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Ultrafiltration Membrane Filter For Separation Of Pharmaceutical Industry 5TPH Water Treatment System

  • Ultrafiltration Membrane Filter For Separation Of Pharmaceutical Industry 5TPH Water Treatment System
Place of Origin Shenzhen,Guangdong
Marca HJW
Certificação ISO 14001,ISO 9001,CE,EPA
Minimum Order Quantity 1set
Preço US$14700~US$15000
Packaging Details export standard wooden case
Delivery Time 1-7working days(depand on raw materials stocking)
Payment Terms L/C,D/P,T/T,Western Union
Supply Ability >300sets/month

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Detalhes do produto
Capacity 5m³/H（Customizable) Membrane Material RC, PES
Operating Pressure 0.5–3 bar Core process UF,RO,UV
Operation model PLC control Verified GMP/FDA/EMA
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Descrição de produto

I.Overview
Ultrafiltration (UF) equipment plays a key role in the pharmaceutical industry for separation, purification, concentration and pyrogen removal to meet the high purity requirements of drug manufacturing.
The core values are: high purity assurance (removal of pyrogens, viruses, impurities, compliant with pharmacopoeia standards), 
process flexibility (applicable to a wide range of products such as antibodies, vaccines, gene therapy, etc.), and design for compliance (meets the stringent validation requirements of GMP/FDA/EMA).


II.Typical Process Flow 


Monoclonal Antibody (mAb) Purification: 
Cell Culture Solution → Centrifugation/Deep Filtration → Ultra Filtration (30 kDa) → Protein A Chromatography → Viral Filtration → Ultra Filtration Dialysis (Liquid Exchange) → Preparation


Water for Injection (WFI) for pyrogen removal: 
purified water → multi-effect distillation / RO → ultrafiltration (10 kDa) → UV disinfection → storage and distribution


Concentration of viruses for vaccine production: 
Virus culture solution → microfiltration (0.22 μm) → ultrafiltration (300 kDa) → sucrose gradient centrifugation → inactivation/freeze-drying


III.Core Attribute Parameters

Performance Requirements for Ultrafiltration Membranes (Pharmaceutical Grade)
Parameter Pharmaceutical Grade Standard Description
Membrane Material Regenerated Cellulose (RC), PES RC: Low protein adsorption; PES: Resistant to acid-base cleaning.
Molecular Weight Cut-Off (MWCO) 1–300 kDa Antibody purification: 100 kDa; Pyrogen removal: 10 kDa.
Flux (LMH) 20–100 (Adjusted by Viscosity) High-viscosity feed (e.g., DNA) requires low flux.
Operating Pressure 0.5–3 bar Tangential Flow Filtration (TFF) mode reduces concentration polarization.
Integrity Test Bubble Point Test ≥3 bar Ensure membrane integrity; meet GMP validation requirements.
 Key Quality Control Indicators
Application Output Standard Regulatory Basis
Pyrogen Removal for Injections <0.001 EU/mL Chinese Pharmacopoeia 2020 Edition
Blood Products Viral Reduction ≥4 log (99.99%) FDA/EMA Viral Safety Guidelines
Biologics HCP ≤5 ppm ICH Q6B Quality Standar


IV.Core Application Areas 
Biologics Purification 
Blood Products Processing 
Injectable Pyrogen Removal 
Enzyme Concentration 
Chinese Medicine Modernization


V.Here is a guideline for you to get a proper quotation
Tell us the raw water/source of water(tap water, well water, or sea water, etc)
Provide water analysis report(TDS , conductivity, or resistivity, etc)
Required production capacity( 5m³/H, 50m³/H,or 500m³/H, etc)
What's the pure water used for( industrial,Food and Beverage,or agriculture, etc )



Etiquetas:

Sistemas industriais de ultrafiltração

Equipamento do Ultrafiltration

Sistema de