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Development, Assessment, Improvement, and Standardization of Methods in Herbal Drug Research

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Editorial16 November 2022
Editorial: Development, assessment, improvement, and standardization of methods in herbal drug research

HD, therefore, the quality assurance and the authenticity of HD must be assured (Heinrich, 2015). The complexity of herbs and extracts from different sources of HD, typically consisting of many constituents, has raised major quality issues. The bioactive compounds of extracts and/or HD preparation is typically very complex, and may vary, if the exact chemical composition is not determined accurately and specifically, the reported bioactivity or pharmacological effects may not always be reproducible. The assurance of high-quality HD with reproducible quality, acceptable, good efficacy, and safe from herbal drugs is a challenging task. As a consequence, the availability of appropriate analytical methods is highly required not only for their identification and standardization, but also for the detection of adulterants and contaminants (Muyumba et al., 2021). The analytical methods either chemical or biological-based methods used for quality controls of HD must be official methods, otherwise, the methods should first be validated according to the latest official guidelines. Without analytical method validation, the reliability of the data cannot be confirmed, and the results cannot be replicated by other scientists (Indrayanto, 2022).The quality control and authentication of HD are typically carried out by evaluating the characteristics of biological and physicochemical properties along with microscopic and macroscopic observations. The characterization and discrimination of HD performed using instrumental analyses can use three approaches, namely (1) single component analysis or targeted analysis by investigating along with identification and quantitative analysis of marker compounds which are responsible to certain biological activities, (2) fingerprinting profiling by comparing the profiles of different HD, and (3) metabolomic studies either using targeted or untargeted metabolomics (Ruiz et al., 2016). Due to large datasets obtained during quality control of HD using these instruments, the use of chemometrics is a must. Pattern recognition and multivariate calibration are among chemometrics techniques widely used in analysis of HD (Zhu et al., 2014). and processed Fuzi, herbal medicine used for the treatment of various diseases. Forty two metabolic markers were identified to discriminate raw and steamed-processed Fuzi. Six alkaloids, namely mesaconitine, aconitine, hypaconitine, benzoylmesaconine, benzoylaconine, and benzoylhypaconine can be used as markers for differentiation pof raw and processed Fuzi. DESI-MSI combined with metabolomics provides an efficient method to visualize the changeable rules and screen the metabolic markers of Aconitum alkaloids during processing.Overall, three approaches (single component analysis, metabolic fingerprinting and metabolomics studies) have been used by authors to discover chemical markers which are related to biological activities as well as identification, differentiation and classification of HD.

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2 citations

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Herbal drugs or herbal medicines (HMs) have a long-standing history as natural remedies for preventing and curing diseases. HMs have garnered greater interest during the past decades due to their broad, synergistic actions on the physiological systems and relatively lower incidence of adverse events, compared to synthetic drugs. However, assuring reproducible quality, efficacy, and safety from herbal drugs remains a challenging task. HMs typically consist of many constituents whose presence and quantity may vary among different sources of materials. Fingerprint analysis has emerged as a very useful technique to assess the quality of herbal drug materials and formulations for establishing standardized herbal products. Rather than using a single or two marker(s), fingerprinting techniques take great consideration on the complexity of herbal drugs by evaluating the whole chemical profile and extracting a common pattern to be set as a criterion for assessing the individual material or formulation. In this review, we will describe and assess various fingerprinting techniques reported to date which are applicable to herbal drug standardization and quality control. We will also evaluate the application of multivariate data analysis or chemometrics in assisting the analysis of the complex datasets from the determination of HMs. To ensure that these methods yield reliable results, we will review the validation status of the methods and provide perspectives on those. Finally, we will conclude by highlighting major accomplishments and presenting a gap analysis between the existing techniques and what is needed to continue moving forward.

28,837 views

232 citations

ORIGINAL RESEARCH
9 March 2022
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27 citations

ORIGINAL RESEARCH
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ORIGINAL RESEARCH
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