UV Method Development and Validation of Ellagic Acid for its Rapid Quantitative Estimation
Abstract
Development and validation of a simple UV- Spectroscopy method was done for the quantitative analysis of Ellagic Acid (EA). The stock solution of 50μg/ml was prepared and scanned, for which absorption maxima was found to be 277nm. Further dilutions to different concentrations (1-5μg/ml) were prepared and analyzed at 277nm. The method so developed was validated as per ICH guidelines for: linearity, robustness, precision, accuracy, limit of detection and quantification. The Lambert- Beer’s law is followed in the range (1-5μg/ml) with correlation coefficient value 0.9994. It was observed that the method is precise and accurate for EA analysis with good recovery percent of 94.47% to 106.83%. The method developed was further employed for determining the entrapment efficiency of ellagic acid and its release from its nanoparticle dosage form. The method may be utilized for determining the concentration of EA when present as formulation and in combination with other drugs.
- Page Number : 01-05
- Keywords
UV-Spectroscopy, Validation, Ellagic Acid, Correlation Coefficient, Precision, Robustness - DOI Number
https://doi.org/10.15415/jptrm.2019.71001 -
Authors
- Harsheen Kaur Amity Institute of Pharmacy, Amity University, Noida, UP- 201303, India.
- Arti Thakkar Amity Institute of Pharmacy, Amity University, Noida, UP- 201303, India.
- Kalpana Nagpal Amity Institute of Pharmacy, Amity University, Noida, UP- 201303, India.
References
- ICH (2005) Q2 (R1), Validation of Analytical Procedures: Text and Methodology, ICH Harmonized Tripartite Guidelines, 2005.
- Avachat A.M. and Patel V.G.(2015). Self nano emulsifying drug delivery system of stabilized ellagic acid-phospholipid complex with improved dissolution and permeability. Saudi Pharm J., 23, 276–289. https://doi.org/10.1016/j.jsps.2014.11.001
- Shah, M. A., Patel, H. and Raj, H. (2017). Methods for the estimation of Ellagic Acid and Curcumin in Antidiabetic Herbal Formulations - A Review. Eurasian J. Anal. Chem., 12, 295–311.https://doi.org/10.12973/ejac.2017.00171a
- Mady, F. M. and Shaker, M. A. (2017). Enhanced anticancer activity and oral bioavailability of ellagic acid through encapsulation in biodegradable polymeric nanoparticles. Int. J. Nanomedicine, 12, 7405–7417. https://doi.org/10.2147/IJN.S147740
- Bala, I., Bhardwaj, V., Hariharan, S. and Kumar, M. N. (2006). Analytical methods for assay of ellagic acid and its solubility studies. J. Pharm. Biomed. Anal, 40,206–210.https://doi.org/10.1016/j.jpba.2005.07.006
- Zhou, T., Xiao, X., Li, G. and Cai, Z. W. (2011). Study of polyethylene glycol as a green solvent in the microwave-assisted extraction of flavone and coumarin compounds from medicinal plants. J. Chromatogr. A, 1218, 3608-3615. https://doi.org/10.1016/j.chroma.2011.04.031
- Chen Jia-hong, Wu Dong-mei, Wang Yong-mei, et al. (2007). Study on Quantitative Determination of Ellagic Acid by UV-spectrophotometry. Biomass Chemical Engineering, 41, 18–20
- Tiwari, G. and Tiwari, R. (2010). Bioanalytical method validation: An updated review. Pharmaceutical Methods, 1(1), 25–38.https://doi.org/10.1016/S2229-4708(10)11004-8
- Behera, S., Ghanty, S., Ahmad, F., Santra, S. and Banerjee, S. (2012). UV-Visible Spectrophotometric Method Development and validation ofAssay of Paracetamol Tablet Formulation. J. Anal. Bioanal. Techniques, 3, 151.https://doi.org/10.4172/2155-9872.1000151
- Khanage, S.G., Mohite, P.B. and Jhadav S. (2013) Development and Validation of UV-Visible Spectrophotometric Method for Simultaneous Determination of Eperisone and Paracetamol in Solid Dosage Form. Adv. Pharm. Bull, 3, 447–451.
- Gopalakrishnan, L., Ramana, L. N., Sethuraman, S. and Krishnan, U. M. (2014). Ellagic Acid Encapsulated Chitosan Nanoparticles as Anti-hemorrhagic Agent. Carbohydr Polym., 111, 215–221.https://doi.org/10.1016/j.carbpol.2014.03.093
- Nagpal, K., Singh, S.K. and Mishra, D.N. (2012). Nanoparticle mediated brain targeted delivery of gallic acid: in vivo behavioural and biochemical studies for improved antioxidant and antidepressant-like activity. Drug Deliv., 19, 378–391.https://doi.org/10.3109/10717544.2012.738437
- Sharma, A., Thavathiru, E., Benbrook, D. M. and Woo, S. (2017). Bioanalytical method development and validation of HPLCUV assay for the quantification of SHetA2 in mouse and human plasma: Application to pharmacokinetics study. J. Pharm. Technol. Drug Res., 6. https://doi.org/10.7243/2050-120X-6-2
- Bostijn, N., Hellings, M., Veen, M. V. D., Vervaet, C. and Beer, T. D. (2018). In-line UV spectroscopy for the quantification of low-dose active ingredients during the manufacturingof pharmaceuticalsemi-solid and liquid formulations. Anal. Chim. Acta, 1013, 54–62. https://doi.org/10.1016/j.aca.2018.02.007
Published Date : 2019-05-10