4.6 Article

Real-Time,Seconds-Resolved Measurements of Plasma Methotrexate In Situ in the Living Body

期刊

ACS SENSORS
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.2c01894

关键词

biosensors; methotrexate; aptamers; drug monitoring; electrochemical sensors

资金

  1. NIH [EB022015]
  2. European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curi [799332]
  3. Fondazione Umberto Veronesi postdoctoral Fellowship [0001420]
  4. Otis Williams Postdoctoral Fellowship
  5. Marie Curie Actions (MSCA) [799332] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

This study develops an electrochemical aptamer-based (EAB) sensor for real-time monitoring of drug levels in the living body. The sensor has wide applicability and high precision with seconds-resolved measurements.
Dose-limiting toxicity and significant patient-to-patient pharmacokinetic variability often render it difficult to achieve the safe and effective dosing of drugs. This is further compounded by the slow, cumbersome nature of the analytical methods used to monitor patient-specific pharmacokinetics, which inevitably rely on blood draws followed by post-facto laboratory analysis. Motivated by the pressing need for improved therapeutic drug monitoring, we are developing electrochemical aptamer-based (EAB) sensors, a minimally invasive biosensor architecture that can provide real-time, seconds-resolved measurements of drug levels in situ in the living body. A key advantage of EAB sensors is that they are generalizable to the detection of a wide range of therapeutic agents because they are independent of the chemical or enzymatic reactivity of their targets. Three of the four therapeutic drug classes that have, to date, been shown measurable using in vivo EAB sensors, however, bind to nucleic acids as part of their mode of action, leaving open questions regarding the extent to which the approach can be generalized to therapeutics that do not. Here, we demonstrate real-time, in vivo measurements of plasma methotrexate, an antimetabolite (a mode of action not reliant on DNA binding) chemotherapeutic, following human-relevant dosing in a live rat animal model. By providing hundreds of drug concentration values, the resulting seconds-resolved measurements succeed in defining key pharmacokinetic parameters, including the drug's elimination rate, peak plasma concentration, and exposure (area under the curve), with unprecedented 5 to 10% precision. With this level of precision, we easily identify significant (>2-fold) differences in drug exposure occurring between even healthy rats given the same mass-adjusted methotrexate dose. By providing a real-time, seconds-resolved window into methotrexate pharmacokinetics, such measurements can be used to precisely individualize the dosing of this significantly toxic yet vitally important chemotherapeutic.

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