@article {1342, title = {High-Performance Thin Layer Chromatography Methods for Estimation of Chemical Markers in Stachytarpheta indica Vahl.}, journal = {Pharmacognosy Research}, volume = {17}, year = {2025}, month = {January 2025}, pages = {94-99}, type = {Original Article}, chapter = {94}, abstract = {

Background: Stachytarpheta indica Vahl. (Verbenaceae family), commonly known as Indian Snakeweed, is a valuable medicinal plant. A systematic phytochemical analysis of bioactives of this plant is lacking till date. Objectives: The present study is aimed to develop validated High-Performance Thin-Layer Chromatography (HPTLC) methods for quantification of 6 marker compounds, β-sitosterol, lupeol, ursolic acid, apigenin, caffeic acid and verbascoside in S. indica plant. Materials and Methods: Normal phase chromatography was used to develop mobile phase systems that could aid in the identification and quantification of the phytochemicals in the entire plant. Several enhancements were made to the basic method of thin-layer chromatography to automate the different steps, to increase the resolution achieved and to allow more accurate quantitative measurement. The methods were validated as per the International Council for Harmonization (ICH) guidelines. Results: The linear regression analysis data for the calibration plots showed a good linear relationship (r2=0.9873-0.9979) in the concentration range of 1-5 μg for β-sitosterol, lupeol and ursolic acid; 0.5-5 μg for apigenin, 1-3 μg for caffeic acid; and 3-8 μg per spot for verbascoside with respect to area. The average recoveries for phytoconstituents were 98.32 to 98.97\%, indicating the good reproducibility. Verbascoside 1.3598{\textpm}0.014\% w/w was present at high concentration and ursolic acid 0.0027{\textpm}0.0007\% w/w was present at low concentration in the whole plant powder. Conclusion: The validated TLC-densitometric methods were simple, precise, accurate, specific and can be used for the routine quality control of raw materials of S. indica.

}, keywords = {Apigenin, Caffeic acid, High-performance thin-layer chromatography, Stachytarpheta indica, Ursolic acid, Verbascoside}, doi = {10.5530/pres.20251934}, author = {Vihangi Patel and Krupa Gadhvi and Karuna Modi and Mamta Shah} } @article {407, title = {Development of Validated High-performance Thin-layer Chromatography Method for Simultaneous Determination of Quercetin and Kaempferol in Thespesia populnea}, journal = {Pharmacognosy Research}, volume = {9}, year = {2017}, month = {July 2017}, pages = {277-281}, type = {Original Article}, chapter = {277}, abstract = {

Introduction: Thespesia populnea L. (Family: Malvaceae) is a well-known medicinal plant distributed in tropical regions of the world and cultivated in South Gujarat and indicated to be useful in cutaneous affections, psoriasis, ringworm, and eczema. Bark and fruits are indicated in the diseases of skin, urethritis, and gonorrhea. The juice of fruits is employed in treating certain hepatic diseases. The plant is reported to contain flavonoids, quercetin, kaempferol, gossypetin, Kaempferol-3-monoglucoside, β-sitosterol, kaempferol-7-glucoside, and gossypol. T. populnea is a common component of many herbal and Ayurvedic formulation such as Kamilari and Liv-52. Objective: The present study aimed at developing validated and reliable high-performance thin layer chromatography (HPTLC) method for the analysis of quercetin and kaempferol simultaneously in T. populnea. Method: The method employed thin-layer chromatography aluminum sheets precoated with silica gel as the stationary phase and toluene: ethyl acetate: formic acid (6:4:0.3 v/v/v) as the mobile phase, which gave compact bands of quercetin and kaempferol. Result: Linear regression data for the calibration curves of standard quercetin and kaempferol showed a good linear relationship over a concentration range of 100{\textendash}600 ng/spot and 500{\textendash}3000 ng/spot with respect to the area and correlation coefficient (R2) was 0.9955 and 0.9967. The method was evaluated regarding accuracy, precision, selectivity, and robustness. Limits of detection and quantitation were recorded as 32.06 and 85.33 ng/spot and 74.055 and 243.72 ng/spot for quercetin and kaempferol, respectively. Conclusion: We concluded that this method employing HPTLC in the quantitative determination of quercetin and kaempferol is efficient, simple, accurate, and validated.

}, keywords = {High-performance thin-layer chromatography, Kaempferol, Quercetin, Thespesia populnea}, doi = {10.4103/0974-8490.210326}, author = {Hiteksha Panchal and Aeshna Amin and Mamta Shah} }