4.6 Article

Quantification of Methotrexate in Human Serum Using Surface-Enhanced Raman Scattering-Toward Therapeutic Drug Monitoring

期刊

ACS SENSORS
卷 6, 期 7, 页码 2664-2673

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.1c00643

关键词

surface-enhanced Raman scattering; therapeutic drug monitoring; quantitative SERS; methotrexate; point-of-care detection; patient samples

资金

  1. Danish National Research Foundation [DNRF122]
  2. Villum Fonden [9301]
  3. BioInnovation Institute Foundation for Therapeutic Drug Monitoring [NNF20SA0063552]
  4. Danish Cancer Society [R257-A14720]
  5. Danish Childhood Cancer Foundation [2019-5934, 2020-6759]

向作者/读者索取更多资源

Therapeutic drug monitoring (TDM) is crucial for drugs with pharmacokinetic variability and a narrow therapeutic window. Monitoring MTX is essential for determining drug clearance rate and administering rescue drug to prevent toxicity and death. The developed NPAS method enables fast and accurate quantification of MTX from human serum, showing potential for TDM in clinical settings.
Therapeutic drug monitoring (TDM) can improve clinical care when using drugs with pharmacokinetic variability and a narrow therapeutic window. Rapid, reliable, and easy-to-use detection methods are required in order to decrease the time of analysis and can also enable TDM in resource-limited settings or even at bedside. Monitoring methotrexate (MTX), an anticancer drug, is critical since it is needed to follow the drug clearance rate and decide how to administer the rescue drug, leucovorin (LV), in order to avoid toxicity and even death. We show that with the optimized nanopillar-assisted separation (NPAS) method using surface-enhanced Raman scattering, we were able to measure MTX in PBS and serum in the linear range of 5-150 mu M and confirmed that MTX detection can be carried out even in the presence of LV. Additionally, when NPAS was combined with centrifugal filtration, a quantification limit of 2.1 mu M for MTX in human serum sample was achieved. The developed detection method enables fast detection (10 min) and quantification of MTX from human serum (>90% accuracy). Furthermore, we show the potential of the developed method for TDM, when quantifying MTX from clinical samples, collected from patients who are undergoing high-dose MTX therapy.

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