Related Experiment Video
Updated: May 10, 2026

Construction of Models for Nondestructive Prediction of Ingredient Contents in Blueberries by Near-infrared Spectroscopy Based on HPLC Measurements
Published on: June 28, 2016
Quantification of anthocyanins in Oryza sativa L. from Jammu and Kashmir, India by a validated high performance thin
Soibam Tampha1, Robinson C Jose1, Sushil Kumar Chaudhary2
1BRIC-Institute of Bioresources and Sustainable Development (Department of Biotechnology, Government of India), Takyelpat, Imphal 795001, Manipur, India.
Abstract:
Anthocyanins are bioactive compounds with antioxidant, anti-obesity, and anti-inflammatory properties beneficial for human health. HPTLC is an effective technique that is ideal for analysing both qualitatively and quantitatively. One of the advantages of HPTLC over HPLC (High performance liquid chromatography) and LC-MS (Liquid chromatography mass spectrometry) is the capability to analyse crude samples consisting of various compounds along with the capacity to apply multiple samples and a range of standards on a single plate with enhanced accuracy and precision of quantification without constrains of time. This study aimed to develop and validate a high performance thin-layer chromatography (HPTLC) method for the identification and quantification of anthocyanins in Oryza sativa L. methanolic extracts collected from the Jammu and Kashmir region of India. Pre-coated TLC plates (20 × 10 cm) with silica gel 60F254 as the stationary phase, and the mobile phase consisted of ethyl acetate: 2-butanol: formic acid: water (9:6:3:3, v/v/v/v) were used. Major anthocyanins peonidin-3-O-glucoside chloride, cyanidin-3-glucoside chloride, peonidin-3-glucoside chloride and kuromanin were identified in Black rice and Mushk Budji rice. Cyanidin-3,5-diglucoside chloride was detected exclusively in Black rice. Densitometric evaluation was performed at 520-540 nm. Method validation adhered to ICH guidelines, demonstrating specificity, linearity (r²: 0.9992-0.9999), precision (RSD < 2 %), and robustness. The limit of detection (LOD) and quantitation (LOQ) ranged from 7.57 to 36.08 ng/band and 12.96 to 61.79 ng/band, respectively. This validated method provides a reliable approach for detecting adulteration and ensuring the quality control of anthocyanin-rich raw materials used in food and nutraceutical products.
More Related Videos
10:09A Straightforward Method for Glucosinolate Extraction and Analysis with High-pressure Liquid Chromatography (HPLC)
Published on: March 15, 2017
10:22Improved UPLC-UV Method for the Quantification of Vitamin C in Lettuce Varieties (Lactuca sativa L.) and Crop Wild Relatives (Lactuca spp.)
Published on: June 30, 2020
Related Concept Videos
Thin-Layer Chromatography (TLC): Overview
To begin the analysis, a mixture of compounds is spotted on the starting line on the TLC plate using a thin capillary. The bottom of the...
Principles Of Column Chromatography