VALIDATION OF NEW LIQUID CHROMATOGRAPHIC METHOD FOR NATURALLY ISOLATED QUERCETIN AND ITS COMMERCIAL APPLICATION TO AYURVEDIC FORMULATION

Author:

Dinnimath B. M,Jalalpure S. S.,

Abstract

Quercetin was isolated from Aerva lanata (L) and investigated for method development. A simple, accu- rate, reproducible method was developed using RP-HPLC. Commercial formulation of Quercetin 250mg capsules (Quercetin Complex-Solgar, USA) was used followed by an Ayurvedic proprietary medicine for the study. The chromatographic separation was performed on Shiseido Capcell Pak C 18 column (250 X 4.6 mm, 5 μm), mobile phase developed was 0.3% formic acid:acetonitrile:methanol (40:20:40) at the flow rate of 10μL/min at 22 0 C. The detector used was PDA with the detection wavelength of 370 nm. R T was 4.9mn with LOD-0.816 μg/ml and LOQ-2.473 μg/ml. The correlation coefficient was 0.992%. The linearity range was observed in the concentration range of 2-20 μg/mL and the recovery was found to be 99.91 to 102.65 %. Finally, the method applied to KACHCHNAR Ayurvedic formulation justified with characteristic peak for identifying quercetin in it.

Publisher

Indian Drug Manufacturers' Association (IDMA)

Subject

Drug Discovery,Pharmaceutical Science,Pharmacology

Reference23 articles.

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3. [3] Vijaya S.K ., Vijaya R.J., Annapurna A., Ravikumar B.V.V.: Reversed-Phase HPLC Method for Determination of Quercetin in Human Plasma. Asian J. Chem. 2009; 21, 101-04.

4. [4] WHO. Quality Control Methods for Medicinal Plant Material. WHO/PHARM, Geneva: WHO/PHARM; 1992. p. S. 559.

5. [5] Breaux J, Kevin J and Boulas P. Analytical Methods Development and Validation. Pharmaceutical Technology and Analytical Chemistry & Testing. 2003; p. 6.

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