All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Abstract

Validated TLC densitometric method for the quantification of paroxetine hydrochloride in solid dosage form

Author(s): RN Sharma1, MS Bagul2, SC Chaturvedi1, KK Vasu2, M Rajani2
1 School of Pharmacy, Devi Ahilya Vishwavidyalaya, Indore - 452 017, India 2 B. V. Patel Pharmaceutical Education and Research Development (PERD) Centre, Thaltej-Gandhinagar Highway, Thaltej, Ahmedabad - 380 054, India

Correspondence Address:
M Rajani B. V. Patel Pharmaceutical Education and Research Development (PERD) Centre, Thaltej-Gandhinagar Highway, Thaltej, Ahmedabad - 380 054 India E-mail: perd@perdcentre.com


A simple, specific, accurate and precise high performance thin layer chromatography method has been developed for the estimation of paroxetine hydrochloride in tablet dosage forms. The quantification was carried out at 296 nm. Developed method was validated in terms of linearity, accuracy, precision, repeatability and specificity. Limit of detection and limit of quantification of paroxetine hydrochloride were found to be 60 ng/spot and 160 ng/spot, respectively. The linearity range for paroxetine hydrochloride was found to be 160-960 ng/spot with correlation coefficient of 0.995. Content of paroxetine hydrochloride in two tablet dosage forms was found to be 100.10 and 100.20%, respectively.

Full-Text | PDF

 
 
Google scholar citation report
Citations : 66710

Indian Journal of Pharmaceutical Sciences received 66710 citations as per google scholar report