ArticleFrontiers in pharmacology2026
Establishing a TaqMan qPCR method for identification and quantification of
Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Methods: A highly specific TaqMan real-time quantitative polymerase chain reaction (qPCR) method was established to identify HBBM from ZBM based on the 47 bp amplicon located on the internal transcribed spacer region of the nuclear ribosomal DNA. Results: The qPCR assay developed herein could specifically distinguish ZBM from HBBM. The sensitivity study showed that the detectable DNA template concentration of HBBM for this assay was 0.001 ng/μL. The efficiency of the optimized qPCR assay was evaluated to be 90.2% (R Conclusion: The TaqMan real-time qPCR assay developed in this study has high efficiency, sensitivity, and specificity; this method is applicable for not only authentication of ZBM and HBBM but also quantitative detection of a binary mixture or adulterated botanical drugs. Furthermore, it provides a reference for qualitative control of other traditional Chinese medicines.
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