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
Link To Document :
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