Development and validation of new spectroscopic method for the estimation of furazolidone in bulk and solid dosage form

D.S. Mittan, P. Kumar, S.P. Venkatesh Prasad, L. Kumar, S. Kumar

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

A simple and sensitive spectroscopic method in ultraviolet region was developed and validated for the estimation of Furazolidone in pure and pharmaceutical dosage forms. The method is based on Furazolidone, showing absorbance at 259 nm for zero order derivative spectroscopy respectively in acetonitrile and distilled water. This method obey's Beers law in the concentration range of 2 to 18 ug/ml respectively. The proposed method is precise, accurate, linear, stable and reproducible and can be extended to the analysis of furazolidone in bulk and tablet formulations.
Original languageEnglish
Pages (from-to)1009-1012
Number of pages4
JournalOriental Journal of Chemistry
Volume24
Issue number3
Publication statusPublished - 2008
Externally publishedYes

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Furazolidone
Dosage Forms
Tablets
absorbance
Spectroscopy
Derivatives
Spectrum Analysis
drug
Water
spectroscopy
Pharmaceutical Preparations
method
dosage
water

Cite this

Mittan, D. S., Kumar, P., Venkatesh Prasad, S. P., Kumar, L., & Kumar, S. (2008). Development and validation of new spectroscopic method for the estimation of furazolidone in bulk and solid dosage form. Oriental Journal of Chemistry, 24(3), 1009-1012.
Mittan, D.S. ; Kumar, P. ; Venkatesh Prasad, S.P. ; Kumar, L. ; Kumar, S. / Development and validation of new spectroscopic method for the estimation of furazolidone in bulk and solid dosage form. In: Oriental Journal of Chemistry. 2008 ; Vol. 24, No. 3. pp. 1009-1012.
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abstract = "A simple and sensitive spectroscopic method in ultraviolet region was developed and validated for the estimation of Furazolidone in pure and pharmaceutical dosage forms. The method is based on Furazolidone, showing absorbance at 259 nm for zero order derivative spectroscopy respectively in acetonitrile and distilled water. This method obey's Beers law in the concentration range of 2 to 18 ug/ml respectively. The proposed method is precise, accurate, linear, stable and reproducible and can be extended to the analysis of furazolidone in bulk and tablet formulations.",
author = "D.S. Mittan and P. Kumar and {Venkatesh Prasad}, S.P. and L. Kumar and S. Kumar",
note = "Cited By :1 Export Date: 10 November 2017 Correspondence Address: Mittan, D.S.; Department of Pharmaceutical Analysis, PES College of Pharmacy, Bangalore, India References: Martindale. The complete drug reference: Published by Pharmaceutical Press, 34th edition; 605 (2005); Drug Profile of Furazolidone (www.drug.com, www.wikipedia.com); Howden, A., In vitro sensitivity of Campylobacter pyloridis to furazolidone (1986) Lancet, 2, p. 1035; Mahedro, M.C., Diaz Galeano, T., Pascual Galeno, S., (2002) J Pharm, Biomed Anal, 29 (3), pp. 477-485; Prasad, C.V.N., Sripriya, V., Saha, R.N., Parimoo, S., (1999) J Pharm Biomed Anal, 21 (5), pp. 961-968; Loppez-de-alba, P.L., Wrobel, K., Lopez-Martinez, L., Wrobel, K., Yepez- Murrieta, L., Amador-Hernandez, J., (1997) J Pharm Biomed Anal, 16, pp. 349-355",
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Mittan, DS, Kumar, P, Venkatesh Prasad, SP, Kumar, L & Kumar, S 2008, 'Development and validation of new spectroscopic method for the estimation of furazolidone in bulk and solid dosage form', Oriental Journal of Chemistry, vol. 24, no. 3, pp. 1009-1012.

Development and validation of new spectroscopic method for the estimation of furazolidone in bulk and solid dosage form. / Mittan, D.S.; Kumar, P.; Venkatesh Prasad, S.P.; Kumar, L.; Kumar, S.

In: Oriental Journal of Chemistry, Vol. 24, No. 3, 2008, p. 1009-1012.

Research output: Contribution to journalArticle

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T1 - Development and validation of new spectroscopic method for the estimation of furazolidone in bulk and solid dosage form

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AU - Kumar, P.

AU - Venkatesh Prasad, S.P.

AU - Kumar, L.

AU - Kumar, S.

N1 - Cited By :1 Export Date: 10 November 2017 Correspondence Address: Mittan, D.S.; Department of Pharmaceutical Analysis, PES College of Pharmacy, Bangalore, India References: Martindale. The complete drug reference: Published by Pharmaceutical Press, 34th edition; 605 (2005); Drug Profile of Furazolidone (www.drug.com, www.wikipedia.com); Howden, A., In vitro sensitivity of Campylobacter pyloridis to furazolidone (1986) Lancet, 2, p. 1035; Mahedro, M.C., Diaz Galeano, T., Pascual Galeno, S., (2002) J Pharm, Biomed Anal, 29 (3), pp. 477-485; Prasad, C.V.N., Sripriya, V., Saha, R.N., Parimoo, S., (1999) J Pharm Biomed Anal, 21 (5), pp. 961-968; Loppez-de-alba, P.L., Wrobel, K., Lopez-Martinez, L., Wrobel, K., Yepez- Murrieta, L., Amador-Hernandez, J., (1997) J Pharm Biomed Anal, 16, pp. 349-355

PY - 2008

Y1 - 2008

N2 - A simple and sensitive spectroscopic method in ultraviolet region was developed and validated for the estimation of Furazolidone in pure and pharmaceutical dosage forms. The method is based on Furazolidone, showing absorbance at 259 nm for zero order derivative spectroscopy respectively in acetonitrile and distilled water. This method obey's Beers law in the concentration range of 2 to 18 ug/ml respectively. The proposed method is precise, accurate, linear, stable and reproducible and can be extended to the analysis of furazolidone in bulk and tablet formulations.

AB - A simple and sensitive spectroscopic method in ultraviolet region was developed and validated for the estimation of Furazolidone in pure and pharmaceutical dosage forms. The method is based on Furazolidone, showing absorbance at 259 nm for zero order derivative spectroscopy respectively in acetonitrile and distilled water. This method obey's Beers law in the concentration range of 2 to 18 ug/ml respectively. The proposed method is precise, accurate, linear, stable and reproducible and can be extended to the analysis of furazolidone in bulk and tablet formulations.

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