Author(s): B. Mohammed Ishaq, K. Vanitha Prakash, G. Krishna Mohan

Email(s): prakash.karanam@gmail.com

DOI: Not Available

Address: B. Mohammed Ishaq1, Dr. K. Vanitha Prakash2*, Dr. G. Krishna Mohan3
1Research Scholar, Jawaharlal Nehru Technological University, Kakinada, A. P. India and Balaji College of Pharmacy, Anantapur, AP India 515001
2Department of Pharmaceutical Analysis, SSJ College of Pharmacy, Gandipet, Hyderabad (A.P.) India
3Centre for Pharmaceutical Sciences, IST, JNTU Hyderabad, Andhra Pradesh, India
*Corresponding Author

Published In:   Volume - 7,      Issue - 2,     Year - 2014


ABSTRACT:
A simple, rapid and sensitive isocratic RP-HPLC method was developed for the simultaneous estimation of Tapentadol and Paracetamol in bulk and their Pharmaceutical dosage form using Waters C18 (250 x 4.6 mm i.d, 5 micro particle size) analytical column in an isocratic mode with mobile phase comprising Acetonitrile: Potassium dihydrogen Phosphate pH 6.8 adjusted with orthophosphoric acid in the ratio of 50:50 (% v/v). The flow rate was 1.0 ml/ min and effluent was monitored at 215nm. The retention times were found to be 2.38 min for Paracetamol and 4.59 min for Tapentadol. The assay exhibited a linear dynamic range of 350-1050 microgram/ml for Paracetamol and 50-150 microgram/ml for Tapentadol. The calibration curve was linear (r = 1 for Paracetamol and r = 0.9998 for Tapentadol) over the entire linear range. Recovery was found to be 99.00 % + 0.41 for Paracetamol and 100 % + 0.22 for Tapentadol. The proposed method was statistically evaluated and validated as per ICH guidelines and can be applied for routine quality control analysis of Tapentadol and Paracetamol in Pharmaceutical dosage form.


Cite this article:
B. Mohammed Ishaq, K. Vanitha Prakash, G. Krishna Mohan. Development and Validation of RP-HPLC Method for Simultaneous Estimation of Tapentadol and Paracetamol in Bulk Drug and its Pharmaceutical Dosage Form. Research J. Pharm. and Tech. 7(2): Feb. 2014; Page 208-212.


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