oxylogix

The Science Behind the System

This is not generic hydrogen peroxide vapour.
Only our proprietary formulation ensures proper disinfection.

Why chemistry matters more than vapour

Vaporising hydrogen peroxide alone does not guarantee reliable bio-decontamination.

Hydrogen peroxide is inherently unstable. Once dispersed, it rapidly decomposes into water and oxygen, limiting the duration and intensity of antimicrobial activity. This results in variable performance, particularly in real-world environments with complex airflow, surface geometry, and organic load.

Our proprietary formulation contains precisely controlled concentrations of silver, which fundamentally change the chemistry of the vapour phase.

Silver acts as a catalyst, accelerating the formation of highly reactive hydroxyl radicals during diffusion. These radicals are responsible for rapid and effective disruption of microbial cell membranes, proteins, and genetic material.

The result is significantly enhanced microbial kill, achieved through chemistry, not simply contact.

These limitations become most visible in mould remediation, where spores are specifically adapted to survive brief oxidative exposure and re-establish once conditions stabilise. In these environments, vapour delivery alone is insufficient. The chemistry must remain active long enough to prevent recovery and regrowth. This principle applies universally, but mould-affected spaces expose failure first.

Catalysed radical generation

The inclusion of silver enables controlled and sustained hydroxyl radical formation during diffusion. This produces a higher and more consistent antimicrobial effect than hydrogen peroxide alone, without increasing corrosivity or material stress.

This consistency is critical in environments where organisms are resilient and exposure conditions are imperfect.

Extended antimicrobial action

While hydrogen peroxide alone ceases activity once decomposition occurs, silver-catalysed formulations maintain antimicrobial effectiveness for longer during treatment and leave trace residues that inhibit microbial re-establishment on treated surface.

This extended activity is essential in environments where re-colonisation can occur once treatment ends.

Validated performance

The solutions are tested and validated as formulations, not concepts. Log reduction claims, exposure parameters, and treatment protocols are all based on this specific chemistry.

Substituting the formulation invalidates those outcomes, particularly in applications where performance margins are narrow and failure is not immediately visible.

High-risk clinical environments

» Patient rooms and isolation areas.

» Post-discharge bio-decontamination between occupants.

» Reduces environmental bioburden and supports consistent infection control.

Patient rooms and isolation areas

Post-discharge bio-decontamination between occupants.

This reduces environmental bioburden and supports consistent infection control.

Outbreak containment

Rapid environmental bio-decontamination during norovirus, C. difficile, or MDRO events.

Enables fast containment without prolonged disruption to clinical operations.

Operating theatres

Scheduled and between-case decontamination in surgical environments.

Reaches complex equipment, fixtures, and airflow systems beyond manual cleaning.

Aged care facilities

Routine environmental biosecurity in high-risk residential settings.

Supports infection prevention without introducing moisture or corrosive chemicals.

Verification and outcomes

Biosecurity is only meaningful when it can be verified. Oxylogix protocols generate documented evidence of effectiveness using established microbiological validation methods and environmental monitoring.

Biological indicators

Standardised spore strips containing known quantities of test organisms are used to confirm that protocol parameters achieved the intended level of microbial reduction.
Independent third-party laboratory analysis provides objective verification, removing subjectivity from effectiveness claims.

An established biosecurity methodology

Chemical indicators track vapour concentration and distribution throughout the treatment space, confirming uniform exposure in real time.
When combined with biological validation, this creates comprehensive documentation suitable for regulatory audit, quality assurance, and compliance reporting.