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    Development and Application of qPCR Assay for Species-specific Identification of Two Animal-derived Tonics: Vinegarquenched Testudinis Carapax et Plastrum and Vinegar-quenched Trionycis Carapax

    Chao Xu1, Xiang Chen2, Jing Han1, Yufei Chen1, Chongyu Ge3, Liwei Wang1, Rong Yang1, Yuping Shen1, Huan Yang1 Corresponding author

    1. 1Department of Chinese Materia Medica and Pharmacy, School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu, People’s Republic of China.
    2. 2Department of Drug Inspection, Zhenjiang Institute for Drug and Food Control, Jiangsu, People’s Republic of China.
    3. 3Department of Pharmacy, Affiliated Hospital of Jiangnan University, 1000 Wuxi, Jiangsu, People’s Republic of China.

    CORRESPONDENCE

    Rong Yang

    Department of Chinese Materia Medica and Pharmacy, School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu, People’s Republic of China.

    syp131@ujs.edu.cn

    Volume 19, Issue 4 · pp. 831–840 · PUBLISHED 2023 · DOI: 10.1177/09731296231188779

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Background: Vinegar-quenched Testudinis Carapax et Plastrum (TCP) and vinegar-quenched Trionycis Carapax (TC) are made from the shells of Chinemys reevesii and Trionyx sinensis. However, some cheap substitutes from non-medicinal species such as Trachemys scripta, Mauremys sinensis, Chelydra serpentina, and Apalone ferox are often seen on the market, which exposes public health to high risk. Conventional methods are not applicable for the identification of these two products since their intrinsic constituents are largely destroyed after being highly processed. Objectives: A new quantitative polymerase chain reaction (qPCR) method was developed to detect DNA components of Vinegar-quenched TCP and vinegar-quenched TC based on simple sequence repeat differential genes of animal-derived mitochondria. Materials and Methods: Six species-specific primer reactions were designed and further validated for specificity, sensitivity, and repeatability. Finally, the developed method was used to assess the authenticity of their commercial products. Results: The assay exhibited good specificity, and the limit of detection was above 1 × 102 copies/µL. There was good linearity in the concentration, ranging from 1 × 102 to 1 × 107 copies/µL. In addition, the method was validated through repeatability assessment (coefficient variation <1%). While qPCR was applied for the analysis of 36 batches of commercial products of these two tonics, it could effectively identify the authenticity of the products, and consequently, seven batches were fake or adulterated. Conclusion: This newly proposed method is promising for the quality evaluation of highly processed animal-derived Chinese medicines, which will assist in ensuring safety and efficacy in clinical practice and protect fair trade in the market.

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      Xu, C., Chen, X., Han, J., Chen, Y., Ge, C., Wang, L., Yang, R., Shen, Y., & Yang, H. (2023). Development and Application of qPCR Assay for Species-specific Identification of Two Animal-derived Tonics: Vinegarquenched Testudinis Carapax et Plastrum and Vinegar-quenched Trionycis Carapax. Pharmacognosy Magazine, 19(4), 831–840. https://doi.org/10.1177/09731296231188779