Detection of Adulteration in Herbal Formulation Containing Phyllanthus emblica Terminalia bellirica and Terminalia chebula using DNA Based Approach

dc.contributor.guideDr. Preetam P Joshi
dc.coverage.spatial
dc.creator.researcherTravadi Tasnim Hunedbhai
dc.date.accessioned2025-09-01T06:07:05Z
dc.date.available2025-09-01T06:07:05Z
dc.date.awarded2024
dc.date.completed2024
dc.date.registered2019
dc.description.abstractThe increasing global demand for herbal medicines and dietary supplements, while offering potential health benefits, has also raised concerns about product quality and authenticity. Herbal products, often derived from traditional knowledge and practices, are susceptible to adulteration due to factors like species similarity and the surge in demand for specific therapeutic properties. This study focuses on three traditionally and economically important medicinal species, Terminalia bellirica (TB), Terminalia chebula (TC), and Phyllanthus emblica (PE), known for their therapeutic benefits and often subjected to adulteration. DNA-based methods tend to be more reliable, accurate and cost-effective for authentication. The isolating of high-quality amplifiable DNA from these plant species, especially in processed products, remains challenging. This is primarily due to the presence of polyphenols, which interfere with DNA extraction and amplification. To address this, the study developed an optimized DNA isolation protocol. This protocol incorporated specific buffer modifications to stabilize pH during extraction and introduced polyvinylpyrrolidone as a phenolic compound scavenger to minimize interference during cell lysis. The effectiveness of this optimized protocol was evaluated using the species-specific ITS-based SCAR markers, digital PCR and ITS2 metabarcode on six of each Baheda (TB fruit), Harde (TC fruit), Amala (PE fruits) and Triphala (containing three fruits of TB, TC, and PE) market formulation. Results demonstrated a significant improvement in DNA quality and quantity, leading to successful species identification. Furthermore, the study employed digital PCR (dPCR) to enhance sensitivity, achieving a two-fold increase compared to conventional PCR. This marks the first reported instance of a dPCR application for authenticating TB, TC, and PE. This research underscores the critical role of optimized DNA isolation protocols in ensuring the quality and authenticity of herbal products.
dc.description.note
dc.format.accompanyingmaterialCD
dc.format.dimensions134
dc.format.extentA4
dc.identifier.researcherid
dc.identifier.urihttp://hdl.handle.net/10603/660476
dc.languageEnglish
dc.publisher.institutionBiotechnology
dc.publisher.placeRajkot
dc.publisher.universityAtmiya University
dc.relation230
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordBiotechnology and Applied Microbiology
dc.subject.keywordLife Sciences
dc.subject.keywordMicrobiology
dc.titleDetection of Adulteration in Herbal Formulation Containing Phyllanthus emblica Terminalia bellirica and Terminalia chebula using DNA Based Approach
dc.title.alternative
dc.type.degreePh.D.

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