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Updated: Jul 12, 2025

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Multiplex Therapeutic Drug Monitoring by Isotope-dilution HPLC-MS/MS of Antibiotics in Critical Illnesses
Published on: August 30, 2018
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Real-Time Monitoring of Antibiotics in the Critically Ill Using Biosensors
Ruvimbo Dephine Mishi1, Michael Andrew Stokes2, Craig Anthony Campbell3
1Department of Human Biology, Division of Cell Biology, University of Cape Town, Cape Town 7925, South Africa.
Antibiotics (Basel, Switzerland)
|October 27, 2023
Summary
Biosensors offer rapid, precise antibiotic measurement for critically ill patients. This technology enhances therapeutic drug monitoring (TDM), improving drug effectiveness and patient outcomes.
Area of Science:
- Pharmacology
- Biomedical Engineering
- Clinical Chemistry
Background:
- Therapeutic drug monitoring (TDM) is crucial for optimizing antibiotic dosing in critically ill patients to maximize efficacy and minimize toxicity.
- Current TDM methods face challenges including being time-consuming and slow, which limits their widespread application.
- Biosensors present a promising alternative for rapid and accurate drug concentration measurements.
Purpose of the Study:
- To review the current applications of biosensors for TDM of antibiotics in critically ill patients.
- To discuss both ex vivo point-of-care and in vivo continuous monitoring biosensor technologies.
- To address the clinical development, regulatory hurdles, and standardization needs for biosensor implementation.
Main Methods:
- Literature review of existing biosensor technologies for TDM.
- Analysis of ex vivo and in vivo biosensor designs for antibiotic monitoring.
- Discussion of clinical translation challenges and performance evaluation.
Main Results:
- Biosensors enable rapid, single-step quantification of drug concentrations.
- Both ex vivo and in vivo biosensor platforms are being developed for TDM.
- Standardization and regulatory approval are key factors for clinical adoption.
Conclusions:
- Biosensors hold significant promise for precise, real-time antibiotic monitoring in critically ill patients.
- This technology can enhance TDM, leading to optimized drug exposure and improved patient outcomes.
- Further development and standardization are necessary for widespread clinical integration.

