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Field Identification of Matricaria chamomilla using a Portable qPCR System
Published on: October 10, 2020
A streamlined analytical strategy combining plant metabolomics and interpretable machine learning for detecting
Hongxu Zhou1, Yi Zhang2, Jingyi Yan3
1Chongqing Key Laboratory of New Drug Screening from Traditional Chinese Medicine, Integrative Science Center of Germplasm Creation in Western China (Chongqing) Science City and Southwest University, SWU-TAAHC Medicinal Plant Joint R&D Centre, College of Pharmaceutical Sciences, Southwest University, Chongqing, China; CQMPA Key Laboratory for Quality Control and Evaluation of Traditional Chinese Medicine, Chongqing Institute for Food and Drug Control, Chongqing, China.
Abstract:
Panax notoginseng powder (PNP) is a high-value traditional Chinese medicine, yet persistent supply shortages have increased the risk of economically motivated adulteration. The covert homologous adulteration of PNP with its non-medicinal fibrous roots (FR) presents a formidable analytical bottleneck due to highly overlapping chemical profiles, leaving a critical gap in quality regulation. This study aimed to develop a highly accurate, interpretable, and deployable analytical strategy for homologous adulterant detection. Herein, we propose an integrated analytical approach combining LC-MS-based untargeted and targeted metabolomics, explainable machine learning (ML), and SHAP-guided feature selection to overcome the intractable challenge of authenticating PNP against homologous FR adulteration. Among the five ML models, XGBoost achieved the highest accuracy, with 100% accuracy for adulteration types. The SHAP analysis identified five quality markers (Q-markers), and a novel XGBoost model achieved 100% accuracy in classifying the Adulterated PNP category. Furthermore, notoginsenoside Fd (N-Fd) was biologically validated as an ecologically stress-driven defense biomarker uniquely enriched in FR. Application of the model to 84 commercial PNP and Hongyaopian samples identified a subset of products with FR-like ginsenoside profiles, highlighting its potential utility as a preliminary risk-screening tool for market surveillance. By conquering this ultimate homologous adulteration challenge, this computationally lightweight and interpretable paradigm establishes a cost-effective, modernized standard for routine industrial botanical quality control.
