Aishwary Awasthi, Aradhana Tripathi, Shristi Sharma, Aparna Tiwari, Chhavi Baran, Sweta Sharma, K N Uttam
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引用次数: 0
Abstract
The accurate monitoring of the fruit ripening is crucial for maintaining quality and prevention from post-harvest economic losses. Goldenberry, being rich in vitamins, minerals, and carotenoids, yet its ripening assessment relies on variable and often subjective traditional approaches. To address this, the present study utilises rapid and non-destructive techniques using confocal micro-Raman and UV-Vis spectroscopy to track biochemical changes in both the exocarp and mesocarp of goldenberry fruit across five ripening stages: pre-mature, mature, pre-ripe, ripe, and post-ripe. The analysis of Raman spectra of exocarp shows an increase in carotenoid bands up to ripe stage, followed by a decrease at post-ripe stage, while the mesocarp exhibits a continuous increase in carotenoid intensity through stage post-ripe. The UV-Vis spectral analysis supports these observations, indicating increasing carotenoid content alongside a reduction in chlorophyll as ripening progresses. Among different machine learning (ML) approaches, unsupervised clustering demonstrates strong performance of k-means and agglomerative nesting, with high rand index values (>0.97). In supervised domain, support vector machine, logistic regression, random forest, decision tree, and principal component-linear discriminant analysis achieves the highest values of performance metrices including accuracy, precision, recall, F1 score, ROC/AUC values, and cross validation scores. Moreover, partial least squares regression analysis demonstrates excellent predictive power, with R2 = 0.93 (calibration) and 0.70 (cross-validation) for exocarp and R2 = 0.91 (calibration) and 0.89 (cross-validation) for mesocarp. The combined use of Raman with ML enables a practical and reliable framework for assessing fruit ripening, with promising applications in quality control and post-harvest management.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.