It is the cache of ${baseHref}. It is a snapshot of the page. The current page could have changed in the meantime.
Tip: To quickly find your search term on this page, press Ctrl+F or ⌘-F (Mac) and use the find bar.

Simultaneous determination of clopidogrel and aspirin in pharmaceutical dosage forms Mishra P, Dolly A - Indian J Pharm Sci
Indian Journal of Pharmaceutical Sciences
Users online: 224
Scientific Publication of the Indian Pharmaceutical Association
Home Email this page Print this page Bookmark this page Decrease font size Default font size Increase font size
The Journal Search Current Issue Archives Instructions Online submission Login  


 
SHORT COMMUNICATION
Year : 2006  |  Volume : 68  |  Issue : 3  |  Page : 365-368
Simultaneous determination of clopidogrel and aspirin in pharmaceutical dosage forms


Department of Pharmaceutical Sciences, Dr. H. S. Gour University, Sagar-470 003, India,

Correspondence Address:
P Mishra
Department of Pharmaceutical Sciences, Dr. H. S. Gour University, Sagar-470 003, India

Login to access the Email id


DOI: 10.4103/0250-474X.26682

Get Permissions

   Abstract  

Two simple spectrophotometric methods for the determination of aspirin and clopidogrel in pharmaceutical formulations have been developed. First method is based on the additivity of absorbances. Second method is based on the determination of graphical absorbance ratio at two selected wavelengths, one being the isoabsorptive point for the two drugs (225 nm) and the other being the absorption maximum of hydrolysed aspirin (235.7 nm). Beer Lambert's law is obeyed for both the drugs in the concentration range 4-18 mg/ml. Both the methods were found to be simple, rapid, accurate and can be adopted in routine analysis of drugs in formulations. The accuracy and reproducibility of the proposed method was statistically validated by recovery studies.



How to cite this article:
Mishra P, Dolly A. Simultaneous determination of clopidogrel and aspirin in pharmaceutical dosage forms. Indian J Pharm Sci 2006;68:365-8

How to cite this URL:
Mishra P, Dolly A. Simultaneous determination of clopidogrel and aspirin in pharmaceutical dosage forms. Indian J Pharm Sci [serial online] 2006 [cited 2014 Mar 6];68:365-8. Available from: http://www.ijpsonline.com/text.asp?2006/68/3/365/26682


Acetylsalicylic acid (Aspirin) and clopidogrel hydrogen sulphate [S-(a)( 2- chlorophenyl)-6,7-dihydrothieno (3,2-C) pyridine-5 (4H) acetic acid methyl ester sulphate] are antiplatelet agents approved by the Food and Drug Administration, USA, for use in secondary prevention of heart attacks and stroke. Several spectrophotometric methods[1] and several HPLC methods[2],[3],[4],[5],[6],[7],[8],[9] have been reported for estimation of aspirin, whereas only HPLC methods are reported for estimation of clopidogrel in pharmaceutical dosage forms[10] and for its metabolite in plasma and serum[11]. Since clopidogrel and aspirin are marketed in combination and as no simultaneous methods are reported for the estimation of these drugs in combined dosage forms, we present two methods for their simultaneous estimation.

A GBC Cintra 10 UV/Vis spectrophotometer with 10 mm matched quartz cells was used for experiments. The chemicals used were of analytical grade. Sulphuric acid (Qualigens) (1 N) was prepared using distilled water. The commercially available tablets of clopidogrel and aspirin combination Deplatt A (Torrent, Ahmedabad) and Clopivas AP (Osaka, Satara, MH) and capsules Combiplet (Sun Pharma, Vadodara) were procured from local market. Clopidogrel (Dr. Reddy's Laboratories, Hyderabad) and Aspirin (Sischochem, Mumbai) were used as standard samples without further purification.

Stock solutions of clopidogrel and aspirin were prepared by dissolving 100 mg (accurately weighed) each of standard clopidogrel and standard aspirin separately in 100 ml of methanol. Working standard solutions (A) and (B) were further prepared by heating 1 ml of stock solutions of clopidogrel and aspirin respectively with 1 ml H 2 SO 4 for 30 min on water bath.

Method I is based on simultaneous equations method of Vierodt[12]. Aspirin shows two absorption maxima at 235.7 nm and 304.4 nm after acidic hydrolysis. Clopidogrel also absorbs at 235.7 nm but shows no absorption at 304.4 nm in the same condition. Calibration curve for clopidogrel and aspirin was prepared in the concentration range 4-18 mg/ml (range for which Beer Lambert's law followed) at 235.7 nm and for aspirin at 304.4 nm. The absorptivity coefficients were determined in this range and their average value taken. The overlain spectra of clopidogrel and aspirin are represented in [Figure - 1]. A set of two simultaneous equations was developed using these absorptivity coefficients. These are: A 1 =0.0170 Cy…(1); and A 2 =0.0196 Cx+0.0418 Cy…(2), where A 1 and A 2 are absorbances at 304.4 nm and 235.7 nm respectively, and Cx and Cy are concentrations of clopidogrel and aspirin respectively.

Method II is a graphical absorbance ratio method. This method is based on the method used by Ghanem et al.[13], which takes advantage of iso-absorptive point[14] of the two drugs, i.e., the wavelength of equal absorptivity of the two components of the mixture. The isoabsorptive point was found to be 225 nm in this case (l 1) [Figure - 1]. The other wavelength selected is the absorption maximum of one of the components. In this case, it was 235.7 nm, the absorption maximum of salicylic acid (l 2). The concentrations of the two components are related to the ratio of the absorbances at these two wavelengths. The absorbance of the mixture was noted at 235.7 nm and 225 nm. Calibration curves of aspirin and clopidogrel were plotted in the concentration range 4-18 mg/ml (range for which Beer Lambert's law was obeyed). The absorptivity coefficients were determined for both the drugs and the average value was taken. These values and the absorbance ratio were used to develop a set of two equations[14]. A 1 =0.0280 (Cx+Cy) (3); A 1 =0.0280 Cx [-0.79/(QM-1.49)] (4), where QM=A 2 /A 1, A 1 is absorbance at 225 nm and A 2 is absorbance at 235.7 nm. Cx and Cy are concentrations of clopidogrel and aspirin, respectively.

Twenty tablets of Clopivas AP were weighed and average weight was determined (before and after removing the coating). The tablets were finely powdered and powder equivalent to 100 mg of clopidogrel and 100 mg of aspirin was taken. In case of Deplatt A, powder equivalent to 100 mg of clopidogrel and 200 mg of aspirin was taken after determination of the average weight of tablet.

Average weight of twenty Combiplet capsules was determined and the capsule contents were emptied. Average weight of empty shells was again taken to determine the weight of the powder in each capsule. Powder obtained was mixed thoroughly; powder equivalent to 100 mg of clopidogrel and 100 mg of aspirin was taken.

In all the above three cases, the equivalent amount of powder taken was extracted with 4×20 ml of methanol and volume was made up to 100 ml to give the stock solutions. Working standard solutions were made in all the three cases by heating suitable dilutions of the stock with 1 ml H 2 SO 4 (1N). These were further suitably diluted and the absorbances were taken at different wavelengths as stated above .Using the equations 1, 2, 3, and 4, the concentrations were determined.

Both the methods were found to be accurate, simple, and rapid for routine simultaneous analysis of the formulations. In the first method, the content of the aspirin was directly found from the first equation at 304.4 nm, and substitution of this in second equation gives the concentration of clopidogrel. In the second method, the absorbance ratio and the absorptivity coefficients were determined, and the values were substituted in the equation given above to give the results. The reproducibility, repeatability, and accuracy of these methods were found to be good, which is evidenced by low values of standard deviation, percent relative standard deviation, and standard error [Table - 1]. The percent range of error (within 95% confidence limits) shows precision of the methods. To test the accuracy and reproducibility of the proposed methods, recovery experiments were performed by adding known amount of the drugs to the pre-analyzed formulations and reanalyzing the mixture by proposed methods[15]. Thus it can be concluded that the methods developed in the present investigation are simple, sensitive, accurate, and precise. Hence, these can be successfully applied for simultaneous estimation of clopidogrel and aspirin in pharmaceutical formulations.


   Acknowledgements   Top


The authors wish to thank Prof. N. K. Jain, Head of the Department, for providing necessary facilities; and Dr. Reddy's Laboratories Ltd., Hyderabad, for supplying clopidogrel as a gift sample. The financial assistance received from UGC in the form of fellowship for postgraduate studies in Engineering and Technology is being gratefully acknowledged by one of the authors (AD).

 
   References   Top

1. Sethi, P.D., Eds; In; Quantitative analysis of drugs in pharmaceutical formulations 3rd Edn, CBS publishers and distributors, New Delhi,1997,105.  Back to cited text no. 1    
2. Terweij-groen, C.P., Vahlkamp T.,and Kraak J.C., J. Chromatogr. , 1978,145,115  Back to cited text no. 2    
3. Cham, B.E., Ross-Lee, L., Bochner, F. and Imhoff, D.M., Clin. Chem. , 1979, 25, 1420.  Back to cited text no. 3    
4. Maulding, D.L. and Young, J.F., J. Pharm. Sci ., 1980,69,1224.  Back to cited text no. 4    
5. Berkersky, I., Boxenbaaum, H.G., Whitson, M.H., Puglisi, C.V., Pocelinko, R., and Kaplan, S.A., Anal. Lett ., 1977,10,539.  Back to cited text no. 5    
6. Harrison, L.I., Funk, M.L. and Ober, R.E., J. Pharm. Sci. , 1980,69,1268.  Back to cited text no. 6    
7. Lo, L.Y. and Bye, A., J. Chromatogr. , 1980,181,473.  Back to cited text no. 7    
8. Peng, G.W., Gadalla, M.A.F., Peng, A. and Chiou, W.L., J. Pharm. Sci . ,1978, 67,710.   Back to cited text no. 8    
9. Amick, E.N.and Mason,W.D., Anal. Lett. , 1979,12,629.  Back to cited text no. 9    
10. Mitakos, A. and Pander I. , J. Pharm. Biomed. Anal. , 2002, 431-438.  Back to cited text no. 10    
11. Lagorce, P., Perez, Y., Ortiz, J., Necciari, J. and Bressolle, F., J. Chromatogr. B. Biomed. Sci. Appl., 1998, 720(1:2),107-117.  Back to cited text no. 11    
12. Beckett, A.H. and Stenlake, J.B. In; Practical Pharmaceutical Chemistry, 4th Edn. Vol. II, CBS Publishers and Distributors, New Delhi, 1997, 278.  Back to cited text no. 12    
13. Ghanem, A., Meshali, M. and Foda, A., J. Pharm. Pharmacol., 1979, 31, 122.  Back to cited text no. 13    
14. Pernarowski, M., Knevel, A.M. and Christian, J.E., J. Pharm. Sci., 1960, 50, 943.  Back to cited text no. 14    
15. Reddy, N.R., Prabhavathi, K. and Chakravarthy, I.E., Indian J. Pharm. Sci., 2004, 66(2), 240-242.  Back to cited text no. 15    


    Figures

[Figure - 1]

    Tables

[Table - 1], [Table - 2]

This article has been cited by
1 STABILITY-INDICATING LC METHOD FOR THE ESTIMATION OF NIZATIDINE IMPURITIES IN NIZATIDINE ORAL SOLUTION
Papanaboina Venkata Rao,Maram Ravi Kumar,Vure Prasad,Dantu Durga Rao
Journal of Liquid Chromatography & Related Technologies. 2014; 37(7): 1065
[Pubmed]
2 Rapid and simultaneous determination of aspirin and dipyridamole in pharmaceutical formulations by reversed-phase high performance liquid chromatography (RP-HPLC) method
Prakash, K., Kalakuntla, R.R., Sama, J.R.
African Journal of Pharmacy and Pharmacology. 2011; 5(2): 244-251
[Pubmed]
3 Development of difference spectroscopic method for the estimation of Aspirin in formulation using hydrotropy
Bhattacharyya, I., Bhattacharyya, S.P., Talukdar, S., Medya, S.
International Journal of Research in Pharmaceutical Sciences. 2011; 2(1): 84-87
[Pubmed]
4 A validated stability-indicating normal phase LC method for clopidogrel bisulfate and its impurities in bulk drug and pharmaceutical dosage form
Dantu Durga Rao,L. Kalyanaraman,Shakil S. Sait,P. Venkata Rao
Journal of Pharmaceutical and Biomedical Analysis. 2010; 52(1): 160
[Pubmed]
5 Ion-pairing RP-HPLC method for simultaneous determination of aspirin and clopidogrel bisulphate in tablet and capsule dosage form
Panda, S.S.
International Journal of PharmTech Research. 2010; 2(1): 269-273
[Pubmed]
6 Simultaneous determination of paracetamol, acetyl salicylic acid, mefenamic acid and cetirizine dihydrochloride in the pharmaceutical dosage form
Havaldar, F.H., Vairal, D.L.
E-Journal of Chemistry. 2010; 7(sup 1): 495-503
[Pubmed]
7 Spectrophotometric simultaneous determination of aspirin and Ticlopidine in combined tablet dosage form by first order derivative spectroscopy, Area Under Curve (AUC) and ratio derivative spectrophotometric methods
Gujarathi, S.C., Shah, A.R., Jagdale, S.C., Datar, P.A., Choudhari, V.P., Kuchekar, B.S.
International Journal of Pharmaceutical Sciences Review and Research. 2010; 3(1): 115-119
[Pubmed]
8 A validated stability-indicating normal phase LC method for clopidogrel bisulfate and its impurities in bulk drug and pharmaceutical dosage form
Durga Rao, D., Kalyanaraman, L., Sait, S.S., Venkata Rao, P.
Journal of Pharmaceutical and Biomedical Analysis. 2010; 52(1): 160-165
[Pubmed]
9 Electrochemical study of the antiplatelet agent clopidogrel and its determination using differential pulse voltammetry in bulk form and pharmaceutical preparations with a glassy carbon electrode
Dermiş, S., Aydoǧan, E.
Pharmazie. 2010; 65(3): 175-181
[Pubmed]
10 Separation and determination of clopidogrel and its impurities by capillary electrophoresis
Fayed, A.S., Weshahy, S.A., Shehata, M.A., Hassan, N.Y., Pauwels, J., Hoogmartens, J., Van Schepdael, A.
Journal of Pharmaceutical and Biomedical Analysis. 2009; 49(2): 193-200
[Pubmed]
11 Validated column high-performance liquid chromatographic method for determination of aspirin and clopidogrel in combined tablets in the presence of degradation products formed under ICH-recommended stress conditions
Kachhadia, P.K., Doshi, A.S., Joshi, H.S.
Journal of AOAC International. 2009; 92(1): 152-157
[Pubmed]
12 Separation and determination of clopidogrel and its impurities by capillary electrophoresis
Ahmed S. Fayed,Soheir A. Weshahy,Mostafa A. Shehata,Nagiba Y. Hassan,Jochen Pauwels,Jos Hoogmartens,Ann Van Schepdael
Journal of Pharmaceutical and Biomedical Analysis. 2009; 49(2): 193
[Pubmed]



 

Top
Print this article  Email this article
 
  Search
   
   Next article
   Previous article 
   Table of Contents
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Article in PDF (151 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
    Acknowledgements
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed 8278    
    Printed 112    
    Emailed 10    
    PDF Downloaded 517    
    Comments  [Add]    
    Cited by others  12    

Recommend this journal