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Home/Applications/In Vitro Diagnostics/Clinical chemistry analyzer
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Clinical chemistry analyzers: switching sample, reagent and wash-fluid paths

Application guide

Switching sample, reagent and wash-fluid paths is a specific liquid-handling operation in clinical chemistry analyzers. This page explains product responsibilities, sequence, actual conditions and recovery requirements. Establish the architecture before comparing configurations.

Application guide

Clinical chemistry analyzer

Clinical chemistry analyzer
Diaphragm pumps in clinical chemistry analyzers
Probe/cuvette wash supply and waste removal
Bubble and pressure detection in clinical chemistry analyzers
Tubing and fittings in clinical chemistry analyzers
Multiport rotary valves in clinical chemistry analyzers
Sample, reagent and wash-path switching
Piston pumps in clinical chemistry analyzers
Metered reagent dispensingSample aspiration and transfer
Sampling and wash probes in clinical chemistry analyzers
Syringe pumps in clinical chemistry analyzers

On this page

Where sample, reagent and wash-fluid switching occurs in the instrumentProduct responsibilities in this operationOrganize the sequence by actual architectureDefine operating conditions for this taskCompare product configurations by the roles on this pageValidate operation results at the receiverLocate abnormalities and restore the next operationReferencesRelated guides

01Where sample, reagent and wash-fluid switching occurs in the instrument

Use a port-state table to manage reagent, sample, cleaning and waste destinations. Remove shared-channel residue after switching before the next task; check unintended connections using dead volume, flushing volume and valve-position feedback.

A port-state table should include pump actions, receiving containers and permissible pressure. Shared residue remains after the valve reaches position; the next liquid and assay residue requirements determine whether and how much to flush.

02Product responsibilities in this operation

Valves control the current source or destination; the associated drive performs metering or transfer. Port connections, actual positioning and shared-segment renewal must match the operation.

For this operation, confirm: Sample, reagent, wash and waste port states; receiving cuvette; permitted switching pressure; shared liquid inventory; flushing destination and first-dose arrival.

03Organize the sequence by actual architecture

  1. Create a port-state table for sample, reagent, wash fluid and waste, confirming current source, destination and isolated branches in each entry.
  2. Switch under instrument-permitted pressure and pump states, verify valve position and actual connection, then perform the corresponding aspiration/dispensing action.
  3. Direct old shared-segment liquid to its specified destination and confirm target-liquid arrival before connecting the reaction cuvette; check unintended connections, leaks and backflow.

04Define operating conditions for this task

Conditions, results and abnormality records for this operation
To defineDetails
Actual operating conditionsSample, reagent, wash and waste port states; receiving cuvette; permitted switching pressure; shared liquid inventory; flushing destination and first-dose arrival
Acceptance targetTest each source-to-cuvette route for unintended connections, leakage and backflow. After a source change, measure the liquid needed to clear the shared segment and confirm the first useful dose reaches the intended cuvette.
Fault localizationA valve may reach position while old sample, reagent or wash fluid remains downstream. Wrong port mapping, backflow or incomplete replacement can therefore change the next cuvette even when the command completes.

Further technical reading

  • Rotary Valve Selection Guide: From Fluid Paths to System Validation
  • Choosing Rotary Valve Wetted Materials: Head, Rotor and Seals

05Compare product configurations by the roles on this page

Configuration options for the product roles on this page
ProductConfiguration optionConditions to verify
MRV3 multiport rotary valveMultiple-source selectionCompare 10-, 16- and 24-port options and port diagrams; verify high-pressure suitability separately
  • MRV3 multiport rotary valve

    MRV3 multiport rotary valve

    View Details

06Validate operation results at the receiver

Test each source-to-cuvette route for unintended connections, leakage and backflow. After a source change, measure the liquid needed to clear the shared segment and confirm the first useful dose reaches the intended cuvette.

Use the next sample or reagent and the assay-relevant blank or high/low sequence to assess residue. Record flushing consumption separately from the volume accepted by the reaction cuvette.

07Locate abnormalities and restore the next operation

A valve may reach position while old sample, reagent or wash fluid remains downstream. Wrong port mapping, backflow or incomplete replacement can therefore change the next cuvette even when the command completes.

Suspend the affected route and identify its source, valve state and cuvette. Establish whether any liquid entered that cuvette, route recovery liquid to the specified waste path, and verify replacement and first-dose delivery before resuming.

Valve position establishes a connection state, not sample suitability or an accepted reaction dose. The assay determines how to handle a cuvette with uncertain composition or partial delivery.

References

View references (1)
  1. [1]FOREACH MRV3 multiport rotary valve: configurations and specifications

Related guides

  • Back to the clinical chemistry analyzer fluidics overview
  • Multiport rotary valves in clinical chemistry analyzers

Related Products

MRV3 Rotary valves

MRV3 Rotary valves

Related Technical Articles

Rotary Valve Selection Guide: From Fluid Paths to System Validation

Map the connections required at each step before comparing specifications. Use the actual liquids, tubing and switching sequence to validate suitability for your instrument.

2026-09-30View Details

Choosing Rotary Valve Wetted Materials: Head, Rotor and Seals

Identify every component in contact with liquid before comparing PEEK, PCTFE and other candidates. Evaluate chemical compatibility, dynamic sealing and analytical results together.

2026-09-30View Details

Discuss Your IVD Fluidic Requirements

Share the instrument type, sample and reagent properties, working volumes, cycle timing, fluid path and acceptance criteria so we can discuss suitable components and prototype evaluation.

Discuss your application