Next Article in Journal
Development of a Stability-Indicating RP-UPLC Method for Rapid Determination of Metaxalone and its Degradation Products in Solid Oral Dosage Form
Previous Article in Journal
Liposomes for Topical Use: A Physico-Chemical Comparison of Vesicles Prepared from Egg or Soy Lecithin
 
 
Scientia Pharmaceutica is published by MDPI from Volume 84 Issue 3 (2016). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Austrian Pharmaceutical Society (Österreichische Pharmazeutische Gesellschaft, ÖPhG).
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Application of HPLC for the Simultaneous Determination of Aceclofenac, Paracetamol and Tramadol Hydrochloride in Pharmaceutical Dosage Form

by
Preeti CHANDRA
,
Atul Singh RATHORE
,
Sathiyanarayanan LOHIDASAN
and
Kakasaheb Ramoo MAHADIK
*
Department of Pharmaceutical Chemistry, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Erandwane, Pune-411038, Maharashtra, India
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2012, 80(2), 337-352; https://doi.org/10.3797/scipharm.1108-04
Submission received: 5 August 2011 / Accepted: 31 January 2012 / Published: 31 January 2012

Abstract

A simple, precise and accurate reversed-phase liquid chromatographic method has been developed for the simultaneous estimation of aceclofenac (ACF), paracetamol (PCM) and tramadol hydrochloride (TRM) in pharmaceutical dosage form. The chromatographic separation was achieved on a HiQ-Sil™ HS C18 column (250×4.6 mm i.d., 5 μm particle size), kromatek analytical column at ambient temperature. The mobile phase consisted of 40: 60 (v/v); phosphate buffer (pH 6.0): methanol. The flow rate was set to 1.0 mL min−1 and UV detection was carried out at 270 nm. The retention time (tR) for ACF, PCM and TRM were found to be 14.567 ± 0.02, 3.133 ± 0.01 and 7.858 ± 0.02 min, respectively. The validation of the proposed method was carried out for linearity, precision, robustness, limit of detection, limit of quantitation, specificity, accuracy and system suitability. The linear dynamic ranges were from 40–160 μg mL−1 for ACF, 130–520 μg mL−1 for PCM and 15–60 μg mL−1 for TRM. The developed method can be used for routine quality control analysis of titled drugs in pharmaceutical dosage form.
Keywords: Aceclofenac; Paracetamol; Tramadol hydrochloride; Method development; Validation; HPLC Aceclofenac; Paracetamol; Tramadol hydrochloride; Method development; Validation; HPLC

Share and Cite

MDPI and ACS Style

CHANDRA, P.; RATHORE, A.S.; LOHIDASAN, S.; MAHADIK, K.R. Application of HPLC for the Simultaneous Determination of Aceclofenac, Paracetamol and Tramadol Hydrochloride in Pharmaceutical Dosage Form. Sci. Pharm. 2012, 80, 337-352. https://doi.org/10.3797/scipharm.1108-04

AMA Style

CHANDRA P, RATHORE AS, LOHIDASAN S, MAHADIK KR. Application of HPLC for the Simultaneous Determination of Aceclofenac, Paracetamol and Tramadol Hydrochloride in Pharmaceutical Dosage Form. Scientia Pharmaceutica. 2012; 80(2):337-352. https://doi.org/10.3797/scipharm.1108-04

Chicago/Turabian Style

CHANDRA, Preeti, Atul Singh RATHORE, Sathiyanarayanan LOHIDASAN, and Kakasaheb Ramoo MAHADIK. 2012. "Application of HPLC for the Simultaneous Determination of Aceclofenac, Paracetamol and Tramadol Hydrochloride in Pharmaceutical Dosage Form" Scientia Pharmaceutica 80, no. 2: 337-352. https://doi.org/10.3797/scipharm.1108-04

Article Metrics

Back to TopTop