Gingerol, the key bioactive molecule responsible for the pungency and therapeutic benefits of Zingiber officinale (ginger), is an important marker for evaluating the quality and efficacy of herbal and nutraceutical formulations. Variability in natural sources and processing makes its quantitative assessment essential for product standardization. In this short communication, we outline a science-driven HPLC strategy developed for selective and reliable estimation of gingerol in botanical matrices.
Using a reverse-phase chromatographic platform coupled with photodiode array detection, gingerol was effectively resolved from structurally related compounds such as shogaols and paradols, which often interfere in conventional analysis. Calibration using certified reference material demonstrated excellent linearity, ensuring dependable quantification across a practical concentration range. Extracts prepared from raw ginger and commercial herbal formulations produced clean chromatographic profiles with stable retention and high peak purity, confirming the robustness of the approach.
The method supports rapid, reproducible, and regulatorily aligned estimation of gingerol, making it well suited for routine quality control, formulation validation, and authenticity checks in the herbal and nutraceutical sector. This streamlined workflow strengthens scientific confidence in ginger-based products and enhances traceability in natural-product supply chains.
The method enables high-resolution separation of gingerol homologs and degradation products, minimizing matrix interference typical in polyphenolic systems. Retention time consistency and peak purity index confirm method robustness under controlled chromatographic conditions. The approach aligns with regulatory expectations for herbal standardization, providing quantitative authenticity and traceability to manufacturers in the nutraceutical and Ayurvedic sector.


This validated HPLC method supports regulatory compliance, ensures batch consistency, and strengthens MSK’s capability in advanced phytochemical quantification.
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Posted on December 16 2025 By Mitra S.K ADMIN
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