# Development of thin-film micro-outlets for spatially constraining local PO2 perturbations to capillaries in vivo

**Authors:** Meghan E. Kiley, Richard J. Sové, Reilly H. Smith, Brenda N. Wells, Gaylene M. Russell McEvoy, Graham M. Fraser

PMC · DOI: 10.3389/fphys.2025.1575776 · 2025-07-09

## TL;DR

Researchers developed thin-film micro-outlet devices to precisely control oxygen levels in small muscle regions and observed effects on capillary blood flow.

## Contribution

The novel composite thin-film micro-outlet devices enable localized manipulation of oxygen concentration to study microvascular responses in vivo.

## Key findings

- Oxygen oscillations via 400 μm micro-outlets significantly altered capillary RBC oxygen saturation and supply rate.
- 200 μm micro-outlets also caused significant changes in RBC oxygen saturation and supply rate at low oxygen levels.
- The devices spatially confined oxygen perturbations to affect only capillaries directly overlying the outlets.

## Abstract

To develop and validate thin-film micro-outlet devices to study microvascular blood flow responses to localized changes in skeletal muscle oxygen concentration ([O2]).

30 male Sprague-Dawley rats (159–194 g) were anesthetized and instrumented to maintain cardiovascular state. The extensor digitorum longus (EDL) muscle was dissected, isolated, and reflected over a gas exchange chamber (GEC) mounted in the stage of an inverted microscope. The GEC and EDL were coupled via a composite, gas permeable membrane, and a gas impermeable film fabricated with laser machined micro-outlets of specific diameters (200, 400, 600, and 1,000 μm). [O2] in the EDL was dynamically manipulated with step-wise oscillations between 7% (1 min) → 12% (1 min) → 2% (1 min) → 7% (1 min), and step challenges from 7% (1 min) → 2% or 12% (2 min), while recording intravital video for capillary RBC oxygen saturation (SO2) and hemodynamic measurements. Oxygen diffusion between tissue and micro-outlet devices was modelled using a finite element mass transport model to further validate experimental results.

[O2] oscillations imposed on capillaries directly overlying 400 μm micro-outlets caused significant changes in RBC SO2 at 12% and 2% [O2], compared to 7% [O2] (p < 0.0001). [O2] oscillations caused significant changes in capillary RBC supply rate (SR) at 2% [O2] versus 7%, and were significantly different at 2% compared to 12% [O2] (p < 0.0014). Similarly, [O2] challenges imposed on capillaries overlying 200 μm micro-outlets also caused significant changes in RBC SO2 at 2% [O2], compared to 7% [O2] (p < 0.0001), and caused significant changes in SR at 2% [O2] compared to 7% (p < 0.0001).

Our composite thin-film devices were fabricated and validated to spatially confine oxygen perturbations to capillaries using micro-outlets of varying diameters. These results demonstrate that our devices can manipulate capillary SO2 and alter capillary RBC SR in vessels directly overlying the micro-outlet without affecting capillary SO2 at a distance from the outlets. Our novel composite thin-film micro-outlet devices demonstrate that capillary blood flow responses can be provoked by manipulating [O2] in tissue regions as small as ∼200 μm in diameter.

## Full-text entities

- **Chemicals:** SO2 (MESH:D013458), PO2 (MESH:C093415), O2 (MESH:D010100)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12283586/full.md

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Source: https://tomesphere.com/paper/PMC12283586