alexa Simultaneous Determination of Asaranin and Sesamin in P
ISSN: 2155-9872

Journal of Analytical & Bioanalytical Techniques
Open Access

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Research Article

Simultaneous Determination of Asaranin and Sesamin in Piper chaba Fruit by using HPTLC-MS Method: Effect of Different Extraction Methods on the Yield of Marker Compounds

Kothapalli Haribabu1, Makula Ajitha2 and Uppuluri Venkata Mallavadhani1*

1Natural Products Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad, India

2Center for Pharmaceutical Sciences, Jawaharlal Nehru Technological University, Hyderabad, India

*Corresponding Author:
Dr. U. V. Mallavadhani
Senior Principal Scientist
Natural Product Chemistry Division
Indian Institute of Chemical Technology [IICT]
Tarnaka, Uppal Road
Hyderabad-607, India
Tel: +91-40-27193167
E-mail: [email protected], [email protected]

Received date: July 04, 2014;Accepted date: August 04, 2014; Published date: August 08, 2014

Citation: Haribabu K, Ajitha M, Mallavadhani UV (2014) Simultaneous Determination of Asaranin and Sesamin in Piper chaba Fruit by using HPTLC-MS Method: Effect of Different Extraction Methods on the Yield of Marker Compounds. J Anal Bioanal Tech 5:199 doi: 10.4172/2155-9872.1000199

Copyright: 2014 Haribabu K, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

A simple, rapid and accurate HPTLC-MS method was developed for the simultaneous quantification of asaranin (AS) and sesamin (SM), the two epimeric furofuran lignans in Piper chaba (Piperaceae) fruit extracts obtained by cold percolation (PER), Soxhlet extraction (SOX), ultrasound assisted extraction (USAE), accelerated solvent extractor (ASE) and microwave assisted extraction (MAE). Separation of AS and SM was achieved on 20×10 cm pre-coated silica gel 60 F254S HPTLC plates with ethyl acetate: hexane (30:70) as mobile phase. Detection and quantification were performed densitometrically at λmax 295 nm. The peak identity was confirmed by electron spray ionization (ESI) mass spectra, which showed the [M + Na]+ ions for both AS and SM at m/z 377. The method was validated according to the ICH guidelines in terms of limit of detection (LOD) and limit of quantification (LOQ), selectivity, linearity, precision, accuracy, and robustness. The results indicate that AS (2.108%) and SM (0.103%) found to present maximum in ASE extract and minimum in PER extract (AS 0.848%; SM 0.048%). By considering the validation results, the method was found to be reproducible and convenient for quantitative analysis of AS and SM in different P. chaba fruit extracts.

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