort and transfer uncertainty.
Stable Process Performance
Crossflow operation helps maintain consistent flux behavior during long runs, reducing sudden performance drop caused by membrane fouling.
Protein Stability Protection
Operating conditions are designed to reduce mechanical stress, supporting stable recovery of sensitive proteins such as monoclonal antibodies and recombinant proteins.
Process Integration Compatibility
The system can be integrated into existing upstream and downstream lines without changing overall process architecture.

 

 

Core Functions

 

Protein Concentration
Concentrates target biomolecules by removing water and low molecular weight impurities while maintaining protein stability under controlled shear conditions.
Diafiltration (Buffer Exchange)
Supports continuous buffer replacement without precipitation or centrifugation, improving control over formulation conditions.
Pre-Chromatography Preparation
Reduces feed volume and improves homogeneity before chromatography, supporting more stable column loading performance.

 

 

Process Position in Bioprocess Workflow

 

The system is typically used in the downstream process chain:

  • Cell culture harvest
  • Clarification
  • TFF concentration and buffer exchange
  • Intermediate purification preparation
  • Chromatography feed conditioning

By standardizing feed quality before chromatography, it helps improve downstream process consistency and reduce variability between batches.

 

 

System Selection Logic

 

01/

Membrane Selection
Hollow fiber: Suitable for shear-sensitive proteins and high recovery requirements
Flat sheet cassette: Fexible use in development and pilot scale
Spiral wound: Preferred for high-volume and cost-sensitive processes

02/

Automation Level
Manual: Process development and small-scale testing
Semi-automatic: Controlled operation with monitoring
PLC automated: GMP production with batch consistency requirements

03/

Process Mode
Recirculation: Batch concentration and controlled processing
Single-pass: Continuous processing with higher throughput demand

04/

GMP Configuration
Recommended when process requires:
CIP/SIP compatibility
Batch data recording
Validation support for production use

 

 

Typical Operation Workflow

 

System Preparation & Flush: Automated flushing and sanitization of the membrane loop.
Feed Transfer: Controlled transfer of the clarified harvest from the bioreactor or buffer tank.
Concentration Phase: Crossflow circulation with real-time, automated TMP adjustments to safely drive volume reduction.
Diafiltration Phase (Optional): Automated buffer addition matches permeate removal rate for precise salt or buffer exchange.
Product Recovery: Low-holdup volume recovery of the final concentrated intermediate into formulation or storage vessels.

 

 

Packaging and Delivery

Every Jiuling system is engineered and packed to withstand rigorous international transit conditions:
Skid-Mounted Frame: Compact, rigid stainless-steel frame, securely anchored for long-distance maritime or air freight.
Component Protection: High-grade shock isolation for sensitive instruments, PLC enclosures, and pumps.
Environmental Sealing: Moisture-resistant, anti-corrosion barrier packaging for all tubing, valves, and membrane connection ports.
Pre-Shipment Verification: Comprehensive Factory Acceptance Testing (FAT) conducted prior to dispatch. Systems can be delivered as a fully assembled single skid or modular assemblies for restricted-space on-site installation.

 

 

FAQ

 

Q: Is it suitable for monoclonal antibody production?

A: Yes. It is widely used for antibody concentration and buffer exchange under controlled shear conditions.

Q: How is scale-up managed?

A: Scale-up is achieved by increasing membrane area while keeping the same process principle, reducing process redevelopment risk.

Q: What membrane types are available?

A: Hollow fiber, flat sheet cassette, and spiral wound depending on process needs.

Q: Does it support GMP production?

A: Yes. GMP-oriented configuration with PLC control, CIP/SIP, and documentation support is available.

Q: What is the operating pressure range?

A: Up to 6 bar depending on system configuration.

Q: Can the system be automated?

A: Yes. PLC-based automation with recipe control is available.

Q: How is the system delivered?

A: Skid-mounted or modular configuration depending on installation requirements.

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