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Thermo Scientific Vanquish Core Ultra-High-Performance Liquid Chromatograph

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Brand Thermo Scientific
Origin Germany
Manufacturer Type Original Equipment Manufacturer (OEM)
Import Status Imported
Model Vanquish Core
Instrument Type Ultra-High-Performance Liquid Chromatograph (UHPLC)
Launch Date March 2020

Overview

The Thermo Scientific Vanquish Core UHPLC system is an engineered platform for robust, reproducible, and regulatory-compliant liquid chromatographic analysis in pharmaceutical, biopharmaceutical, clinical research, and quality control laboratories. Built on the proven Vanquish architecture and manufactured in Germany, it employs high-pressure binary pumping (up to 1000 bar), low-dispersion flow paths, and thermally stabilized optics to deliver precise gradient delivery, exceptional retention time stability, and high-resolution separations. Its design adheres to core chromatographic principles—utilizing isocratic and gradient elution with real-time pressure and temperature compensation—to ensure method transfer fidelity and analytical continuity across instruments and labs. The system supports both reversed-phase and hydrophilic interaction liquid chromatography (HILIC), and is fully compatible with sub-2-µm particle-packed columns for enhanced peak capacity and sensitivity.

Key Features

  • System Health Check: Automated pre-run diagnostic routine scheduled daily, weekly, or monthly—verifying pump integrity, detector lamp status, autosampler valve timing, and solvent degassing performance to proactively identify deviations before sequence execution.
  • Diagnose Guide: Context-aware, step-by-step interactive troubleshooting interface accessible via touchscreen; guides users through hardware-level verification of UV lamp intensity, grating alignment, stepper motor response, seal tightness, and detector baseline noise—reducing dependency on field service engineers.
  • Intelligent Solvent Monitoring: Real-time volumetric tracking of mobile phase reservoirs using integrated level sensors and flow-based consumption modeling—prevents dry-pump conditions and eliminates unplanned run interruptions due to solvent depletion.
  • Adjustable Gradient Delay Volume (GDV): Hardware-controlled, continuously tunable GDV (range: 0–500 µL) enables true physical emulation of legacy HPLC and third-party UHPLC systems—ensuring identical gradient arrival times at the column head, critical for validated method transfer under ICH Q5A and USP .
  • 6-Channel Binary Pump: Dual-piston, high-pressure binary gradient system with six solvent selection valves—enabling flexible mobile phase composition without manual solvent switching or external switching valves.
  • Dual-Channel UV/Vis Detector: Simultaneous dual-wavelength absorbance detection with thermally stabilized optical path and low-noise photodiode array electronics—supporting ratio monitoring, peak purity assessment, and baseline correction in compliance with FDA 21 CFR Part 11 data integrity requirements.
  • Smart Touchscreen Interface: Corrosion-resistant, glove-compatible 10.4-inch capacitive display with embedded video-guided maintenance modules—including seal replacement, flow cell cleaning, and needle seat reconditioning—all localized in English with timestamped version control.
  • Advanced Sample Injection Logic: Programmable injection volume, needle wash cycles, and pressurized pre-injection compression—minimizes carryover, improves peak symmetry (asymmetry factor <1.2), reduces solvent mismatch effects, and extends column lifetime by mitigating pressure shock during needle insertion.

Sample Compatibility & Compliance

The Vanquish Core accommodates standard 0.5–2 mL vials, 96-well and 384-well microplates, and custom sample containers via optional adapters. It supports aqueous, organic, and mixed mobile phases—including TFA, HFBA, and ammonium acetate buffers—within pH 1.0–12.0 and operating temperature range 5–80 °C. System validation documentation complies with ASTM E2656 (Standard Practice for Validation of Liquid Chromatography Systems), ISO/IEC 17025:2017 (General Requirements for Competence of Testing and Calibration Laboratories), and EU GMP Annex 11. Audit trail, electronic signatures, and secure user access levels are natively supported in Thermo Scientific Chromeleon CDS v7.3+ for GLP/GMP environments.

Software & Data Management

Controlled exclusively via Thermo Scientific Chromeleon Chromatography Data System (CDS) v7.3 or later, the Vanquish Core integrates with LIMS and ELN platforms through standardized ODBC and RESTful API interfaces. All method parameters, instrument logs, and raw data files (.RAW) are stored with immutable timestamps and checksum-verified integrity. Electronic records include full audit trail metadata (user ID, action timestamp, parameter before/after values), meeting FDA 21 CFR Part 11 and EU Annex 11 requirements for electronic records and signatures. Batch processing, report templating, and automated QC flagging (e.g., pressure drift >5% over 10 injections) are configurable without scripting.

Applications

The Vanquish Core delivers consistent performance in small-molecule quantitation (e.g., residual solvents per ICH Q3C), peptide mapping for monoclonal antibody characterization, impurity profiling in drug substance batches (ICH Q3B), dissolution testing per USP , and stability-indicating assays under forced degradation conditions. Its gradient fidelity and retention time reproducibility (<0.02 min RSD over 100 injections) make it suitable for compendial methods requiring strict system suitability criteria (e.g., USP tailing factor ≤2.0, resolution ≥2.0). It is routinely deployed in QC release testing workflows aligned with ISO 17025 accreditation scopes.

FAQ

Does the Vanquish Core support method transfer from Agilent or Waters UHPLC systems?
Yes—via hardware-adjustable gradient delay volume and pressure-compensated flow control, enabling physical equivalence—not software interpolation—of gradient profiles across platforms.
Is Chromeleon CDS validation documentation available?
Yes—Thermo provides IQ/OQ/PQ protocols, installation qualification checklists, and 21 CFR Part 11 configuration guides as part of the system delivery package.
Can the system operate unattended for extended sequences?
Yes—integrated solvent monitoring, predictive health checks, and automatic needle wash routines enable 72+ hour unattended operation with full audit trail logging.
What column oven temperature accuracy does the Vanquish Core provide?
±0.2 °C over 5–80 °C range, verified per ASTM E2656 Annex A3 thermal uniformity testing protocol.
Is remote monitoring supported?
Yes—Chromeleon Remote Access enables secure web-based instrument status viewing, log review, and limited method editing via TLS 1.2 encrypted connection.

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