MIOPC™

One workflow for rare-cell enrichment and observation.

A planned microfluidic platform for CTC enrichment, enumeration and imaging in longitudinal cancer treatment-monitoring research.

Concept render of the planned MIOPC integrated instrument
Planned integrated MIOPC™ instrumentConcept—not production hardware
Product intent

Blood-based CTC enrichment, enumeration and imaging for treatment-monitoring research.

Why integrate?

Reduce handoffs across the research workflow.

Rare-cell work can involve multiple instruments and manual transfers. MIOPC™ is being developed to connect core steps within a compact workflow, with the aim of improving consistency and preserving cells for visual analysis.

01

Sample handling

Controlled microfluidic paths manage low-volume biological samples.

02

Cell enrichment

An immunomagnetic research workflow concentrates candidate target cells.

03

Optical observation

Planned imaging supports enumeration and cell-level review.

Core workflow

4-i Model

Immunomagnetic enrichment of circulating tumour cells in blood samples using droplet microfluidics.

i1

Interaction

Bring antibody-conjugated immunomagnetic beads into contact with candidate CTCs.

  • Cell size and density
  • Surface markers
  • Antibody targets
i2

Incubation

Provide controlled time and droplet conditions for bead–cell binding.

  • Interaction time
  • Cell viability
  • Functional integrity
i3

Isolation

Use a magnetic field to retain bead-bound target cells and reduce background.

  • Magnetic separation
  • Washing or filtration
  • Target-cell enrichment
i4

Identification

Image, count and review enriched cells using optical and fluorescence methods.

  • Microscopy
  • Fluorescence detection
  • Cell profiling
01

Interaction + incubation

Droplet microfluidics brings the blood sample, reagents and cells together.

02

Isolation

Antibody-conjugated magnetic beads support selective enrichment.

03

Identification

Optical detection and CTC imaging provide measurable cell-level observations.

Research outputs

Designed for longitudinal CTC monitoring studies.

  • Determine CTC counts at defined timepoints
  • Differentiate candidate CTCs from white blood cells
  • Correlate CTC trends with treatment response
  • Support patient-specific monitoring research

Planned architecture

Instrument and assay components designed together.

These visuals communicate the intended product direction. Final industrial design, specifications and clinical performance are still under development.

Concept rendering of the planned MIOPC instrument
Instrument concept

Controlled processing and imaging

A compact housing concept for fluid handling, magnetic enrichment and optical observation.

Concept image. Configuration and specifications may change.

Concept rendering of the planned MIOPC assay kit components
Assay concept

Workflow-specific consumables

Cartridge and reagent components envisioned for repeatable sample preparation and processing.

Concept image. Not a currently marketed clinical kit.

Early analytical results

Recovery measured in controlled spiking studies.

Known quantities of cultured breast cancer cells were introduced into controlled samples and processed using the early immunomagnetic workflow.

81.8%

MCF-7 recovery

818 ± 28 cells recovered from 1,000 spiked cells.

89.3%

MDA-MB-231 recovery

893 ± 32 cells recovered from 1,000 spiked cells.

Interpretation: these preliminary results describe recovery under a controlled spiking protocol. They do not establish clinical sensitivity, specificity, patient validation, treatment-response prediction or clinical utility.

Prototype evidence

Current laboratory development.

Laboratory photographs are shown separately from concept renders so the present development stage remains clear.

Laboratory fluidic tubing and prototype imaging setup
Prototype fluid handling and optical bench
Fabricated Acrofluidic prototype chips
Fabricated microfluidic prototypes
Experimental microscopy image from Acrofluidic research
Experimental cell-level observation

Development status

Validation in measurable stages.

The pathway progresses from analytical repeatability toward appropriately designed clinical research.

01

Repeatability

Expand analytical runs, controls and operating-condition characterisation.

02

Matrix evaluation

Assess recovery and background effects in increasingly representative samples.

03

Integrated prototype

Connect enrichment, fluid control and optical observation in one workflow.

04

Clinical research

Evaluate performance and utility with partners under approved study protocols.

Research-stage platform

Clear evidence boundaries.

MIOPC™ is under development for research use. It is not cleared for diagnosis, treatment selection or patient management.

Interested in evaluating the platform?

We welcome conversations with oncology researchers, hospitals, translational labs and technology partners.

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