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Pharmacognostical identification research of Inonotus obliquus

Published on Jul. 31, 2024Total Views: 1171 times Total Downloads: 310 times Download Mobile

Author: ZHU Tianmi 1 DUAN Yuqing 2 WANG Simeng 2 CHEN Shuhe 1 YANG Ying 3 CHEN Keli 2

Affiliation: 1. Department of Pharmacy, Hubei Provincial Hospital of Traditional Chinese Medicine/Affiliated Hospital of Hubei University of Chinese Medicine/Hubei Institute of Traditional Chinese Medicine, Wuhan 430061, China 2. School of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, China 3. Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China

Keywords: Inonotus obliquus Medicinal parts Basal source investigation Trait identification Microscopic identification Molecular biology High-performance liquid chromatography Content determination

DOI: 10.12173/j.issn.1008-049X.202312062

Reference: ZHU Tianmi, DUAN Yuqing, WANG Simeng, CHEN Shuhe, YANG Ying, CHEN Keli.Pharmacognostical identification research of Inonotus obliquus[J].Zhongguo Yaoshi Zazhi,2024, 27(7):1108-1114.DOI: 10.12173/j.issn.1008-049X.202312062.[Article in Chinese]

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Abstract

Objective  To study the identification methods and traits of the Chinese medicinal materials Inonotus obliquus.

Methods  Samples were collected from the origin of northeast China, and source identification, molecular biology identification, trait identification, microscopic identification and HPLC assay were used to study the Inonotus obliquus, its non-pure fungous part, and counterfeit.

Results  Inonotus obliquus had a nodular shape, the microstructure was closely interconnected with mycelia, and the medicinal part was the sclerotium, not the “fruiting body” as stipulated in the current standards of traditional Chinese medicinal materials. Occasionally, a very small amount of tubule and subiculum could be seen in Inonotus obliquus. Tubule hole shape was circular, with a diameter of 130-190 μm, and ruptured. The pipe wall structure was special, which was composed of longitudinal arranged small compartment with diameter of 2-5-8 μm. Non-pure fungous part was the decayed host xylem infiltrated by mycelia. The contents of trametenolic acid and ergosterol in this part were significantly lower than the pure sclerotium (P<0.05). The microstructure and HPLC fingerprints of Inonotus obliquus and the counterfeit burl were clearly distinguishable from each other.

Conclusion   The method used is able to identify the authenticity of Inonotus obliquus and the quality of the medicinal materials.

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References

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