Evidence map›Paper›PMID 37658082›Full record

ArticleScientific reports2023

Application of a modified tetra-primer ARMS-PCR assay for rapid Panax species identity authentication in ginseng products.

Zhengxiu Yang, Yat Tung Lo, Zheng Quan, Junchen He, Yanjun Chen, Adam Faller, Tiffany Chua, Hoi Yan Wu, Yanjun Zhang, Qiang Zou and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Zhengxiu Yang *Quality Control Laboratory, Herbalife NatSource (Hunan) Natural Products Co., Changsha, 410100, China.
Yat Tung Lo *Li Dak Sum Yip Yio Chin R & D Centre for Chinese Medicine, State Key Laboratory of Research on Bioactivities and Clinical Applications of Medicinal Plants (CUHK) and School of Life Sciences, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
Zheng QuanCorporate Center of Excellence Quality Laboratory, Herbalife International of America, Inc., 950 W 190th Street, Torrance, CA, 90502, USA.
Junchen HeQuality Control Laboratory, Herbalife NatSource (Hunan) Natural Products Co., Changsha, 410100, China.
Yanjun ChenQuality Control Laboratory, Herbalife NatSource (Hunan) Natural Products Co., Changsha, 410100, China.
Adam FallerCorporate Center of Excellence Quality Laboratory, Herbalife International of America, Inc., 950 W 190th Street, Torrance, CA, 90502, USA.
Tiffany ChuaHerbalife International of America, Inc., Corporate Quality, 990 W 190th Street, Torrance, CA, 90502, USA.
Hoi Yan WuLi Dak Sum Yip Yio Chin R & D Centre for Chinese Medicine, State Key Laboratory of Research on Bioactivities and Clinical Applications of Medicinal Plants (CUHK) and School of Life Sciences, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
Yanjun ZhangHerbalife International of America, Inc., Corporate Quality, 990 W 190th Street, Torrance, CA, 90502, USA.
Qiang ZouQuality Control Laboratory, Herbalife NatSource (Hunan) Natural Products Co., Changsha, 410100, China.
Fan LiQuality Control Laboratory, Herbalife NatSource (Hunan) Natural Products Co., Changsha, 410100, China.
Peter ChangHerbalife International of America, Inc., Corporate Quality, 990 W 190th Street, Torrance, CA, 90502, USA.
Gary SwansonHerbalife International of America, Inc., Corporate Quality, 990 W 190th Street, Torrance, CA, 90502, USA.
Pang Chui ShawLi Dak Sum Yip Yio Chin R & D Centre for Chinese Medicine, State Key Laboratory of Research on Bioactivities and Clinical Applications of Medicinal Plants (CUHK) and School of Life Sciences, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China. pcshaw@cuhk.edu.hk.
Zhengfei LuCorporate Center of Excellence Quality Laboratory, Herbalife International of America, Inc., 950 W 190th Street, Torrance, CA, 90502, USA. zhengfeil@herbalife.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Panax ginseng products can be adulterated with materials from other Panax species. The purpose of this study is to provide a rapid P. ginseng authentication method for simultaneous identification of P. ginseng and detection of adulteration in ginseng products at different processing stages. First, a tetra-primer ARMS-PCR assay was designed based on a single-nucleotide polymorphism (SNP) within the trnL-trnF region and was tested at 28 PCR cycles with DNA extracted from Botanical Reference Materials (BRMs). Next, 5' end random nucleotide and 3' terminus phosphorothioates linkage modifications were incorporated into the inner primers to improve sensitivity and specificity at 40 PCR cycles. Finally, the modified assay was validated using characterized market ginseng materials and the detection limit was determined. The modified tetra-primer ARMS-PCR assay can achieve the desired sensitivity and specificity using one set of reaction conditions in ginseng materials at different stages. In validation, it was able to correctly identify target species P. ginseng and differentiate it from closely related species. This study suggests that the modified tetra-primer ARMS-PCR assay can be used for the rapid, species identity authentication of P. ginseng material in ginseng products. This assay can be used to complement chemical analytical methods in quality control, so both species identity and processing attributes of ginseng products can be efficiently addressed.

Indexed as

PanaxBiological AssayDrug ContaminationNucleotidesPolymerase Chain ReactionNucleotides

Identifiers

PMID37658082
PMCPMC10474259

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.