alexa Determination of Carteolol in Pure and Pharmaceutical F
ISSN: 2161-0444

Medicinal chemistry
Open Access

Like us on:
OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations

700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Research Article

Determination of Carteolol in Pure and Pharmaceutical Formulation by Spectrophotometric Method

Malek Okdeh*, Chahid Moustpha and Mohammad Shraitah

Department of Chemistry, Faculty of Science, Teshreen University, Lattakia, Syria

*Corresponding Author:
Malek Okdeh
Department of Chemistry, Faculty of Science
Teshreen University
Lattakia, Syria
Tel: 96341352451
E-mail: [email protected]

Received date: January 18, 2016; Accepted date: February 11, 2016; Published date: February 15, 2016

Citation: Okdeh M, Moustpha C, Shraitah M (2016) Determination of Carteolol in Pure and Pharmaceutical Formulation by Spectrophotometric Method. Med chem (Los Angeles) 6:115-118. doi:10.4172/2161-0444.1000334

Copyright: © 2016 Okdeh M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

An accurate, simple, fast, and good sensitive Spectrophotometric method have been developed for the determination of Carteolol based on the formation of complex (ion-pair complexes) between the Carteolol (CRT) and Alizarin yellow R Sodium salt (AR) at pH=11.20. This reaction produces a complex red color which is absorbed maximally at 500 nm. Beer’s law was obeyed in the range of 1.80-197.30 ug/mL with molar absorptivity of 1.7663×103 L mole-1cm-1. The effects of analytical parameters on the reported system were investigated. The results were validated statistically. The proposed method was applied to commercially available tablets. Interferences of the other ingredients and excipients were not observed.

Keywords

Share This Page

Additional Info

Loading
Loading Please wait..
 
Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
adwords