AO2 SKIN — Clinical Research
Study overview

How oxygen nanobubbles help support healthier-looking skin

This study looked at whether delivering oxygen to the skin using oxygen nanobubble technology from AO2 SKIN can improve skin function without damaging or disrupting the skin barrier.

5
Study participants
3
Timepoints measured
60min
Study duration
Skin barrier intact

What is HIF-1α and why does it matter?

Your skin naturally has different oxygen levels at different depths. One important marker, called Hypoxia Inducible Factor-1 alpha (HIF-1α), helps scientists understand how much oxygen is available in the skin. When oxygen levels increase, this marker goes down.

In this study, participants applied oxygen nanobubbles of AO2 CLEAR to their skin. Small skin samples were taken before use, and again after 30 and 60 minutes. The results showed a clear decrease in HIF-1α, which means oxygen availability in the skin had improved dramatically.

Study timepoints

Baseline (T0)
30 min (T30)
60 min (T60)

Your skin barrier stays protected

Just as important, the skin itself remained intact. There were no detectable changes to skin structure or barrier integrity. Instead, the skin showed signs of a healthy, adaptive response, which is associated with stronger, more resilient skin over time.

Key takeaways

What this means for your skin

Supports better oxygen availability at the pore and follicle level

Helps create a healthier environment for skin function

Maintains skin barrier integrity

Encourages a more balanced, resilient complexion

This research supports how oxygen nanobubble technology from AO2 SKIN works to improve overall skin health in a gentle, non-disruptive way.

Research visuals

Seeing the science

Immunofluorescence microscopy images from the study, showing changes across the three measurement points.

HIF-1α immunofluorescence at T0, T30, and T60 showing reduction in expression
HIF-1α expression (T0 → T30 → T60) Reduction in HIF-1α levels — indicating increased oxygen availability in the skin following AO2 CLEAR application.
Filaggrin red staining at T0, T30, and T60 showing intact skin barrier
Filaggrin – red staining (T0 → T30 → T60) Confirms the skin barrier protein remained intact — no structural disruption from oxygen nanobubble treatment.
Peer-reviewed study

O₂ nanobubbles improve transcutaneous oxygenation without alteration to skin integrity

Immunofluorescence HIF-1α Filaggrin Transcutaneous oxygenation Skin barrier integrity Nanobubble technology

Abstract

This study aimed to evaluate whether topical delivery of oxygen nanobubbles (O₂ NB) from AO2 SKIN enhances oxygen availability in human skin tissue without compromising epidermal integrity.

Human skin is characterized by physiological oxygen gradients, with Hypoxia Inducible Factor-1 alpha (HIF-1α) serving as a central regulator of cellular response to oxygen availability. A reduction in HIF-1α expression is indicative of increased tissue oxygenation.

In this study, human skin biopsies were obtained from five volunteers following topical application of oxygen nanobubbles (AO2 CLEAR). Samples were collected at baseline, 30 minutes, and 60 minutes post-application. Immunofluorescence analysis was performed to quantify HIF-1α expression.

Results demonstrated a statistically significant reduction in HIF-1α levels following topical O₂ NB delivery, supporting improved transcutaneous oxygen availability.

In addition to oxygenation effects, analysis of five supplementary biomarkers indicated that O₂ NB exposure did not produce detectable structural alterations in epidermal integrity. Instead, findings suggest activation of a beneficial adaptive response consistent with physiological skin stress modulation.

These results support a dual mechanism of action: enhanced tissue oxygenation alongside adaptive cellular responses, contributing to improved skin resilience. This provides a scientific basis for the use of oxygen nanobubble technology in topical skincare applications.

Study design

5
Human volunteers
3
Biopsy timepoints
5
Supplementary biomarkers

Collection timepoints

Baseline (T0)
30 min post-application (T30)
60 min post-application (T60)

Analysis method

Immunofluorescence analysis was conducted by an independent academic institution in the United States. Findings are scheduled for presentation at a dermatology-focused scientific conference and submission for publication.

Key findings

Dual mechanism of action

Enhanced transcutaneous oxygenation
Statistically significant reduction in HIF-1α levels post-application

Preserved epidermal integrity
No detectable structural alterations in skin barrier markers

Adaptive cellular response
Activation of physiological skin stress modulation pathways

Improved skin resilience
Results support use in topical skincare applications

Immunofluorescence data

Research images

Immunofluorescence staining performed at T0, T30, and T60 following topical application of AO2 CLEAR oxygen nanobubbles.

HIF-1α immunofluorescence at T0, T30, T60 showing quantified reduction in expression
HIF-1α immunofluorescence (T0 / T30 / T60) Quantified reduction in HIF-1α expression demonstrating enhanced transcutaneous oxygenation over time.
Filaggrin red staining at T0, T30, T60 confirming maintained epidermal barrier integrity
Filaggrin – red staining (T0 / T30 / T60) Maintained epidermal structural integrity across all timepoints. Red channel confirms no disruption to the skin barrier.

Research integrity

Immunofluorescence analysis was conducted by an independent academic institution in the United States. Findings are scheduled for presentation at a dermatology-focused scientific conference and submission for publication.