ArticleNature communications2025
A nanoMIP sensor for real-time in vivo monitoring of levodopa pharmacokinetics in precision Parkinson's therapy.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Nanomaterial -enabled flexible sensors for continuous biomedical monitoring and closed-loop intervention.Discover nano · 2026Review
- Multifunctional Hybrid Nanomedicines for Neurodegenerative Diseases: A Paradigm Shift from Rational Design to Clinical Translation.International journal of nanomedicine · 2026Review
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Authors and funding
11 authors.
Funding
Abstract
Real-time in vivo monitoring of levodopa pharmacokinetics is essential to address its narrow therapeutic window in Parkinson's disease (PD) therapy. However, current methods require excessive sample volumes, suffer low sampling frequencies, and fail to capture complete pharmacokinetic profiles. Here, we present an in vivo monitoring system for real-time tracking of levodopa levels in interstitial fluid (ISF) using a spindle-shaped carbon nanotube (CNT) fiber electrochemical sensor functionalized with a nanoscale molecularly imprinted polymer (nanoMIP) on single electroactive CNTs. The core-shell (CNT-nanoMIP) nanostructures provide sensitive, selective detection of levodopa, along with resistance to both biofouling and chemical fouling in continuous ISF detection. The system was validated for monitoring complete pharmacokinetic profiles and assessing temporal correlations between ISF/plasma levodopa pharmacokinetics in both PD rat models and healthy rats. We also demonstrated optimized and adjustable pharmacokinetic profiles through in vivo experiments with rationally designed levodopa dosing regimens, highlighting the system's potential for personalized PD pharmacotherapy.
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