Abstract
A rapid, cost-effective spectrofluorometric method was developed for levothyroxine (T4) detection using fluorescein isothiocyanate (FITC) as a fluorescent probe. The method exploits FITC fluorescence quenching by T4 in Tris/phosphate buffers (pH 7.4),with linear ranges of 8.00 × 10⁻⁶ – 6.40 × 10⁻⁵ mol/L and detection limits of 9.60 × 10⁻⁶ mol/L (Tris) and 8.80 × 10⁻⁶ mol/L (phosphate). Stern-Volmer analysis confirmed dynamic quenching dominated by electrostatic interactions. The method demonstrated 102–104% recovery in spiked human serum and minimal interference from common drugs (Ciprofloxacin, Alendronate) and ions (Fe³⁺, Al³⁺). Compared to HPLC and kinetic methods, this approach offers simplicity, speed, and accessibility for routine pharmaceutical/clinical analysis.