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Thermo Fisher Scientific Vanquish™ Duo Ultra-High-Performance Liquid Chromatography System

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Brand Thermo Fisher Scientific
Origin USA
Manufacturer Type Original Equipment Manufacturer (OEM)
Origin Category Imported
Model Vanquish™ Duo UHPLC Systems
Instrument Type Ultra-High-Performance Liquid Chromatograph
Price Range USD 65,000 – 130,000 (estimated FOB US)

Overview

The Thermo Fisher Scientific Vanquish™ Duo UHPLC System is an engineered dual-gradient ultra-high-performance liquid chromatography platform designed for method development acceleration, high-throughput routine analysis, and advanced hyphenated workflows—including serial LC, parallel LC, and LC-MS coupling. Built upon the proven Vanquish architecture, the Duo configuration integrates two fully independent, high-pressure gradient pump channels (up to 1500 bar), dual autosamplers, and shared or dedicated detection modules within a single compact chassis. Its core operational principle leverages precise binary or quaternary solvent delivery, low-dispersion flow paths, and sub-2 µm particle column compatibility to deliver exceptional resolution, retention time stability (<0.02 min RSD), and peak capacity across diverse analyte classes. The system is optimized for applications demanding rigorous reproducibility under regulated environments—particularly in pharmaceutical QC/QA, biopharmaceutical characterization, environmental monitoring, and food safety laboratories.

Key Features

  • Dual independent UHPLC channels housed in one integrated instrument footprint—reducing bench space by up to 40% versus two standalone systems.
  • Simultaneous operation of two distinct gradient methods: supports serial LC (e.g., online column regeneration during analysis), parallel LC (dual-column screening), and back-flush or heart-cutting 2D-LC configurations.
  • Each channel features a high-precision dual-piston pump with active solvent compressibility compensation, delivering flow accuracy ≤0.1% RSD and pressure pulsation <0.1% RMS at 1 mL/min.
  • Thermo Scientific™ Vanquish™ Flex Autosampler with 2 × 110-position vial capacity, cooled sample compartment (4–40 °C), and low carryover (<0.005%) via needle wash and seal-wash protocols.
  • Integrated thermostatted column compartment supporting dual columns (up to 150 mm length) with temperature control from 5–100 °C (±0.1 °C stability).
  • Native compatibility with electrochemical, UV-Vis diode array (DAD), fluorescence, charged aerosol (CAD), and mass spectrometric detectors—including seamless synchronization with Thermo Scientific™ Orbitrap™ and TSQ™ mass spectrometers.

Sample Compatibility & Compliance

The Vanquish Duo accommodates a broad range of sample matrices—including biological fluids (plasma, serum, tissue homogenates), purified proteins, small-molecule APIs, polymers, pesticides, and complex environmental extracts—without requiring hardware modification. Its fluidic design minimizes dwell volume (<100 µL per channel) and ensures robust performance with high-salt, viscous, or particulate-laden samples when paired with appropriate inline filtration. The system meets key regulatory requirements for GxP environments: it operates under validated Chromeleon CDS software compliant with 21 CFR Part 11 (electronic signatures, audit trail, user access controls), supports ALCOA+ data integrity principles, and is documented for IQ/OQ/PQ qualification. It aligns with ASTM D7928-21 (for polymer molecular weight distribution), USP (chromatography), and ISO/IEC 17025:2017 (testing laboratory competence) frameworks.

Software & Data Management

Control and data acquisition are unified through Thermo Scientific™ Chromeleon™ Chromatography Data System (CDS) 7.3 or later. The software provides dedicated method wizards for dual-channel setup—including synchronized injection timing, staggered gradient initiation, and real-time cross-channel status monitoring. All sequence parameters, instrument logs, raw data (.RAW), and processed results are stored in a secure, relational SQL database with configurable backup policies. Audit trails record every user action—including method edits, reprocessing events, and report generation—with immutable timestamps and operator IDs. Chromeleon supports automated report templates (PDF, Excel), electronic signature workflows, and direct export to LIMS or ELN platforms via ODBC or RESTful API. For LC-MS integration, the system enables real-time MS trigger synchronization and unified metadata tagging across both LC channels.

Applications

  • Pharmaceutical Development: Accelerated forced degradation studies using parallel acidic/neutral/basic mobile phases; simultaneous assay and impurity profiling under ICH Q2(R2) guidelines.
  • Biopharma Characterization: Dual-channel SEC-MALS and IEX analysis of monoclonal antibody aggregates and charge variants; online buffer exchange coupled with intact mass analysis.
  • Environmental Testing: High-throughput screening of PFAS compounds using serial LC-CAD with online column reconditioning—eliminating manual column switching downtime.
  • Clinical Research: Simultaneous quantification of vitamin D metabolites (D2/D3) and cortisol in dried blood spots via tandem LC-MS/MS with internal standard co-injection on separate channels.
  • Food & Beverage QA: Parallel analysis of mycotoxins and pesticide residues in grain extracts using orthogonal column chemistries (C18 vs HILIC) with shared CAD detection.

FAQ

Can the Vanquish Duo operate two completely different chromatographic methods simultaneously?
Yes—each channel maintains full autonomy in gradient profile, flow rate, column temperature, injection volume, and detector settings. Methods can be scheduled independently or coordinated via time-based triggers.
Is method transfer from single-channel Vanquish systems supported?
All Vanquish method files (.MTH) are natively compatible; dual-channel sequences require minor extension via Chromeleon’s Multi-Method Editor but retain identical retention time predictability and calibration curves.
Does the system support GMP-compliant audit trail and electronic signature functionality?
Yes—Chromeleon CDS is pre-validated for 21 CFR Part 11 compliance, including role-based permissions, biometric or PKI-based e-signatures, and tamper-evident audit logs with ≥10-year retention capability.
What detector interfaces are available for LC-MS coupling?
Standard ESI and APCI sources are supported via Thermo Scientific™ Ion Max™ NG interface; optional nano-ESI, HESI-II, and heated transfer line kits enable robust coupling to Orbitrap, Q Exactive, and TSQ series mass spectrometers.
How is column regeneration handled in serial LC mode?
While one channel performs analytical separation, the second channel executes a predefined regeneration protocol—including high-strength solvent flush, equilibration, and pressure stabilization—without interrupting ongoing data acquisition or requiring manual intervention.

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