Title of article
Reversed Phase High Performance Liquid Chromatographic Method for Simultaneous Estimation of Eperisone Hydrochloride and Paracetamol in Tablet Dosage Form
Author/Authors
بابان محيط، پوپات نويسنده Department of Pharmaceutical Chemistry and PG Studies, M.E.S. College of Pharmacy, Sonai, Tq?Newasa, Dist.?Ahmednagar, Maharashtra, India?414105. Baban Mohite, Popat , گاجانان خناگ، شانتارام نويسنده Department of Pharmaceutical Chemistry and PG Studies, M.E.S. College of Pharmacy, Sonai, Tq?Newasa, Dist.?Ahmednagar, Maharashtra, India?414105. Gajanan Khanage, Shantaram , شانكار جاداو، سانديپ نويسنده Department of Pharmaceutical Chemistry and PG Studies, M.E.S. College of Pharmacy, Sonai, Tq?Newasa, Dist.?Ahmednagar, Maharashtra, India?414105. Shankar Jadhav, Sandip
Issue Information
دوفصلنامه با شماره پیاپی 0 سال 2015
Pages
6
From page
57
To page
62
Abstract
در اين كار يك روش دقيق، ساده و گزينش پذير بنام كروماتوگرافي مايع با كارآيي بالا با فاز برگشتي براي اندازه گيري دو تركيب دارويي اپريسون هيدروكلريد و پاراستامول توسعه يافت. رنج خطي براي اين دو تركيب عبارت بود از 25-5 ميكروگرم بر ميلي ليتر و بازيافت ها براي هر دو تركيب در گستره اي بين 87/99 تا 52/100 درصد بدست آمد كه نشان دهنده صحت روش حاضر در تعيين هم زمان آن در نمونه هاي دارويي به كاررفته مي باشد
Abstract
Eperisone Hydrochloride is a skeletal muscle relaxant and Paracetamol is cyclooxygenase inhibitor. These drugs in combination are used as antispasmodics. A simple, specific, precise and accurate method was developed, namely reverse phase high performance liquid chromatography for simultaneous estimation of Eperisone Hydrochloride and Paracetamol in tablet dosage form. In RP-HPLC method separation was achieved by HiQ silC-18HS column having 250 mm× 4.6 mm, with mobile phase containing Methanol: 0.05 mM Ammonium acetate buffer: Acetonitrile (60:30:10) and adjusted to pH 5.8 using Glacial acetic acid for RP-HPLC system. The flow rate was 1.0 ml/min and effluent was monitored at 264 nm. The retention time of EPR and PAR were 6.45 min and 3.05 min respectively. The linearity for EPR and PAR were in the range of 5-25 µg/mL. The recoveries of EPR and PAR were found in the range of 99.96-100.52% and 99.87-100.11%, respectively. The proposed method was validated as per ICH guidelines and successfully applied to the estimation of EPR and PAR in tablet dosage form.
Journal title
Iranian Journal of Analytical Chemistry
Serial Year
2015
Journal title
Iranian Journal of Analytical Chemistry
Record number
2395761
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