Development of a fluorescent nano-sensing probe for atomoxetine analysis: Additional clinical pharmacokinetic study.

Spectrochim Acta A Mol Biomol Spectrosc

Department of Pharmaceutical Chemistry, College of Pharmacy, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia; Addiction and Neuroscience Research Unit, Health Science Campus, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia. Electronic address:

Published: December 2024

AI Article Synopsis

  • Atomoxetine is a psychostimulant used to treat ADHD symptoms in individuals with autism, and eco-friendly carbon quantum dots (CQDs) were created to help quantify this drug in pharmaceutical capsules and human plasma.
  • The CQDs' selectivity for atomoxetine improved through functionalization, and their quantification involved measuring fluorescence quenching, revealing a dynamic mechanism of interaction.
  • The method developed was validated and showed strong performance in clinical studies, indicating effective atomoxetine absorption and a favorable ecological impact based on greenness evaluation metrics.

Article Abstract

Atomoxetine is a psychostimulant drug used for the treatment of attention-deficit/hyperactivity disorder (ADHD) symptoms in people with autism. Herein, eco-friendly fluorescent carbon quantum dots (CQDs) were synthesized using black-eyed pea beans and characterized for the purpose of quantifying atomoxetine in pharmaceutical capsules and human plasma. The selectivity of these CQDs towards atomoxetine was improved by functionalizing their surface with an atomoxetine-tetraphenylborate ion complex. The quantification of atomoxetine is based on measuring the fluorescence quenching of the functionalized CQDs in response to varying concentrations of atomoxetine. The Stern-Volmer plot was employed to investigate the mechanism through which atomoxetine quenches the fluorescence intensity of the CQDs. The outcomes indicated a dynamic quenching mechanism. The applied method was optimized and validated in compliance with ICH requirements, resulting in excellent linearity across the concentration range of 50-800 ng/mL. The developed method was successfully used to quantify atomoxetine in pharmaceutical dosage form and human plasma with acceptable accuracy and precision outcomes. In addition, the method was applied for clinical pharmacokinetic study of atomoxetine in the plasma of children diagnosed with both autism and ADHD. Atomoxetine was rapidly absorbed after a single oral dose of 10 mg, reaching maximum concentration within two hours and having a half-life (t) of 3.11 h. Moreover, the method demonstrates a notable degree of eco-friendliness, as evidenced by two greenness evaluation metrics; Green Analytical Procedure Index (GAPI) and Analytical GREEnness (AGREE).

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.saa.2024.124793DOI Listing

Publication Analysis

Top Keywords

atomoxetine
10
clinical pharmacokinetic
8
pharmacokinetic study
8
study atomoxetine
8
atomoxetine pharmaceutical
8
human plasma
8
development fluorescent
4
fluorescent nano-sensing
4
nano-sensing probe
4
probe atomoxetine
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!