Indian Journal of Pharmaceutical Sciences
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Year : 2006  |  Volume : 68  |  Issue : 5  |  Page : 639-640
UV spectrophotometric simultaneous estimation of valdecoxib and paracetamol in combined tablet dosage form


J. L. Chaturvedi College of Pharmacy, New Nandanvan, Nagpur-440 009, India

Date of Submission06-May-2005
Date of Decision31-Oct-2005
Date of Acceptance01-Oct-2006

Correspondence Address:
Vaishali Nagulwar
J. L. Chaturvedi College of Pharmacy, New Nandanvan, Nagpur-440 009
India
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DOI: 10.4103/0250-474X.29634

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   Abstract 

The present work deals with the development of a simple, accurate and economical method for the simultaneous estimation of valdecoxib and paracetamol in combined tablet dosage form by Vierodt's UV spectrophotometric method. The λmax values of valdecoxib and paracetamol in 0.1 N NaOH were 244 nm and 257 nm respectively. Both the drugs followed Beer's law in the concentration range of 1-6 g/ml and 5-30 g/ml respectively. The A1% 1 cm values for valdecoxib and paracetamol at 244 nm and 257 nm were 520 and 420, 510.8 and 636.8 respectively.



How to cite this article:
Nagulwar V, Dhurvey Y R, Deshpande S, Upadhye K, Bakhle S, Wadetwar R. UV spectrophotometric simultaneous estimation of valdecoxib and paracetamol in combined tablet dosage form. Indian J Pharm Sci 2006;68:639-40

How to cite this URL:
Nagulwar V, Dhurvey Y R, Deshpande S, Upadhye K, Bakhle S, Wadetwar R. UV spectrophotometric simultaneous estimation of valdecoxib and paracetamol in combined tablet dosage form. Indian J Pharm Sci [serial online] 2006 [cited 2014 Sep 2];68:639-40. Available from: http://www.ijpsonline.com/text.asp?2006/68/5/639/29634


Valdecoxib, chemically 4, 5, (5-methyl-3-phenylisoxazol-4-yl) benzene sulphonamide, is a new COX-2 inhibitor and an antiinflammatory drug[1],[2]. It is yet not official in any pharmacopoeia. Paracetamol is an antipyretic and analgesic, official in Indian Pharmacopoeia[3] and in Martindale[4]. Chemically, it is N-(4-hydroxyphenyl) acetamide. Both the drugs in combination are used for the synergistic activity. Literature survey revealed various methods for the determination of paracetamol in combination with other drugs[5],[6],[7],[8],[9], but no method was found to be developed for its estimation with valdecoxib in combined dosage forms. The authors have hence developed Vierodt's method[10] for the simultaneous estimation of valdecoxib and paracetamol in pharmaceutical solid dosage form.

Pure drug paracetamol was obtained from Universal Medicaments Pvt. Ltd., Shanti Nagar, Nagpur, and valdecoxib was provided by Mepro Pharmaceuticals Pvt. Ltd., Surendranagar, Gujarat. Shimadzu 1601 spectrophotometer with 10 mm matched quartz cells was used for the spectral observations. Sodium hydroxide (analytical grade) and double-distilled water were used for the present study.

Stock solutions (1 mg/ml) of both the drugs were prepared in 0.1 N NaOH. For the verification of Beer's law, a series of diluted solutions of valdecoxib and paracetamol ranging from 1-6 g/ml and 5-30 g/ml respectively, and mixture of both the drugs were prepared in 0.1 N NaOH. It was observed that valdecoxib and paracetamol individually, as well as in their mixtures, gave a good linearity response.

For the estimation of pure drugs by the proposed method, solutions of 1 g/ml valdecoxib and 25 g/ml of paracetamol and a mixture containing 1 g/ml and 25 g/ml of both the drugs were selected for determination of absorbance values. The contents were calculated using the following equations. C x =(A 2 ay 1 -A 1 ay 2 )/(ax 2 ay 1 -ax 1 ay 2 ), C Y =(A 1 ax 2 -A 2 ax 1 )/(ax 2 ay 1 -ax 1 ay 2 ), where C x and Cy are the concentrations of valdecoxib and paracetamol respectively, ax 1 and ax 2 are the absorptivity values of valdecoxib at 244 nm and at 257 nm respectively, ay 1 and ay 2 are the absorptivity values of paracetamol at 244 nm and at 257 nm respectively and A 1 and A 2 are the absorbances of the diluted sample at 244 nm and at 257 nm respectively.

For the estimation of drugs in the marketed preparations, 20 tablets containing 20 mg valdecoxib and 500 mg paracetamol (Valeron Plus and Coxval-P) were weighed and finely powdered. A quantity of powder equivalent to 10 mg valdecoxib and 250 mg paracetamol was accurately weighed and transferred to a 50 ml volumetric flask, dissolved in 0.1 N NaOH, and the solution was filtered through Whatman filter paper no. 1 and the volume was made up to the mark with the same solvent. Aliquots of this tablet solution were diluted to get the concentrations ~ 1 g/ml of valdecoxib and ~ 25 g/ml of paracetamol. The sample solutions were scanned over the range of 190-400 nm. Absorbance of the sample solutions at 244 nm and 257 nm was measured and from the absorbance values, the concentration of drugs in the sample solution was determined by using Vierodt's formula. The amount and % claim calculated for both the drugs are shown in [Table - 1].

To study the accuracy and precision of the proposed method, recovery studies were carried out by adding a known quantity of standard to the preanalyzed sample. The procedure was repeated five times, and it was observed that the excipients present in the tablets did not interfere in the estimation of valdecoxib and paracetamol. The percent recovery calculated is shown in [Table - 2]. The optical characteristics such as Beer's law limits, detection limit, molar absorptivities and Sandell's sensitivities are presented in [Table - 2].

Thus the proposed method is simple, accurate, precise and economical for routine analysis of two drugs without prior separation. The amount found was in good agreement with the labelled claim of the formulation. The value of standard deviation was satisfactorily low, indicating the reproducibility and accuracy of the method developed.


   Acknowledgements Top


The authors are thankful to Mepro Pharmaceutical Pvt. Ltd., Gujarat; and Universal Medicaments Pvt. Ltd., Nagpur, for providing the pure drugs. They are also grateful to Dr. V. D. Rangari, Principal, J. L. Chaturvedi College of Pharmacy, Nagpur, for his kind cooperation in the completion of this work.

 
   References Top

1.Shastry, C.S., Joshi, S.D., Veerapur, V.P. and Arvind, M.B., Indian J. Pharm. Edu. , 2003, 37, 154.   Back to cited text no. 1    
2.Sutariya, V.B., Mashru, R., Sankalia, M.G. and Parikh, P., Indian J. Pharm. Sci. 2004, 66, 360.  Back to cited text no. 2    
3.Indian Pharmacopoiea , 4th Edn., Vol. II, Controller of Publications, Delhi, 1996, 554.  Back to cited text no. 3    
4.Reynolds, J.E.F., In: Martindale. The Extra Pharmacopoeia , 31st Edn., The Royal Pharmaceutical Society, London, 1996, 81.  Back to cited text no. 4    
5.Vasudevan, M., Ravishankar, S., Ravibabu, T. and Nagarajan, J.S.K., Indian J. Pharm. Sci., 2000, 62, 122.  Back to cited text no. 5    
6.Dhake, A.S., Sonaje, D.B., Kasture, V.S., Nikam, P.T. and Talekar, R. S., Indian J. Pharm. Sci., 2001, 63, 55.  Back to cited text no. 6    
7.Zarapkar, S.S., Halkar, U.P. and Bhandari, N.P., Indian Drugs , 1999, 36, 710.  Back to cited text no. 7    
8.Gangwal, S. and Trivedi, P., Indian Drugs , 1999, 36, 683.  Back to cited text no. 8    
9.Kumar, A., Anroop, B. and Vijay, K.S., Indian Drugs , 2003, 40, 727.  Back to cited text no. 9    
10.Davidson, A.G., In: Beckett, A.H. and Stenlake, J.B., Eds., Practical Pharmaceutical Chemistry, 4th Edn., Vol.II, CBS publishers and Distributors, New Delhi, 2002, 284.  Back to cited text no. 10    


    Tables

[Table - 1], [Table - 2]

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