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AXF Series

Micropore Technologies

Micropore’s technology enables scalable formulation of mono-disperse microspheres, nanoparticles and emulsions from lab bench to GMP manufacture significantly accelerating the efficiency of nanomedicine development.
Manufacturer Micropore Technologies
Product Series AXF series
Application Emulsions, Liposome Processing & Mixing, Nanoparticle formulation
Sample type Nanomedicines, Microspheres, Polymer nanoparticles, Crystals, Liposomes, Nucleic acid lipid nanoparticles (LNPs)
Formulation Technology Advanced crossflow (AXF™) mixing
Particle size distribution Narrow (typical CV~10%)
Volumes formulated 0.2ml upto 1500L/hr

The Micropore AXF series uses advanced crossflow mixing technology to enable the continuous production of particles. This fully scalable, GMP-ready platform is the ideal method for developing and manufacturing microcapsules, emulsions, nanoparticles and crystals whilst retaining a tightly controlled particle size distribution.

Micropore’s technology employs laminar flow across a precision engineered stainless steel membrane.  The outer dispersed phase is continuously mixed with the aqueous inner compartment to form particles with very narrow particle size distributions. Both reliable and reproducible, the small footprint (<A4) and aseptic design allows it to be used where high levels of hygiene and sterilisation including GMP are important.

Gentle processing preserves the stability of material to enable the continuous manufacturing of high-quality formulations in quantity for a wide range of applications, from precise self-assembly, in the case of liposomes or Lipid nanoparticles (LNPs), to the control solvent exchange during crystallisation. Micropore manufacturing platform has produced uniform LNPs with an encapsulation efficiency >97% and has the capacity to manufacture flow rates of up to 1500L/hr – by far the fastest production rate available.

Choose from 3 configurations: 

AXF-mini (Discovery to Clinical)   AXF-1 (Manufacturing) AXF-n (Large Scale Manufacturing) 
Production capacity: 0.06-20L/hr

Disperse phase hold-up volume: 0.1mL

Continuous phase hold-up volume: 0.3mL

Production capacity: 6-200L/hr

Disperse phase holdup volume: 5mL

Continuous phase hold-up volume: 5mL

Production capacity: up to 1500L/hr

Disperse phase hold-up volume: 20mL

Continuous phase hold-up volume: 100mL

Resources

Continuous, scalable

  • Streams of mono-dispersed particles at controllable dimensions with a narrow particle size distribution (typical CV~10%)

Low maintenance, No cartridges

  • Low-cost operation,  with no moving parts, that are easy to clean
  • Small equipment footprint (able to fit into a small briefcase)
  • SS316 & PTFE parts for high material compatibility and simple sterilisation

High Volume, GMP ready

  • Throughput volumes from discovery phase through to clinical and manufacturing (0.06L/hr-1500L/hr)

Efficient Cross Flow Mixing

  • Preservation of biological activity of biomolecules after encapsulation
  • Up to 30% lower energy usage compared to other emulsion generation methods

Micropores membrane technology is ideal for creating complex formulations and to solve formulation challenges to deliver the highest performing, most efficient, cost-effective formulated delivery systems.

Micropore’s patented crossflow membrane technology is used in applications including pharmaceuticals/ medicines, food/ nutrition, cosmetics/ skincare, household products, agrochemicals/ farming, battery development and construction.

Some of the most recent applications include:

  • Fragrance encapsulation

Fragrance chemicals can be found in laundry detergents, soaps and personal care products, however fragrances exhibit high volatility and rapidly lose their aroma or, worse, transform into unpleasant odours, if subject to prolonged atmospheric exposure. Microencapsulation of the fragrance material applies a protective coating. Micropore Encapsulation technologies can provide the repeatability, reproducibility and fine control not previously offered by historic emulsification techniques.

  • API Crystallisation

Crystallisation defines an APIs physical properties and ability to deliver the desired therapeutic effect and to avoid undesirable effect  Micropore’s robust continuous membrane technology can eliminate many of the issues faced by both batch cooled and anti-solvent approaches to crystallisation and is scalable to tonnes per hour.

  • Core-shell coacervation in drug delivery

Complex coacervation involves the microencapsulation of products where the core is surrounded by a shell (2 – 300 μm) which protects it against degradation while enabling control over payload delivery under specific conditions. Eg. Selective encapsulation of therapeutic nucleotides, such as miRNA mimics, small interfering RNAs, and transcripts to accommodate a wide range of therapeutic strategies including inhibition of atherogenic miR-33a in atherosclerosis.

  • Hydrogels in drug delivery & biomedical engineering

Hydrogels consist of tunable 3D, hydrophilic, polymeric networks that protect labile drugs from degradation and assist their controlled release. Currently, hydrogels are used for manufacturing contact lenses, hygiene products, wound dressings, tissue engineering scaffolds and drug delivery systems. Micropores’ Membrane emulsification overcomes many existing production challenges by forming hydrogel droplets directly as a w/o emulsion. Precise size control can be achieved with perfectly spherical droplets in sizes less than 50μm.

  • Liposomes & Lipid nanoparticles (LNPs)

Liposomes and LNPs are amphiphilic structures used as drug delivery vehicles to encapsulate both hydrophilic and hydrophobic active pharmaceutical ingredients (APIs). LNPs have gained prominence recently due to their ability to deliver therapeutic payloads, including DNA and mRNA for vaccines, precisely through treating their surface with proteins allowing highly specific binding to a target cell type.

Evaluation of AXF Pathfinder and Horizon Mini™ for Poly(A) and mRNA Lipid Nanoparticle Production”

  • Sustained release PLGA microspheres

PLGA (Poly (lactic acid-co-glycolic acid)) is used for surgical implants and sutures because of its biodegradability, biocompatibility and sustained-release properties. However PLGA is not easy to formulate into sustained release drug products meaning inventor drug products and generic versions remain scarce with only 20 drugs approved in 30+ years. Micropore’s technology is an inherently gentle process that results in very high-quality microspheres when using a double emulsion process, because the primary emulsion is not broken during secondary emulsification. Micropore’s continuous manufacturing technology offers no risk in scaleup. No product degradation – Right size first time – Reduced compliance issues.

  • Silica particles

Mesoporous silica particles (MSP) have gained wide popularity over recent years because of their advantages of uniform and tunable pore size, easy independent functionalisation of the surface, internal and external pores and the gating mechanism of the pore opening make it a distinctive drug carrier. Their high loading capacity due to the large pore volume and surface engineering properties allows for better drug targeting. These versatile carriers can be used for loading a variety of cargos ranging from drugs to macromolecules such as proteins, DNA and RNA.

  • Phase Change Materials

Phase change materials (PCMs) allow the storage of large amounts of latent heat during phase transition. They have the potential to both increase the effciency of renewable energies such as solar power through storage of excess energy, and to reduce overall energy demand through passive thermal regulation. NASA has identified more than a hundred of these materials. In addition to passive energy storage, they have application in thermoregulated fabrics, high power electronics, telecommunication installations and microprocessors. PCMs are not suitable for use without prior encapsulation. Encapsulation in a shell material provides benefits including protection of the PCM from the external environment and increased specific surface area to improve heat transfer.

  • Battery Materials & Electrodes

AXF membrane emulsification technology enables precise, scalable control of uniform droplet formation for templating engineered battery particles. This allows tight tuning of particle size, morphology, and internal structure in materials such as lithium titanate, lithium iron phosphate, and composite nanomaterials. The result is highly uniform, spherical secondary particles with improved packing density, easier slurry processing, and reliable scale-up. By bridging nanoscale design with industrial manufacturing, AXF supports enhanced ion transport, higher volumetric energy density, and more consistent electrochemical performance in advanced lithium-ion batteries.

Microdroplet Templating of Uniform Nanostructured Battery Microparticles with Scalable Membrane Emulsification – Published in ACS Nano (2026)

What is advanced crossflow mixing?

Advanced crossflow (AXF™) mixing is a precise, low-shear membrane technology used to create emulsions, suspensions, and lipid nanoparticles (LNPs) with extremely tight size distributions. By passing fluids across a precision-engineered membrane, it offers continuous, scalable, and contamination-free mixing for pharmaceutical, cosmetic, and food applications

How does crossflow technology work?

Advanced Crossflow (AXF) mixing technology formulates nanoparticles through controlled fluid dynamics rather than traditional batch methods, enabling precise and reproducible nanoparticle production.

What applications is AXF series suitable for?

The AXF series is suitable for producing liposomes, lipid nanoparticles (LNPs), polymer nanoparticles, microspheres, and crystalline materials, primarily for genomic medicine and drug delivery applications.

What is the throughput capacity of the AXF series?

Full customisable the AXF series delivers sample volumes that start in the range of 0.2 mL to 250 mL depending on the model and can operate very high throughput up to 1500 L/hr.

The AXF series can be added to the automated Pathfinder and Horizon systems which achieve high reproducibility through controlled AXF mixing, delivering narrow particle size distributions with a coefficient of variation of approximately 10% and encapsulation efficiency typically exceeding 98%.

What types of nanoparticles can be produced with the AXF series?

The AXF series can produce liposomes, lipid nanoparticles (LNPs), polymer nanoparticles, microspheres, crystalline materials and more.

Why is the AXF series important for nanoparticle formulation development?

The AXF series provides GMP-ready nanoparticle production from day one, helping researchers and companies scale from R&D to clinical manufacturing seamlessly without switching to a different technology platform. It has the capacity to use a formulation created on virtually any other platform to distinguish optimal scale up conditions.

How is the AXF series different from microfluidic approaches?

Unlike traditional microfluidic approaches such as Impingement Jet Mixing, the AXF series uses lower shear and vanishingly low pressure, crucial for maintaining the stability of delicate formulations like mRNA-LNPs. It uses a single, reusable, consistent technology throughout development, keeping production costs low without expensive consumables. Constructed from durable 316L stainless steel, it allows thorough industrial cleaning and sterilisation, making it ideal for GMP environments.

Who uses the AXF series?

Biotech companies, pharmaceutical developers, and academic labs focused on nanomedicine research use the AXF series for drug delivery, vaccine development, gene therapy, and other nanomedicine applications.

Can I have a demonstration or free trial of the AXF series?

Yes, if a system is available. Contact us for a booking. We can arrange a personalised demo and test your samples within our lab facility in Sydney. Onsite free trials are also available. Contact us or complete a request a demo form to get started.

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