<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tao Y</submitter><funding>Key Project of Regulatory Science Research of Anhui Drug Administration</funding><funding>the National Key Research and Development Program of China</funding><funding>NIFDC Fund for Key Technology Research</funding><funding>Key Project of NMPA Scientific System Construction for Drug Regulation</funding><pagination>3763</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12472803</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(18)</volume><pubmed_abstract>Due to morphological similarities, adulterants are frequently substituted for Qingfengteng (QFT, &lt;i>Sinomenium acutum&lt;/i>) in regional markets. This study developed a TaqMan probe-based real-time quantitative polymerase chain reaction (qPCR) assay targeting a 57-base pair (bp) fragment of the internal transcribed spacer 2 (ITS2) region for the specific detection of QFT. The method was validated using a diverse set of samples, including: (1) 19 batches of QFT and 8 batches of Beidougen (BDG, &lt;i>Menispermum dauricum&lt;/i>), comprising both medicinal materials and decoction pieces; (2) 5 batches each of decoction pieces from Qingsheteng (QST, &lt;i>Periploca calophylla&lt;/i>), Jishiteng (JST, &lt;i>Paederia foetida&lt;/i>), Kuanjinteng (KJT, &lt;i>Tinospora sinensis&lt;/i>), and Huibeiqingfengteng (HBQFT, &lt;i>Sa</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Development of TaqMan Real-Time Fluorescent Quantitative PCR Method for Identification and Quantification of &amp;lt;i&amp;gt;Sinomenium acutum-&amp;lt;/i&amp;gt;Originated Herbal Drugs.</pubmed_title><pmcid>PMC12472803</pmcid><funding_grant_id>NMPAJGKX-2024</funding_grant_id><funding_grant_id>AHYJ-KJ-202402</funding_grant_id><funding_grant_id>2023YFC3504104</funding_grant_id><funding_grant_id>GJJS-2022-7-2</funding_grant_id><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Tao Y</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Wei F</pubmed_authors><pubmed_authors>Duan S</pubmed_authors><pubmed_authors>Yu K</pubmed_authors><pubmed_authors>Cheng X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of TaqMan Real-Time Fluorescent Quantitative PCR Method for Identification and Quantification of &amp;lt;i&amp;gt;Sinomenium acutum-&amp;lt;/i&amp;gt;Originated Herbal Drugs.</name><description>Due to morphological similarities, adulterants are frequently substituted for Qingfengteng (QFT, &lt;i>Sinomenium acutum&lt;/i>) in regional markets. This study developed a TaqMan probe-based real-time quantitative polymerase chain reaction (qPCR) assay targeting a 57-base pair (bp) fragment of the internal transcribed spacer 2 (ITS2) region for the specific detection of QFT. The method was validated using a diverse set of samples, including: (1) 19 batches of QFT and 8 batches of Beidougen (BDG, &lt;i>Menispermum dauricum&lt;/i>), comprising both medicinal materials and decoction pieces; (2) 5 batches each of decoction pieces from Qingsheteng (QST, &lt;i>Periploca calophylla&lt;/i>), Jishiteng (JST, &lt;i>Paederia foetida&lt;/i>), Kuanjinteng (KJT, &lt;i>Tinospora sinensis&lt;/i>), and Huibeiqingfengteng (HBQFT, &lt;i>Sa</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-02T03:12:18.657Z</modification><creation>2026-05-02T03:08:09.416Z</creation></dates><accession>S-EPMC12472803</accession><cross_references><pubmed>41011655</pubmed><doi>10.3390/molecules30183763</doi></cross_references></HashMap>