SIMULTANEOUS SPECTROPHOTOMETRIC ESTI-MATION OF CAMYLOFIN DIHYDROCHLORIDE AND DICLOFENAC POTASSIUM IN TABLET DOS-AGE FORM
Keywords:
Camylofin Dihydrochloride, Diclofenac Potassium, Validation, Simultaneous equation methodAbstract
The accurate, precise, sensitive and economical spectrophotometric method was developed and validated for simultaneous estimation of Camylofin Dihydrochloride and Diclofenac Potassium tablet dosage form. The method employed for UV estimation was simultaneous equation method. The method employs 248 nm as ?1 and 280 nm as ?2 for formation of equations. Camylofin Dihydrochloride and Diclofenac Potassium obeys Beer’s law in the concentration range 5-80 ?g/mL (r2=0.998) and 5-80 ?g/mL (r2=0.997). The mean recovery for Camylofin Dihydrochloride and Diclofenac Potassium, were found to be 99.652 ±0.2129% and 99.80 ±0.0.00307% respectively. The developed method were validated according to ICH guidelines and values of accuracy, precision and other statistical analysis were found to be in good accordance with the prescribed values. Thus the proposed methods were successfully applied for simultaneous determination of Camylofin Dihydrochloride and Diclofenac Potassium, routine analytical work.
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References
Christian G.D., Analytical Chemistry, 4th Edn, John Wiley and sons, United Kingdom, 1986, P. 1-6.
Kennedy J.H., Analytical Chemistry-Principals, 2nd Edn, Saunders College Publishing, New York, 1990, P. 1-8.
Sharma B.K. (Eds.), Instrumental Methods of Chemical Analysis, 11th Edn, Goel Publishing House, Meerut, 1991, P. 1-9.
http://www.medgyan.com/indexpop.php?option=drug-effects&drId=53203
https://en.wikipedia.org/wiki/Camylofin
https://pubchem.ncbi.nlm.nih.gov/compound/Diclofenac_potassium#section=Names-and-Identifiers
http://www.drugbank.ca/drugs/DB00586
Kadam N.N., Patil.P.C., Singh.R.R., A stability indicating Rphplc determination of camylofin dihydrochloride in drug substance., 2011 Int J Pharm Pharm Sci, vol 3, issue 3, , 153-158
Rathnam M.V., Singh R.R. Simultaneous RP HPLC Determination of Camylofin Dihydrochloride and Diclofenac Potassium in Pharmaceutical Preparations., Pharm Anal Acta, 1:108.
Singh R.R., Rathnam M.V., Singh S.J., and Vegesna R.V.K., Stability Indicating Method for Simultaneous RP HPLC Determination of Camylofin Dihydrochloride and Nimesulide in Pharmaceutical Preparations., ISRN Analytical Chemistry., Volume 2012, 7.
Singh R.R., Rathnam M.V., Singh S.J., and Vegesna R.V.K., A stability indicating GC-FID method for camylofin dihydrochloride and diclofenac potassium in pharmaceutical preparation., Int J Pharm Pharm Sci, Vol 4, Issue 1, 317-324.
Singh R.R., Rathnam M.V., Singh S.J., and Vegesna R.V.K., “Determination of Camylofin Dihydrochloride and Nimesulide in Pharmaceutical preparation by Gas Chromatography”, American Journal of Analytical Chemistry, 2, 2011, 944-952.
Patel H., Kotadiya B., Patel P., Development and validation of uv spectroscopic methods for simultaneous estimation of camylofin dihydrochloride and paracetamol in combined dosage form., 2014, inventi:ppaqa,1402,14.
Jadhav S.D., Butl S.R., Patil S.D., Jagtap P.K., Validated stability indicating RP-HPLC method for simultaneous determination and in vitro dissolution studies of thiocolchicoside and diclofenac potassium from tablet dosage form., Arabian Journal of Chemistry (2015) 8, 118–128.
Degwy M.A., Aly M.A.M. and Den M.S.El., Development And Validation of A Hplc Method for In-Vivo Study Of Diclofenac Potassium., Degwy et al., IJPSR, 2013; Vol. 4(2): 622-627.
Divya Bharathi K., Begum S., Vaddepally L., and Tulja R.G., Development And Validation of New Rp-Hplc Method for Simultaneous Estimation of Metaxalone and Diclofenac Potassium in Tablet Dosage Form., International Journal Of Research In Pharmacy And Chemistry, 2015, 5(1), 222-229.
Naveed S., Rehman H., Qamar F., Zainab S., Development of a spectrophotometric method for the assay of Diclofenac potassium.; Journal of Innovations in Pharmaceuticals and Biological Sciences, 2015; Vol 2 (1), 7-11.
Vinod K.K., Sudhakar M., Reddy P.Y., Ravindra A., Validated RP- HPLC Method for Simultaneous Esti-mation of Metax alone and Diclofenac potassium in Combined Dosage Form Am. J. PharmTech Res. 2013; 3(4) 750-758.
Gowramma B.S., Muralidharan R.S., Meyyanathan S.N and Suresh B., A validated Rp-hplc method for simultaneous estimation of paracetamol and diclofenac potassium in pharmaceutical formulation., International Journal of ChemTech Research Res.2010,Vol 2(1) 676-680.
Vijjigiri C., Daravath B., Kamarapu S.K., Method Development And Validation Of Rp-Hplc Method For Simultaneous Estimation Of Dicyclomine Hydrochloride And Diclofenac Potassium In Tablet Dosage Forms., International Journal of Pharmacy and Biological Sciences, 2013 Volume 3, Issue 4, 255-264.
Sindhur N.N., Gouthami B., Madhuri L., Krishnaveni N., Meyyanathan S.N and Suresh B., Development and validation of a RP-HPLC method for the simultaneous determination of paracetamol and diclofenac potassium on stainless steel surface of pharmaceutical manufacturing equipments., Journal of Chemical and Pharmaceutical Research, 2012, 4(3):1670-1675.
Wadi N.M., Khalid S., Khiang P.K and Ahuja A., Development and Evaluation a Simultaneous Assay Method of Metronidazole and Diclofenac Potassium in A Pharmaceutical Formulation., Vol. 7, No. 2, 2333-2339.
Pand S.S., Patanaik D., Ravi Kumar B.V.V., New Stability-Indicating RP-HPLC Method for Determination of Diclofenac Potassium and Metaxalone from their Combined Dosage Form., Sci Pharm. 2012; 80: 127–137.
Patel C.R., Kimbahune R.V., Kabra P.V., Harish A.R and Nargund L.V.G., Spectrophotometric Estimation of Metaxalone and Diclofenac Potassium by Multicomponent Analytical Method from Tablet Dosage Form., J Anal Bioanal Techniques 2012, 3:3, 1-3.
ICH, Draft Guideline on Validation of Analytical Procedures, Definition and Terminology, Federal Register, 1995, 60 FR 11260.
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