基于MGB探针的多液滴数字PCR方法在中药制剂和药材中的种间鉴定。

IF 6.7 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2025-01-01 DOI:10.1016/j.phymed.2024.156325
Kai-Ling Xu , Zhong-Mou Zhang , Ya-Dan Wang , Xian-Long Cheng , Hong-Yu Jin , Feng Wei , Shuang-Cheng Ma
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引用次数: 0

摘要

背景:液滴数字聚合酶链反应(ddPCR)由于具有较高的灵敏度和绝对定量能力,被广泛应用于病毒和细菌的检测。然而,利用ddPCR技术鉴定中药和中成药原植物种类的研究很少。目的:探讨采用ddPCR技术鉴别切牙白杨和猪头白杨的可行性,为中药材和制剂的质量控制建立一种灵敏、定量的方法。方法:基于稳定的单核苷酸多态性设计特异性的MGB探针和引物。根据多重PCR和qPCR的结果,设计并优化了ddPCR的实验条件,最终确定了方法的检出限(LOD)和定量限(LOQ)。并对市场上流通的九味强活丸中附子的原植物种类进行了鉴定。结果:多重PCR和qPCR结果表明探针和引物具有特异性。通过Qsep分析和Sanger测序,确定了切齿奈瑟菌和franchetii奈瑟菌的特异性扩增产物分别为283和206 bp。优化后的ddPCR体系测得的定量限分别为0.000816 ng/µl,切齿乳杆菌和凤尾乳杆菌的定量限分别为0.00408和0.003312 ng/µl。此外,对四种九味强活丸中的白芍进行了扩增,并采用ddPCR方法成功鉴定。结论:本研究建立了一种MGB探针多重ddPCR方法,可用于白芍的鉴别和定量,为多源中草药的鉴定和定量提供了基础。
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MGB probe-based multiplex droplet digital PCR for the interspecific identification of Notopterygii Rhizoma et Radix in herbal materials and preparations

Background

Owing to high sensitivity and ability for absolute quantification, the droplet digital polymerase chain reaction (ddPCR) is widely used for viral and bacterial detection. However, few studies have been conducted on the application of ddPCR to identify the original plant species used in traditional Chinese medicine and Chinese patent medicine.

Purpose

In this study, we investigated the feasibility of using ddPCR to differentiate between Notopterygium incisum and N. franchetii to establish a sensitive and quantitative method for quality control of herbal materials and preparations.

Methods

Specific minor groove binding (MGB) probes and primers were designed based on stable single nucleotide polymorphisms. The ddPCR experimental conditions were designed and optimised according to the results of multiplex PCR and qPCR, which ultimately confirmed the limits of detection and quantification (LOD and LOQ, respectively) of the method for Notopterygii Rhizoma et Radix. Additionally, the original plant species of Notopterygii Rhizoma et Radix in Jiuwei Qianghuo pills circulating in the market were identified.

Results

The results of the multiplex PCR and qPCR indicated that the probes and primers were specific. Furthermore, a Qsep analyser and Sanger sequencing were used to confirm that the specific amplification products of N. incisum and N. franchetii were 283 and 206 bp, respectively. The optimised ddPCR system was employed to determine the LOD to be 0.000816 ng/µl, and LOQ of N. incisum and N. franchetii to be 0.00408 and 0.003312 ng/µl, respectively. In addition, Notopterygii Rhizoma et Radix in four Jiuwei Qianghuo pills was amplified and successfully identified using ddPCR assays.

Conclusion

This study established a multiplex ddPCR method using MGB probes to identify Notopterygii Rhizoma et Radix, providing a foundation for the identification and quantification of multi-source Chinese herbal medicines.
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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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