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Pharmaceuticals (Basel, Switzerland)
2021
March
27;
14
(4)
:297
Comprehensive and Rapid Quality Evaluation Method for the Ayurvedic Medicine Divya-Swasari-Vati Using Two Analytical Techniques: UPLC/QToF MS and HPLC-DAD
Acharya Balkrishna (1)
,
Acharya Balkrishna (1)
,
Sudeep Verma (1)
,
Sudeep Verma (1)
,
Priyanka Sharma (1)
,
Priyanka Sharma (1)
,
Meenu Tomer (2)
,
Meenu Tomer (2)
,
Jyotish Srivastava (2)
,
Jyotish Srivastava (2)
,
Anurag Varshney (1)
,
Anurag Varshney (1)
,
Acharya Balkrishna (3)
,
Acharya Balkrishna (3)
,
Anurag Varshney (3)
,
Anurag Varshney (3)
1. Drug Discovery and Development Division, Patanjali Research Institute, Haridwar 249 405, Uttarakhand, India 2. Drug Discovery and Development Division, Patanjali Research Institute, Haridwar 249 405, Uttarakhand, India 3. Department of Allied and Applied Sciences, University of Patanjali, Haridwar 249 405, Uttarakhand, India.
Abstract
Divya-Swasari-Vati (DSV) is a calcium-containing herbal medicine formulated for the symptomatic control of respiratory illnesses observed in the current COVID-19 pandemic. DSV is an Ayurvedic medicine used for the treatment of chronic cough and inflammation. The formulation has shown its pharmacological effects against SARS-CoV-2 induced inflammation in the humanized zebrafish model. The present inventive research aimed to establish comprehensive quality parameters of the DSV formulation using validated chromatographic analytical tools. Exhaustive identification of signature marker compounds present in the plant ingredients was carried out using ultra performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC/QToF MS). This was followed by simultaneous estimation of selected marker components using rapid and reliable high-performance liquid chromatography (HPLC) analysis. Eleven marker components, namely gallic acid, protocatechuic acid, methyl gallate, ellagic acid, coumarin, cinnamic acid, glycyrrhizin, eugenol, 6-gingerol, piperine and glabridin, were selected out of seventy-four identified makers for the quantitative analysis in DSV formulation. Validation of the HPLC method was evaluated by its linearity, precision, and accuracy tests as per the International Council of Harmonization (ICH) guidelines. Calibration curves for the eleven marker compounds showed good linear regression (r2 > 0.999). The relative standard deviation (RSD) value of intraday and interday precision tests were within the prescribed limits. The accuracy test results ranged from 92.75% to 100.13%. Thus, the present inclusive approach is first of its kind employing multi-chromatographic platforms for identification and quantification of the marker components in DSV, which could be applied for routine standardization of DSV and other related formulations. Keywords: Ayurveda; Divya-Swasari-Vati; HPLC; UPLC/QToF MS; herbal medicine; validation.
DHARA ID:
D059308
Pubmed ID:
33801579
Link To Full Paper
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