Introduction: Derris elliptica (Wall.) Benth. (Leguminosae) is the tropical plant which has been used as natural poison as well as veterinary medicine due to its best-known phytochemical compound, rotenone to kill invertebrates and fish. However, there is no report on pharmacognostic specification and quantification of rotenone content from D. elliptica stems. Objective: This present study aimed to conduct the pharmacognostic parameters as well as to conduct the validated methods to quantify rotenone content in D. elliptica stems following WHO guideline. Methods: Dried D. elliptica stems from 15 different areas in Thailand were examined for pharmacognostic secification. Their rotenone contents were quantitatively analyzed by TLC densitometry using winCATS software as well as TLC-image analysis using ImageJ free software. Results: Macroscopic and microscopic characteristics, TLC fingerprint and physicochemical parameters were reported in this study. The water content, loss on drying, total ash content and acidinsoluble ash content were determined to be 8.81±1.30, 5.77 ±0.92, 7.35±0.63, 1.221±0.20%, respectively. The ethanol, and water-soluble extractive values were found to be 4.07±1.23 and 11.31±1.68%, respectively. Additionally, the validation method for quantification of rotenone content was developed. The contents of rotenone in D. elliptica stem ethanolic extract evaluated by TLC-densitometry and TLC-image analysis were found to be 0.2870±0.1242 and 0.2844±0.1209% by dried weight, respectively. The result between these two analytical methods were shown no significant difference. Conclusion: The validated methods were able to effectively quantify rotenone content in D. elliptica stems from various locations in Thailand which could be used for the specification of this raw material with reference to its chemical marker. Thus, this study provides the necessary and adequate information for authentication and standardization of D. elliptica stems.
The study aimed to evaluate pharmacognostic parameters for standardization of raw materials, Thunbergia laurifolia Lindl. (family: Thunbergiaceae) stems and leaves, as well as their active phytochemical (rosmarinic acid) contents. The antidiabetic potential was evaluated by yeast α-glucosidase inhibitory activity using p-nitrophenyl-α-D-glucopyranoside as substrate. Dried stems and leaves of Thunbergia laurifolia were collected from 15 different locations in Thailand. The microscopic anatomical and histological characteristics of stem and leaf were illustrated. The physico-chemical contents, including loss on drying, acid-insoluble ash, total ash, ethanol-soluble extractives, water-soluble extractives, and moisture of dried stems and leaves, were established. TLC-densitometry of rosmarinic acid in dried T. laurifolia stems and leaves were developed and revealed contents of 0.120 ± 0.079 and 0.291 ± 0.150 g per 100 g, respectively. Similarly, TLC-image analysis by ImageJ showed contents of 0.127 ± 0.094 and 0.303 ± 0.162 g per 100 g respectively (p > 0.05). Both quantitative TLC demonstrated their validity due to specificity, accuracy, repeatability, intermediate precision, limit of detection, limit of quantitation, and robustness. The antidiabetic potential of rosmarinic acid, T. laurifolia leaf and stem ethanolic extracts, and acarbose (positive control) exhibited IC50 of 0.31, 0.80, 5.89, and 1.48 mg/ml, respectively.
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