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Dual-Quenching Mechanism-Based Fluorometric Sensing Platform for Precise D-Penicillamine Quantification in
Yousef A Bin Jardan1, Mohamed M El-Wekil2, Aya M Mostafa2
1Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, 11451, Saudi Arabia.
Journal of Fluorescence
|April 7, 2025
Summary
A new fluorometric method uses red carbon dots and cobalt ions to detect D-penicillamine (D-PA). This sensitive D-PA detection is crucial for therapeutic drug monitoring and understanding drug behavior in different health conditions.
Area of Science:
- Analytical Chemistry
- Biomedical Engineering
- Materials Science
Background:
- D-penicillamine (D-PA) is vital for treating Wilson's disease, rheumatoid arthritis, and heavy metal poisoning.
- Precise D-PA quantification is essential due to its narrow therapeutic window and toxicity.
- Current detection methods may lack the sensitivity required for effective therapeutic drug monitoring.
Purpose of the Study:
- To develop a novel, highly sensitive fluorometric method for D-penicillamine detection.
- To establish a sophisticated sensing platform for enhanced analytical performance.
- To validate the method for therapeutic drug monitoring in biological samples.
Main Methods:
- Utilized red-emissive carbon dots (R@CDs) and cobalt ions for a novel sensing platform.
- Employed a dual-quenching mechanism involving competitive displacement and inner filter effects.
- Validated the method using rat plasma samples from healthy and diabetic models.
Main Results:
- Achieved excellent linearity (R² = 0.9971) and an ultra-low limit of detection (0.0041 µM).
- Successfully quantified D-PA in rat plasma, demonstrating applicability in therapeutic drug monitoring.
- Revealed variations in D-PA pharmacokinetics between healthy and diabetic rats.
Conclusions:
- The developed fluorometric method offers high sensitivity and reliability for D-PA detection.
- This method has significant potential for personalized therapeutic drug monitoring.
- Findings contribute to a better understanding of D-PA disposition in different physiological states.

