2018
DOI: 10.1007/s40290-018-0252-8
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Adulterants and Contaminants in Psychotropic Herbal Medicines Detected with Mass Spectrometry and Next-Generation DNA Sequencing

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Cited by 16 publications
(11 citation statements)
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“…Next-Generation Sequencing (NGS) technologies have been applied to herbal drug authentication using genome skimming or amplicon metabaroding approaches [ 1 , 8 , 87 , 88 , 89 , 90 , 91 , 92 ], including H. perforatum commercial products [ 16 ]. The quality of a herbal product is determined by the correct identity of its ingredients and its purity, measured by % contamination by a range of inorganic and biological contaminants.…”
Section: Discussionmentioning
confidence: 99%
“…Next-Generation Sequencing (NGS) technologies have been applied to herbal drug authentication using genome skimming or amplicon metabaroding approaches [ 1 , 8 , 87 , 88 , 89 , 90 , 91 , 92 ], including H. perforatum commercial products [ 16 ]. The quality of a herbal product is determined by the correct identity of its ingredients and its purity, measured by % contamination by a range of inorganic and biological contaminants.…”
Section: Discussionmentioning
confidence: 99%
“…As it was previously reported by many peer-reviewed reports (Hoban et al, 2018;Seethapathy et al, 2019;Amritha et al, 2020;Anthoons et al, 2021;Palhares et al, 2021), irrespective of the authentication method, adulterated commercial HPs are geographically present across all continents (Supplementary Table S1). Moreover, this highly relevant category of commercial products was found to not comply with the labeled botanical ingredients in proportions almost identical (26 ± 2%), irrespective if they are traditionally used as herbal medicines, as commonly found in Asia, or overwhelmingly consumed as food supplements as in Europe or North America.…”
Section: Discussionmentioning
confidence: 53%
“…Previously described in [12,17], fusion primers with unique 6-8 bp multiplex identifier (MID) tags were designed for the same plant and mammal primer sets as used for the qPCR above, but with the inclusion of a second chloroplast gene region, rbcL (see Coghlan et al [12] for primer details). Fusion tag PCR was carried out using the same cycling conditions, with duplicate reactions for each DNA extract.…”
Section: Amplicon Generationmentioning
confidence: 99%
“…The data analysis has been previously described in [12,17]. The sequencing output files were retrieved, filtered and processed using Geneious (v8.1).…”
Section: Bioinformatic Analysismentioning
confidence: 99%