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UV-Visible spectrophotometry of Repaglinide in bulk and in formulation by using methyl orange as reagents | ||
Journal of the Iranian Chemical Research | ||
مقاله 1، دوره 4، شماره 2، شهریور 2011، صفحه 69-76 اصل مقاله (128.84 K) | ||
نویسندگان | ||
Smita Sharma* 1؛ Mukesh Chandra Sharma2 | ||
1Department of Chemistry Chodhary Dilip Singh Kanya Mahavidyalya Bhind (M.P) 477001, India | ||
2School of Pharmacy, Devi Ahilya Vishwavidyalaya, Indore (M.P)-452001, India | ||
چکیده | ||
Two sensitive spectrophotometric methods are presented for the assay of Repaglinide in bulk drug and in formulations using methyl orange, as reagents. Oxidant by reacting with a fixed amount of either methyl orange and measuring the absorbance at 485.2 nm (method-I) and measuring the absorbance at 618.9 nm (method-II). Developed method is based on the formation of extractable colored complex of drug with coloring agent Methyl orange dye. A wavelength maximum was found to be 618.9 nm. The concentration range of 15-50 μg ml-1 with linear regression of 0.9995, while the percentage recovery, LOD and LOQ were 99.42-99.08 %, 2.17 μg ml-1 and 1.08 μg ml-1 respectively. The result of analysis have been validated statistically and also by recovery studies. From the percentage recovery and specificity studies it was concluded that there was no interference of common additives during the estimation. This proves the suitability of this method for the routine quality control analysis of the Repaglinide in formulation. | ||
کلیدواژهها | ||
Repaglinide؛ Derivative spectrophotometry؛ Area under curve | ||
مراجع | ||
[1] M.D.Rockville, United States Pharmacopoeia; 25th (Eds) United States Pharmacopoeial Convention Inc, (2002) 2150. [2] S.Budavari, the Merck Index. 13th (eds) Whitehouse Station (NJ, USA) Merck and Co Inc (2001) 790. [3] J.E.F Reynolds, Martindale, 33 rd ed. (London), the Complete Drug Reference Pharmaceutical Press, (2002) 334. [4] M.D. Rockville, United State Pharmacopoeia, (Asian Eds) USP Convention Inc, (2003) 623. [5] A.B. Ruzilawati, M.S. Wahab, A. Imran, Z. Ismail, S.H. Gan, J. Pharm. Biomed. Anal. 43 (2007) 1831-1835. [6] M. Gandhimathi, T.K. Ravi, S.K. Renu, Anal. Sci. 19 (2002) 1675-1677. [7] R.H. Khan, S. Talegaonkar, R.M. Singh, S.C. Mathur, R. Shiv, G.N. Singh, Indian Drugs 44 (2007) 428-433. [8] A. Gumieniczek, A. Berecka, H. Hopkała, J. Planar Chromatogr. 18 (2005) 155-159. Parameters Repaglinide Method I Method II Working λ (nm) 485.2 nm 618.9 nm Beer’s law limit (μg mL-1) 5-35 5-35 5-35 0-45 Correlation coefficient * 0.9965 0.9994 0.9998 0.9999 Intercept * 0.0003 0.0014 0.0043 0.0021 Slope * 0.0143 0.0221 0.0651 0.0765 Limit of detection, μg mL-1 2.17 -0.74 Limit of quantification, μg mL-1 1.08 0.18 S. Sharma & M.Ch. Sharma / J. Iran. Chem. Res. 4 (2011) 69-76 76 [9] A. Goyal, I. Singhvi, Indian. J. Pharm. Sci. 68 (2006) 656-657. [10] ICH, Stability Testing of New Drug Substances and Products, in: Proceeding of the International Conference on Harmonisation, IFPMA, Geneva, (2003). [11] M. Bakshi, S. Singh, J. Pharm. Biomed. Anal. 28 (2003) 1011-1040. [12] A.B. Thomas, M.R. Patankar, K.R. Deshmukh, L.P. Kothapalli, S.J. Jangam, S.H. Bodkhe, A.D. Deshpande, Indian Drugs 44 (2007) 745-750. [13] S.B. Chepurwar, A.A. Shirkhedkar, S.B. Bari, S.J. Surana, S.J. Indian Drugs 43 (2006) 803-806 [14] A.G. Davison, A.H. Beckette, J.B. Stenlake, Practical Pharmaceutical Chemistry, CBS Publishers and distributors, New Delhi.275 (1997). | ||
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