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Tecan Resolvex M10-96 Manual Positive-Pressure Solid Phase Extraction System

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Brand Tecan
Origin USA
Model M10-96
Channel Configuration 96-channel parallel processing
SPE Format Column-based (1 mL, 3 mL, 6 mL cartridges) and 96-well plate-compatible
Flow Rate Control 0.1–30 mL/min (adjustable via dual-range pressure regulation)
Sample Capacity Up to 96 samples per run
Sample Load Volume 0.05–2 mL per channel
Solvent Compatibility Unlimited solvent types (including acetonitrile, methanol, ethyl acetate, dichloromethane, hexane, and aqueous buffers)
Wetted Materials PTFE, polypropylene (PP)
Regulatory Compliance Designed for GLP/GMP-aligned workflows

Overview

The Tecan Resolvex M10-96 is a manually operated, positive-pressure solid phase extraction (SPE) system engineered for high-throughput, reproducible sample preparation in regulated and research-intensive laboratories. Unlike vacuum-driven SPE manifolds—whose flow rates vary significantly across channels due to differential resistance and column clogging—the Resolvex M10-96 applies uniform, controllable nitrogen or compressed air pressure across all 96 positions simultaneously. This ensures consistent elution kinetics, minimizes breakthrough risk, and improves inter- and intra-run precision—particularly critical for viscous biological matrices (e.g., plasma, serum, tissue homogenates) and complex environmental extracts. Its dual-range pressure regulation architecture enables fine-grained control over flow dynamics: low-pressure mode (0.1–5 mL/min) supports gentle conditioning and washing of sensitive sorbents (e.g., mixed-mode ion exchange or hydrophilic-lipophilic balance phases), while high-pressure mode (5–30 mL/min) accelerates solvent displacement during elution without compromising recovery or column integrity.

Key Features

  • 96-position parallel processing with independent flow path isolation per channel, eliminating cross-contamination and enabling heterogeneous sample sets (e.g., varying matrix types or analyte concentrations) within a single run
  • Dual-range positive-pressure control: precise manual adjustment via calibrated pressure regulators for both low-flow (5 mL/min) SPE steps
  • Universal compatibility with standard SPE consumables—including 1 mL, 3 mL, and 6 mL cartridges as well as 96-well format SPE plates—reducing method transfer overhead and consumable inventory complexity
  • Chemically inert wetted materials (PTFE seals, PP manifolds, stainless-steel pressure lines) ensure long-term stability with aggressive organic solvents and acidic/basic aqueous mobile phases
  • Compact footprint (28 × 35 × 22 cm) and tool-free cartridge/plate mounting design support benchtop integration in space-constrained QC labs and core facilities
  • No electrical power or software required—ideal for use in fume hoods, cleanrooms, or field-deployable mobile labs where electromagnetic interference or validation burden must be minimized

Sample Compatibility & Compliance

The Resolvex M10-96 accommodates diverse sample types ranging from 50 µL to 2 mL per channel, including plasma, urine, milk, honey, soil extracts, wastewater filtrates, and plant tissue digests. Its pressure-stable architecture maintains consistent residence time on sorbent beds—even with high-viscosity or particulate-laden samples—thereby enhancing analyte retention and reducing variability in recovery. The system complies with fundamental requirements of ISO/IEC 17025:2017 (clause 7.2.2 on method validation), ASTM D5673 (for environmental water analysis), and USP chromatographic system suitability guidance when used as part of a validated sample preparation workflow. While the instrument itself does not generate electronic records, its mechanical operation supports full traceability when paired with paper-based or LIMS-integrated SOPs—including documented pressure settings, solvent lot numbers, column batch IDs, and operator signatures.

Software & Data Management

As a fully manual, non-electronic platform, the Resolvex M10-96 operates without embedded firmware, touchscreen interfaces, or proprietary software. This eliminates cybersecurity risks, software validation requirements (e.g., FDA 21 CFR Part 11), and version-control dependencies common in automated systems. All operational parameters—including applied pressure, dwell times, solvent sequences, and column lot tracking—are recorded externally using laboratory notebooks, Excel-based run logs, or LIMS modules. For laboratories requiring digital audit trails, the device integrates seamlessly with electronic lab notebook (ELN) platforms via standardized metadata tagging (e.g., “SPE_M10-96_RunID_20240521_A01”) and barcode-scanned consumable identifiers.

Applications

  • Clinical and preclinical bioanalysis: robust cleanup of plasma, CSF, and dried blood spot extracts prior to LC-MS/MS quantification of small-molecule drugs, metabolites, and biomarkers
  • Multi-omics sample prep: orthogonal fractionation of polar and non-polar metabolites from cell lysates or microbial cultures using sequential SPE chemistries (e.g., WCX → C18)
  • Food safety testing: selective isolation of pesticide residues, mycotoxins, and veterinary drug contaminants from composite food matrices (e.g., baby formula, infant cereals, meat homogenates)
  • Environmental monitoring: enrichment and cleanup of trace-level PAHs, PCBs, and pharmaceuticals from surface water, sediment pore water, and atmospheric particulate filters
  • Forensic toxicology: high-reproducibility extraction of opioids, stimulants, and novel psychoactive substances from hair, oral fluid, and postmortem tissues

FAQ

Is the Resolvex M10-96 compatible with 96-well SPE plates?

Yes—it accepts standard ANSI/SLAS-format 96-well SPE plates with 1 mL or 2 mL well capacity, in addition to individual cartridges.
What pressure source is required?

A regulated nitrogen or compressed air supply (0–100 psi output range) with oil-free filtration is recommended; a standard lab-grade gas regulator with dual-stage pressure control suffices.
Can I use aggressive solvents such as DCM or THF?

Yes—wetted components are constructed from PTFE and polypropylene, which exhibit excellent chemical resistance to halogenated solvents, strong acids (≤6 M HCl), and bases (≤2 M NaOH).
Does Tecan provide validation documentation or IQ/OQ protocols?

Tecan supplies a comprehensive User Manual and Material Declaration (RoHS/REACH); site-specific IQ/OQ templates are available upon request for GxP-regulated environments.
How often should the pressure regulator and seals be maintained?

Under typical usage (≤5 runs/week), PTFE seals require replacement every 12 months; regulators should be calibrated annually per ISO 6145-4 guidelines.

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