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The Pathologist / Issues / 2026 / September / Kidney Testing Gets Under the Skin
Biochemistry and molecular biology Screening and monitoring Technology and innovation

Kidney Testing Gets Under the Skin

A microneedle platform captured a kidney injury biomarker from interstitial fluid

09/22/2026 News 3 min read
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Objective:

To evaluate a microneedle patch for measuring the kidney injury biomarker neutrophil gelatinase-associated lipocalin in dermal interstitial fluid.

Approach:
  • Patch Development: A patch with 121 antibody-coated microneedles was developed to capture neutrophil gelatinase-associated lipocalin from interstitial fluid.
  • Testing in Mice: The patch was first evaluated in mice with lipopolysaccharide-induced acute kidney injury, showing increased biomarker levels within four hours.
  • Human Testing: In healthy volunteers, paired interstitial fluid and plasma measurements were taken, showing strong correlation despite lower concentrations in interstitial fluid.
  • Storage Stability: Patches were coated with zeolitic imidazolate framework-8 to improve storage stability, retaining 94% of fluorescence signal after temperature cycling.
Key Findings:
  • Neutrophil gelatinase-associated lipocalin levels increased in interstitial fluid before changes in serum creatinine.
  • The assay had a detection limit of 16 pg/mL in mouse samples and 9 pg/mL in human samples.
  • The patch left small skin openings that healed within 30 minutes.
  • Protected patches maintained assay sensitivity after temperature cycling and transport.
Interpretation:

Interstitial fluid could serve as an alternative matrix for minimally invasive kidney biomarker testing.

Limitations:
  • The study did not test the patch in patients with kidney disease.
  • The current system requires post-removal processing, not being a fully self-contained test.
  • Sample-specific reference ranges are needed due to lower concentrations measured by the patch compared to serum.
Conclusion:

Further studies are required to establish clinically actionable thresholds and assess diagnostic performance in patients.

Sources:
  • Advanced Materials

This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.

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