Resilient nanostructured bioanalytic microneedle longitudinally monitors preclinical renal and hepatic drug clearance and dysfunction

Wearable microneedle biosensors promise real-time molecular monitoring for precision medicine but are limited by low sensitivity and tissue abrasion. Overcoming these challenges, we recast electrode functionality not merely as a sensing substrate but as a mechanism for resilient, high signal-to-noise ratio (SNR) measurements in tissue. Our microneedle-based resilient nanostructured bioelectrode (RNB) is fabricated using a bilayer process that strengthens the electrode with a micrometer-thick gold adhesion layer and reduces fabrication-induced stress through controlled dealloying. The resulting RNBs are corrosion resistant, stable over a wide potential window, and have an artifact-free, nanocavity-textured interface. They integrate receptor-based electrochemical biosensors with enhanced SNR through increased active area, diffusion, and antifouling while remaining abrasion immune in megapascal-stiff tissues. The RNB extended in vivo biosensor lifetime for pharmacokinetics monitoring to 6 days in a freely moving rat. Paired with a blood-interstitial fluid equilibrium-based bioanalytical framework, the RNB accurately derived blood-equivalent pharmacokinetic parameters, enabling not only precision dosing of narrow therapeutic index drugs but also the direct assessment of hepatic and renal clearance. In hepatic studies, the RNB revealed delayed clearance of a chemotherapeutic (irinotecan) in liver-damaged models. In renal studies, RNB recordings correlated with blood antibiotic pharmacokinetics across chronic kidney disease severities. The RNB detected renal impairment earlier than conventional biomarker thresholds through drug clearance quantification and captured recovery under therapeutic intervention. These results establish the RNB as a viable microneedle platform for high-fidelity in vivo deployment of electrochemical biosensors, enabling minimally invasive, longitudinal monitoring of low-concentration analytes and real-time assessment of organ function.

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Publication Details

Journal
Science Translational Medicine
Published
2026-04-01
DOI
https://doi.org/10.1126/scitranslmed.adr5493
Citations
2
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
Field-Weighted Citation Impact
28.74

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article

Resilient nanostructured bioanalytic microneedle longitudinally monitors preclinical renal and hepatic drug clearance and dysfunction

Benjamin M. Wu, Jagotamoy Das, Shana O. Kelley, M. Bahman Bahramian et al.
2 citations
Science Translational Medicine
Advancements in Transdermal Drug Delivery
28.74
article

Resilient nanostructured bioanalytic microneedle longitudinally monitors preclinical renal and hepatic drug clearance and dysfunction

Benjamin M. Wu, Jagotamoy Das, Shana O. Kelley, M. Bahman Bahramian, Boyu Hu, Kuanming Yao, Sam Emaminejad, David Jelínek, Hilary A. Coller, Ira Kurtz, Xuanbing Cheng, Yitian Chi, Laurent Voisin, Aaron Ambrus, Kiarash A. Sabet, Zongqi Li, Carlos Milla, Hanie Yousefi, Kaiji Zhang, Tsung‐Yu Wu, Nanthia Suthana, Chong Liu, Jialun Zhu, Y Zhao, Yifu Li, Anthony Sung, Jiarui Cui, Yu Chen, Joshua Ng, Shuyu Lin, Isabel Romero, Ryan Chaiyakul, Jiawei Tan
article en
2 citations

Abstract

Wearable microneedle biosensors promise real-time molecular monitoring for precision medicine but are limited by low sensitivity and tissue abrasion. Overcoming these challenges, we recast electrode functionality not merely as a sensing substrate but as a mechanism for resilient, high signal-to-noise ratio (SNR) measurements in tissue. Our microneedle-based resilient nanostructured bioelectrode (RNB) is fabricated using a bilayer process that strengthens the electrode with a micrometer-thick gold adhesion layer and reduces fabrication-induced stress through controlled dealloying. The resulting RNBs are corrosion resistant, stable over a wide potential window, and have an artifact-free, nanocavity-textured interface. They integrate receptor-based electrochemical biosensors with enhanced SNR through increased active area, diffusion, and antifouling while remaining abrasion immune in megapascal-stiff tissues. The RNB extended in vivo biosensor lifetime for pharmacokinetics monitoring to 6 days in a freely moving rat. Paired with a blood-interstitial fluid equilibrium-based bioanalytical framework, the RNB accurately derived blood-equivalent pharmacokinetic parameters, enabling not only precision dosing of narrow therapeutic index drugs but also the direct assessment of hepatic and renal clearance. In hepatic studies, the RNB revealed delayed clearance of a chemotherapeutic (irinotecan) in liver-damaged models. In renal studies, RNB recordings correlated with blood antibiotic pharmacokinetics across chronic kidney disease severities. The RNB detected renal impairment earlier than conventional biomarker thresholds through drug clearance quantification and captured recovery under therapeutic intervention. These results establish the RNB as a viable microneedle platform for high-fidelity in vivo deployment of electrochemical biosensors, enabling minimally invasive, longitudinal monitoring of low-concentration analytes and real-time assessment of organ function.

Science Translational MedicineVol. 18(843)
Florida State University (US), Northwestern University (US), Boston Children's Hospital (US), California NanoSystems Institute (US), University of California, Los Angeles (US), Duke University (US), Somerville Hospital (US), McCormick (United States) (US), Chan Zuckerberg Initiative (United States) (US), Stanford Medicine (US), Samueli Institute (US), Center for Pain and the Brain (US), BioElectronics (United States) (US), Chan Zuckerberg Biohub Chicago, Massachusetts Institute of Technology (US)
Cystic Fibrosis Foundation, National Institutes of Health, University of California, Los Angeles, California NanoSystems Institute
Openalex Percentile: Top 0%
Advancements in Transdermal Drug Delivery
28.74
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