<?xml version="1.0" encoding="UTF-8"?>
<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>World Journal of Analytical Chemistry</journalTitle>
<publicationDate>2013-04-19</publicationDate>
<volume>1</volume>
<issue>1</issue>
<startPage>18</startPage>
<endPage>22</endPage>
<doi>10.12691/wjac-1-2-1</doi>
<publisherRecordId>WJAC2013121</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Development and Validation of Spectrophotometric Method for Determination of Penicillamine (PA) in Pharmaceutical Formulation Using 4-Choro-Nitrobenzo-2-Oxa-1, 3-Diazol (NBD-CL)</title>
<authors>
<author>
<name>Abdalla Ahmed Elbashir</name>
<email>hajaae@yahoo.com</email>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Amira Anwar Babikir Alfadil</name>
<affiliationId>2</affiliationId>
</author>

</authors>
<affiliationsList>
<affiliationName affiliationId="1">University of Khartoum, Faculty of Science, Chemistry Department, Khartoum, Sudan</affiliationName>
<affiliationName affiliationId="2">University of Sudan for Science & Technology, Faculty of Science, Department of chemical Laboratory, Khartoum, Sudan</affiliationName>
</affiliationsList>
<abstract language="eng">A sensitive and simple spectrophotometric method has been proposed for the determination of D-Penicillamine (PA) in pharmaceutical formulations. The proposed method is based on the reaction between the PA and 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole (NBD-CL) at alkaline medium (pH 10.5) to form deep brown-purple adduct, exhibiting maximum absorption (¦Ë<SUB>max</SUB>) at 468nm. Under optimized reaction condition, the method was linear in the concentration range 1-15¦Ìg mL<SUP>-1</SUP>. The limit of detection (LOD) and limit of quantification (LOQ) were found to be 0.11¦Ìg mL<SUP>-1</SUP>, 0.38¦Ìg mL<SUP>-1</SUP>, respectively. The method was applied successfully to the determination of PA in pharmaceutical dosage form. A proposal of the reaction pathway has been postulated. The results were in a good agreement with those obtained with the official USP method. The method is useful for routine analysis of PA in quality control laboratories.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/wjac/1/2/1/wjac-1-2-1.pdf</fullTextUrl>
<keywords language="eng"><keyword>D-Penicillamine</keyword>
<keyword>spectrophotometric</keyword>
<keyword>pharmaceutical formulation</keyword>
<keyword>method validation</keyword>
<keyword>NBD-CL</keyword>
</keywords>
</record>
</records>
