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DETERMINATION OF RELATIVE FLUORESCENCE QUANTUM YIELD USING THE AGILENT CARY ECLIPSE

Applications | 2016 | Agilent TechnologiesInstrumentation
Fluorescence spectroscopy
Industries
Food & Agriculture
Manufacturer
Agilent Technologies

Summary

Importance of the Topic


The fluorescence quantum yield is a fundamental parameter in analytical chemistry, representing the efficiency of photon emission relative to absorption. In food dye analysis, reliable quantum yield measurements support product quality assessment, regulatory compliance, and formulation optimization.

Objectives and Study Overview


This study demonstrates a comparative approach to determine the relative fluorescence quantum yield of food dyes by benchmarking against curcumin, a reference fluorophore with a known yield. Two dye batches are evaluated to illustrate method performance and product quality differentiation.

Methodology and Instrumentation


Analytical approach:
  • Comparative method based on plotting integrated fluorescence area versus absorbance for both reference and sample.
  • Quantum yield calculation via Q = Q_r × (m/m_r) × (n²/n_r²), where m and m_r are calibration slopes and n, n_r are solvent refractive indices.

Instrument setup:
  • Agilent Cary Eclipse fluorescence spectrometer for emission spectra (420–421 nm excitation for curcumin; 449–450 nm for food dyes).
  • Agilent Cary 60 UV-Vis spectrometer for precise absorbance measurements.
  • Parameters: 10 mm pathlength cuvettes, data acquisition up to 80 points / s, full spectral scans in <3 s.

Sample preparation:
  • Curcumin standards (absorbance 0.01–0.1 AU at 420–421 nm).
  • Food dye solutions in dimethylformamide (DMF) with similar absorbance range and matched excitation regions.
  • Integration of emission spectra (425–600 nm for curcumin; 455–600 nm for dyes) via WinFL software.

Main Results and Discussion


Calibration curves exhibited excellent linearity for curcumin and two food dye batches. Using curcumin’s literature quantum yield (0.174 in acetone) and refractive indices (DMF = 1.43; acetone = 1.36), calculated yields were:
  • Batch 1: Q = 0.70
  • Batch 2: Q = 0.67
Key considerations include matching excitation/emission ranges between reference and sample, maintaining absorbance within 0.01–0.1 AU, and accurate refractive index values.

Benefits and Practical Applications


The comparative method offers higher accuracy and reproducibility compared to single-point approaches. Measured quantum yields serve as quality metrics in dye manufacturing, enable batch-to-batch consistency checks, and support R&D in formulation development and stability studies.

Future Trends and Potential Applications


Emerging developments may include:
  • Automated high-throughput workflows integrating UV-Vis and fluorescence measurements.
  • Use of novel reference standards with extended spectral coverage.
  • Real-time, in-line monitoring of fluorescent properties during production.
  • Advanced time-resolved fluorescence techniques to probe dynamic processes in complex matrices.

Conclusion


This work validates a robust comparative protocol using the Agilent Cary Eclipse and Cary 60 systems to determine relative fluorescence quantum yields. The approach reliably differentiates dye batches, providing essential data for quality control and product development.

References


1. Joseph R. Lakowicz, Principles of Fluorescence Spectroscopy, 3rd Edition, Springer Science, 2006.

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