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Thermo Fisher Dionex AS-AP Multifunctional Autosampler

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Brand Thermo Fisher
Origin USA
Manufacturer Thermo Fisher Scientific
Product Type Imported Instrument
Model AS-AP
Instrument Category Multifunctional Autosampler
Sample Capacity Up to 1152 positions (microtiter plate) / 81 vials (10 mL)
Injection Cycle Time <30 s for 5 µL injection
Precision RSD <0.3%
Fluidic Path Full PEEK™ construction
Needle Design Moving-needle architecture
Temperature Control 4–60 °C sample tray cooling
Integrated Pre-injection Analysis Conductivity & pH measurement
Automation Capabilities Automated internal standard addition, on-line dilution, pre-column derivatization, matrix removal, analyte preconcentration, fraction collection, re-injection, and sample ejection

Overview

The Thermo Fisher Dionex AS-AP Multifunctional Autosampler is an engineered component of the Ion Chromatography (IC) ecosystem, designed specifically to extend analytical flexibility, reproducibility, and throughput in regulated and research-grade laboratories. Operating on a moving-needle aspiration principle, the AS-AP delivers precise liquid handling across heterogeneous container formats—including 10 mL screw-thread vials, 96-well and 384-well microtiter plates—without mechanical reconfiguration. Its fully PEEK™ fluidic path ensures chemical inertness and compatibility with aggressive eluents, high-pH mobile phases, and trace-metal-sensitive applications common in environmental, pharmaceutical, and semiconductor water analysis. The system integrates directly with Thermo Scientific ICS series chromatographs and supports both sequential and parallel operation modes—enabling dual-IC method execution from a single autosampler platform while maintaining physical isolation of reagent streams to prevent cross-contamination.

Key Features

  • Moving-needle architecture enables consistent aspiration accuracy across variable vial heights and plate well depths, eliminating reliance on fixed-depth plungers or complex Z-axis calibration routines.
  • Full PEEK™ wetted components—including syringe, needle, rotor seal, and flow path—provide resistance to hydrolysis, oxidation, and metal leaching, critical for low-level anion/cation quantitation (sub-pptr detection).
  • Programmable sample tray temperature control (4–60 °C) maintains thermal stability for thermolabile analytes such as nitrite, iodide, or organic acids during extended unattended runs.
  • On-the-fly pre-injection characterization: integrated conductivity and pH sensors perform real-time assessment of sample integrity prior to injection, flagging outliers and reducing column fouling risk.
  • Dual-mode operation allows simultaneous servicing of two independent IC systems—each with dedicated valve routing, timing logic, and method-specific wash protocols—under centralized software control.
  • Automated sample conditioning: supports programmable internal standard spiking, serial dilution (1:2 to 1:1000), column pre-derivatization (e.g., o-phthalaldehyde for amines), solid-phase extraction (SPE)-based matrix removal, and analyte preconcentration via evaporation or trap-elute.

Sample Compatibility & Compliance

The AS-AP accommodates standard ANSI/SLAS-compliant microplates (96-, 384-, and 1536-well), 10–20 mL screw-cap vials, and custom tube racks. It complies with ISO/IEC 17025 requirements for automated sampling traceability and supports audit-ready electronic records per FDA 21 CFR Part 11 when deployed with Thermo Scientific Chromeleon™ CDS v7.3 or later. Method validation documentation—including precision (RSD <0.3% at n ≥ 6), carryover ( 0.999 over 4 orders of magnitude)—is available upon request for GLP/GMP environments. The system meets ASTM D4327 (anions in drinking water) and USP (conductivity of purified water) workflow prerequisites through its integrated pre-injection metrology.

Software & Data Management

Controlled exclusively via Chromeleon Chromatography Data System (CDS), the AS-AP leverages embedded method templates for common workflows: EPA Method 300.0/300.1 (drinking water anions), ISO 14911 (cation analysis), and pharmacopeial impurity profiling. All sequence parameters—including injection volume, rinse cycles, dwell times, temperature setpoints, and sensor-triggered conditional logic—are stored as encrypted, version-controlled objects. Audit trails record user actions, method changes, hardware events (e.g., needle clog detection), and sensor readings with timestamp, operator ID, and instrument signature. Data export conforms to ASTM E1384 and ISO/IEC 11179 metadata standards for LIMS integration.

Applications

  • High-throughput environmental monitoring: simultaneous analysis of NO₃⁻, SO₄²⁻, F⁻, Cl⁻, PO₄³⁻ in wastewater effluents with automated SPE cleanup and 100× preconcentration.
  • Pharmaceutical excipient testing: quantitative determination of residual acetate, chloride, and sulfate in APIs using suppressed conductivity detection and on-line pH correction.
  • Electronics-grade ultrapure water (UPW) qualification: sub-ppt Cl⁻ and Na⁺ detection with zero-sample-contact PEEK™ flow path and inert gas purged sample compartment.
  • Food safety screening: rapid quantification of preservatives (benzoate, sorbate) and biogenic amines (histamine, cadaverine) via post-column derivatization enabled by synchronized reagent delivery.
  • Academic research: method development for novel ionizable metabolites requiring iterative dilution, derivatization, and fraction re-analysis—all executed within a single sequence.

FAQ

Does the AS-AP support non-Thermo IC systems?
Yes—via analog/digital I/O and RS-232/RS-485 interfaces—but full feature parity (e.g., pre-injection pH/conductivity feedback, dual-system synchronization) requires native Chromeleon integration.
What maintenance intervals are recommended for the PEEK™ syringe and needle?
Under typical use (≤ 1000 injections/week), replace the syringe every 12 months and the needle every 6 months; lifetime extends significantly with low-salt, filtered samples.
Can the AS-AP perform gradient elution-compatible sample preparation?
No—the AS-AP handles only isocratic sample conditioning; gradient programming remains under the IC pump controller’s domain.
Is remote diagnostic capability available?
Yes—Chromeleon Remote Access enables secure, TLS-encrypted monitoring of status, error logs, and real-time sensor outputs from off-site locations.
How is carryover minimized during high-concentration sample analysis?
Three-stage needle wash (solvent A → solvent B → air purge) with pressure-assisted aspiration and dynamic dwell time scaling based on previous injection concentration.

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