4.7 Article

Front-face synchronous fluorescence spectroscopy for rapid and non- destructive determination of free capsanthin, the predominant carotenoid in chili (Capsicum annuum L.) powders based on aggregation- induced emission

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2021.119696

关键词

Capsanthin; Chili powder; Front-face fluorescence spectroscopy; Synchronous fluorescence spectroscopy; Aggregation-induced emission

资金

  1. National Natural Science Foundation of China [21405111]
  2. 131 Second Level Innovative Talents Training Project in Tianjin and Young and Middle-aged Key Innovative Talents Training Project of Tianjin Universities

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The study utilized synchronous front-face fluorescence spectroscopy for rapid and non-invasive detection of free capsanthin in chili powders, revealing two emission mechanisms as AIE and JAF. HPLC was used to determine the content of free capsanthin in 85 chili powder samples, and simple models were established for validation, demonstrating satisfactory analytical results.
Capsanthin is the major natural carotenoid pigment in red chili pepper possessing important bioactivity. Its conventional determination method is high performance liquid chromatography (HPLC) with complex and tedious sample pretreatment. In this study, synchronous front-face fluorescence spectroscopy (FFFS) was applied for the fast and non-invasive detection of free capsanthin in chili powders. Although capsanthin was only weak fluorescent in solution state, it showed strong fluorescence in two separated regions in front-face geometry which could also be clearly observed in chili powders. The mechanisms of these emissions are revealed to be aggregation-induced emission (AIE) and J-aggregate formation (JAF). The free capsanthin in 85 chili powder samples were determined by HPLC as in the range of 0.6-3.0 mg/g. The total synchronous FFFS spectra of these samples were scanned. Simple first-order models were built by partial least square regression (PLSR), and were validated by 5-fold cross-validation and external validation. The coefficients of determination (R-2) were higher than 0.9, and the root mean square errors (RMSE) were less than 0.2 mg/g. The relative error of prediction (REP) was 9.9%, and the residual predictive deviation (RPD) was 3.7. The method was applied for the estimation of free capsanthin in several real-world samples with satisfactory analytical results. The average relative error to HPLC reference values was similar to 11.8%. (C) 2021 Elsevier B.V. All rights reserved.

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