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<p>One of the main objectives of this study is to find an analysis method that has a low environmental and health impact and contributes to achieving sustainability. A simple and sensitive method was established for determination of lacidipine in pure active pharmaceutical ingredient, pharmaceutical formulation and spiked human plasma in presence of its acid induced degradation product. The native emission was measured at 430&#xa0;nm after the excitation at 281&#xa0;nm. A 0.5% Tween-80 solution was used to enhance fluorescence intensity. Peak amplitude of the first derivative synchronous was measured at 409&#xa0;nm by using constant wavelength difference (Δλ = λ<sub>em</sub> - λ<sub>ex</sub> = costant) which equal 160&#xa0;nm. The regression plot of the proposed first derivative synchronous spectrofluorimetric method was found to be linear over the range of 50–300 ng/mL with a determination coefficient equals 0.9997, limit of detection (LOD) was 14.51 ng/mL but limit of quantification (LOQ) was 43.97 ng/mL.</p>

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Green first derivative synchronous spectrofluorimetric determination of lacidipine and its acid degradation product in plasma and mixtures

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年7月17日

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  • Khalid A.M. Attia,
  • Mohamed A. Hasan,
  • Abdalla M. El-Shanawany

摘要

One of the main objectives of this study is to find an analysis method that has a low environmental and health impact and contributes to achieving sustainability. A simple and sensitive method was established for determination of lacidipine in pure active pharmaceutical ingredient, pharmaceutical formulation and spiked human plasma in presence of its acid induced degradation product. The native emission was measured at 430 nm after the excitation at 281 nm. A 0.5% Tween-80 solution was used to enhance fluorescence intensity. Peak amplitude of the first derivative synchronous was measured at 409 nm by using constant wavelength difference (Δλ = λem - λex = costant) which equal 160 nm. The regression plot of the proposed first derivative synchronous spectrofluorimetric method was found to be linear over the range of 50–300 ng/mL with a determination coefficient equals 0.9997, limit of detection (LOD) was 14.51 ng/mL but limit of quantification (LOQ) was 43.97 ng/mL.