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Home/Applications/Synthetic biology/Microbioreactors
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Microbioreactors: Design Feeding, Sampling and Volume Balance Together

Application guide

Feeding and sampling can substantially change microbioreactor volume. Fluidic design should support records of cumulative additions, sample representativeness and contamination boundaries, beyond a single small-volume dispense test. Parallel reactors also require assessment of shared resources and path isolation.

Application guides

Microbioreactor application guide

Microbioreactor fluidics overview
Syringe pumps in microbioreactors
Sampling
Valveless metering pumps in microbioreactors
Feeding
Diaphragm pumps in microbioreactors
Air-containing waste aspiration and post-maintenance restart
Fluidic valves in microbioreactors
Path isolation
Bubble and pressure detection in microbioreactors
Tubing and Fittings for Microbioreactors

ON THIS PAGE

Locate the task in the fluid path firstCommon product roles and application guidesOperating requirements differ by stepFeeding: distinguish pulse and continuous modesSampling: account for representativeness and discard volumePath isolation: prevent unintended connections to culture vesselsWaste removal: specify biomass and foam conditionsMonitoring: incorporate fluid-path information into process recordsExplore configurations through product application guidesValidate the complete cycle through application resultsCommon selection and recovery questionsReferences

01Locate the task in the fluid path first

Culture medium and additives→Independent feeding→Microbioreactors→Sampling and analysis→Drainage and maintenance
Illustrative task sequence. Confirm sampling, washing, waste and monitoring branches separately against the instrument drawings.

Arrows indicate task relationships, not that every component is connected in series in one tube. Check valve positions, pump wetted boundaries and operating states for each branch.

For each feed, record mode, actual medium and cumulative volume. For each sample, record collected material, discarded volume and process-volume disturbance. Validate valve isolation, cleaning or sterilization, and backflow after shutoff separately.

02Common product roles and application guides

Explore product applications by their role in the instrument
Product categoryRole in this instrument
Syringe pumpPulse feeding and discrete sampling
Valveless metering pumpsRepeated or continuous feeding in suitable configurations
Diaphragm pumpSuitable air-containing waste aspiration
Fluidic valvesRouting for feeding, sampling and maintenance; tubing shutoff in feed or sample branches
Bubble and pressure detectionBranch-status signals for process records
Tubing and fittingsConnect feed sources, cultures and sample destinations
  • Syringe pumps in microbioreactors
  • Valveless metering pumps in microbioreactors
  • Diaphragm pumps in microbioreactors
  • Fluidic valves in microbioreactors
  • Bubble and pressure detection in microbioreactors
  • Tubing and Fittings for Microbioreactors

03Operating requirements differ by step

Define fluid-path responsibilities before examining individual operations
StageTask categoryOperating conditions to define
Feeding: distinguish pulse and continuous modesFeed mode and cumulative material balanceDiscrete or continuous feeding mode, time profile, medium, load, cumulative volume and permissible interruption
Sampling: account for representativeness and discard volumeSample renewal and representativenessAnalyte, sampling interval, renewal of stagnant sections, discard-volume budget and permitted pretreatment
Path isolation: prevent unintended connections to culture vesselsValve-path requirementsAll ports, valve states, pressures in each state, shared volume and flushing volume
Waste removal: specify biomass and foam conditionsActual drainage and vessel conditionLiquid or gas-liquid inlet conditions, peak incoming flow, allowable accumulation, lift and waste container
Monitoring: incorporate fluid-path information into process recordsInputs for fault detectionSpecific sensor configuration, location, liquid/tubing, sampling rate, threshold and time window

04Feeding: distinguish pulse and continuous modes

Adding the same cumulative volume at different times may alter the process. Translate batch, periodic-pulse or continuous requirements into allowable variation and interruptions before comparing drives.

  • Feeding

05Sampling: account for representativeness and discard volume

Renewing stagnant sections consumes liquid; small systems especially need a volume budget. Use paired sample analysis and reactor-volume records together to assess sampling.

  • Sampling

06Path isolation: prevent unintended connections to culture vessels

The port-state table must cover feeding, sampling, cleaning and drainage. Check leakage and backflow even in closed states.

  • Path isolation

07Waste removal: specify biomass and foam conditions

Confirm suitable conditions separately for air-containing aspiration and liquid-only drainage. After maintenance, check sealing and isolation before resuming culture operations.

  • Air-containing waste aspiration and post-maintenance restart

08Monitoring: incorporate fluid-path information into process records

Pressure and bubble alarms help assess branch anomalies; culture condition requires the relevant process measurements. Preserve cumulative-volume records through actual recovery procedures.

  • Bubble and pressure detection in microbioreactors

09Explore configurations through product application guides

  • Syringe pumps in microbioreactors
  • Valveless metering pumps in microbioreactors
  • Diaphragm pumps in microbioreactors
  • Fluidic valves in microbioreactors
  • Bubble and pressure detection in microbioreactors
  • Tubing and Fittings for Microbioreactors

10Validate the complete cycle through application results

Check cumulative feeding, sampling representativeness, volume balance and recovery during long runs.

Plan operating-point validation and fault investigation for each step
Step to validateMeasurements or observationsPriority troubleshooting checks
Feeding: distinguish pulse and continuous modesMeasure pulse doses or flow over defined time windows separately, then reconcile cumulative material, bottle changes and restarts.An empty source, bubbles, refill interruptions or repeated control states may alter actual feed delivery.
Sampling: account for representativeness and discard volumeMeasure renewal time at the analytical or receiving interface and assess target representativeness using paired samplesOld-sample mixing, settling, adsorption or insufficient renewal time can make the sample unrepresentative of its source.
Path isolation: prevent unintended connections to culture vesselsCheck unintended connections, leakage, backflow and post-switching residue in each state; measure flushing volume and arrival delay through the complete pathMisalignment, shared-segment residue or abnormal switching pressure may affect the next task
Waste removal: specify biomass and foam conditionsTest emptying, liquid accumulation and interlocks after a full-vessel or blockage condition using the actual incoming liquid.Leaks, foam, blockages or a full container can reduce actual drainage capacity.
Monitoring: incorporate fluid-path information into process recordsMeasure fault detection, false alarms and end-to-end response separately; cover baseline changes with liquid, speed and operating conditionsNormal air segments, viscosity changes and sampling delays may be misclassified

Bubble and pressure signals describe fluid-path conditions; they do not directly measure pH, dissolved oxygen or growth. Validate the complete aseptic boundary separately.

11Common selection and recovery questions

Does equal cumulative feed volume establish an equivalent feeding process?

Also compare addition timing, pulsed or continuous mode, permitted fluctuation and no-flow intervals. Validate individual doses or time-window flow first, then cumulative volume and process results.

Does sampling consumption equal only the volume collected in the analytical vessel?

Record path-renewal discard and other drainage together. Confirm any permitted return path, then check actual process volume and sample representativeness.

References

View references (4)
  1. [1]FOREACH syringe pumps: configurations and specifications
  2. [2]FOREACH RPL / DRPL valveless metering pumps: configurations and specifications
  3. [3]FOREACH Tubing-Pinch Options, Discussed by Project: Configurations and Specifications
  4. [4]FOREACH bubble / pressure detection: configurations and specifications

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HLD rotary-valve syringe pump; representative configuration. Select capacity, materials and interfaces for the application.

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RPL Valveless Metering Pump; representative configuration. Select capacity, materials and interfaces for the application.

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ABD bubble-detection module; representative configuration. Select capacity, materials and interfaces for the application.

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PDM5 pressure-detection module; representative configuration. Select capacity, materials and interfaces for the application.

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Discuss your microbioreactor fluidics

Provide a fluidic diagram, actual liquids and pressures in each operating state. Specify stroke, discarded volume and refills; actual load and cumulative volume; closure and contamination-control boundaries; and process stages and restart. Compare configurations against this guide's validation objectives.

Contact an engineer