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Year : 2010  |  Volume : 72  |  Issue : 4  |  Page : 508-510
Simultaneous estimation of metformin and pioglitazone by ultraviolet spectrophotometry


1 Department of Pharmacy, G. R. D. Institute of Management and Technology, 214-Rajpur Road, Dehradun-248 009, India
2 Department of Pharmacy, Abhilashi College of Pharmacy, Mandi-175 008, India

Date of Submission07-Sep-2009
Date of Decision08-Mar-2010
Date of Acceptance04-Aug-2010
Date of Web Publication14-Dec-2010

Correspondence Address:
Laxmi Goswami
Department of Pharmacy, G. R. D. Institute of Management and Technology, 214-Rajpur Road, Dehradun-248 009
India
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DOI: 10.4103/0250-474X.73940

PMID: 21218066

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   Abstract 

This work deals with the simultaneous estimation of metformin hydrochloride and pioglitazone hydrochloride in a bilayered tablet dosage form, without prior separation by two techniques. The methods employed are derivative spectrophotometery and Q analysis. The absorption maxima at 231 nm and 269 nm were used for the estimation of metformin and pioglitazone, respectively. Both the drugs and their mixture obey Beer-Lamberts law at selected wavelength at given concentration range. The result of analysis has been validated statistically and recovery studies confirmed the accuracy of the proposed method. The proposed procedures are simple, rapid, require no separation steps and can be used for the routine analysis of both drugs.


Keywords: Derivative spectrophotometery, metformin, pioglitazone, q-analysis, simultaneous equation method


How to cite this article:
Goswami L, Mukhopadhyay S, Durgapal S. Simultaneous estimation of metformin and pioglitazone by ultraviolet spectrophotometry. Indian J Pharm Sci 2010;72:508-10

How to cite this URL:
Goswami L, Mukhopadhyay S, Durgapal S. Simultaneous estimation of metformin and pioglitazone by ultraviolet spectrophotometry. Indian J Pharm Sci [serial online] 2010 [cited 2014 Apr 24];72:508-10. Available from: http://www.ijpsonline.com/text.asp?2010/72/4/508/73940


Combined tablets of metformin and pioglitazone hydrochloride are available containing 500 mg of metformin and 15 mg of pioglitazone hydrochloride. Because metformin's insulin-sensitizing effect occurs mainly at the liver, combination with thiazolidinediones (TZDs), which mainly sensitize muscle to insulin-mediated glucose uptake, is a rational therapeutic strategy [1] .

The aim of this paper was to explore the possibility of using techniques of absorbance ratio or Q-analysis method and derivative spectrophotometery methods for quantifying metformin and pioglitazone simultaneously in their mixture form. The advantage of these proposed methods is that no separation is required. The proposed procedures are simple, rapid and act as convenient alternative to HPLC method [2] .

The absorption spectra of the reference and test solutions were recorded over the range of 200-400 nm keeping the solutions in 1 cm quartz cells using Shimadzu UV/Vis double beam spectrophotometer model 1700 Pharmaspec.

Gift samples of pure metformin and pioglitazone hydrochloride were procured from Zydus Cadila, Sikkim. Combined metformin and pioglitazone tablets (Pioz*MF-15 containing metformin-500 mg and pioglitazone-15 mg and manufactured by USV Limited) were purchased from a local pharmacy. Analytical reagent grade hydrochloric acid, N,N-dimethyl formamide, distilled water was used as solvent. Stock solutions (500 μg/ml) of metformin and pioglitazone hydrochloride were prepared by dissolving separately 50 mg in 10 ml of N,N-dimethyl formamide in 100 ml volumetric flasks, and the volume was made up to 100 ml with 0.1 N hydrochloric acid.

In the quantitative assay of two components by Q-analysis method [3] , absorbance were measured at two wavelengths, one being the isoabsorptive point and other being the wavelength of maximum absorption of one of the two components. From the overlain spectra of metformin and pioglitazone, 247.5 nm was the isoabsorptive point for both the drugs and other at 231 nm, the λmax for metformin was selected [Figure 1]. The method employs Q-values, concentrations of drugs in sample solutions were determined using equation C 1 = (Q 0 -Q 2 )/(Q 1 -Q 2 )×(A/a 1 ) for pioglitazone and C 2 = (Q 0 -Q 2 )/(Q 2 -Q 1 )×(A/a 2 ) for metformin, where Q 0 = absorption of sample at 231 nm/absorption of sample at 247.5 nm, Q 1 = absorptivity of pioglitazone at 231 nm/absorptivity of pioglitazone at 247.5 nm, Q 2 = absorptivity of metformin at 231 nm/absorptivity of metformin at 247.5 nm, A= absorption of sample at isoabsorptive point and a 1 and a 2 = absorptivities of pioglitazone and metformin respectively at isoabsorptive point.
Figure 1: Overlain Spectra of metformin and pioglitazone

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In the derivative spectrophotometery [4] method solutions of 10 μg/ml of metformin and pioglitazone were prepared separately. Both the solutions were scanned in the spectrum mode from 400 to 200 nm. The absorption spectra thus obtained were derivatized from first to fourth order. First order derivative was selected for analysis of both the drugs. The zero crossing wavelengths, 269 and 231 nm were selected for pioglitazone and metformin respectively [Figure 2].
Figure 2: Derivative spectrophotometry of metformin and pioglitazone

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For preparation of calibration curves five mixed standards having concentrations 0.5, 1, 1.5, 3 and 4.5 μg/ml of pioglitazone and 16.5, 33, 50, 100 and 150 μg/ml of metformin, respectively were prepared and scanned in the spectrum mode from 400 to 200 nm. The absorption spectra so obtained were derivatized to obtain first derivative order spectra. The absorbance of pioglitazone and metformin were measured at 269 and 231 nm, respectively and working calibration curves of both the drugs were plotted separately. The concentration of individual drug present in the mixture was determined against calibration curve in quantitation mode.

Twenty tablets were weighed accurately. The average weight was determined and then ground to a fine powder. A quantity equivalent to 15 mg of pioglitazone and 500 mg of metformin were transferred to a 100 ml volumetric flask. The contents were ultrasonicated for 10 min with solvent, made to volume and filtered through Whatmann filter paper. The solution was further diluted with solvent, to give concentration of μg/ml of pioglitazone and metformin, respectively. Absorbance of these solutions was measured at 269 nm and 231 nm, and concentration of pioglitazone and metformin obtained from standard calibration curve. Results of tablet analysis of the tablet formulation are reported in [Table 1]. Accuracy, reproducibility and precision of the proposed method were studied with the help of recovery studies that was carried out by addition of standard drug solution to pre-analyzed sample.
Table 1: Analysis of Tablet Formulation

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The proposed methods for simultaneous estimation of pioglitazone and metformin dosage forms were found to be simple, accurate, economical and rapid. In both the methods, the values of coefficient of variation were satisfactorily low and recovery was close to 100% [Table 2] for both the drugs. Hence it can be employed for routine analysis in quality control laboratories.
Table 2: Recovery Study Data of Tablet Formulation

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   Acknowledgements Top


The authors are thankful to Zydus Cadila for providing gift samples of pioglitazone and metformin.

 
   References Top

1.Reynolds JE. Martindale - The Extra Pharmacopoeia. 31st ed. London: The Royal Pharmaceutical Society; 1996. p. 81.  Back to cited text no. 1
    
2.Zarapkar SS, Halkar UP, Bhandari NP. Reverse phase high performance liquid chromatographic determination of ibuprofen, paracetamol and methocatbamol in tablets. Indian Drugs 1999;36:710-3.  Back to cited text no. 2
    
3.Davidson AG. Practical Pharmaceutical Chemistry. In: Beckett AH, Stenlake JB. editors. 4th ed. Vol. 2. New Delhi: CBS Publishers and Distributors; 2002. p. 284.  Back to cited text no. 3
    
4.Surmenian M. Simultaneous determination of ascorbic acid, pyridoxine hydrochloride, and tyrosine by derivative UV spectrophotometry. Drug Dev Ind Pharm 1998;24:691-6.  Back to cited text no. 4
    


    Figures

  [Figure 1], [Figure 2]
 
 
    Tables

  [Table 1], [Table 2]

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