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    	<title>IJPRS/V2/I1/00003 - 08/01/2013</title>

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		<title>Development of Reverse Phase  Liquid Chromatographic Method for Determination of (+)-(S)-(o-Chlorophenyl)-6,7-Dihydrothieno [3,2-c] pyridine-5(4H)-acetic acid,Hydrochloride and Methyl (+/-)  &#8211; (o-Chloro phenyl)-4,5-Dihydrothieno[2,3-c]pyridine-6(7H)-acetate, Hydrochloride  from Clopidogrel Besylate</title>
		
		<description><![CDATA[<h5>Author's Affiliation</h5>
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                                                    	<h5>Abstract</h5>
		                                                <p>Clopidogrel besylate contain single stereogenic center and has impurities like ((+) - (S) - (o-chlorophenyl)-6,7-dihydrothieno[3,2-c] pyridine-5(4H)- acetic acid, hydrochloride) which is known as impurity A and (Methyl (+/-) - (o-chloro phenyl)-4,5-dihydrothieno[2,3-c] pyridine-6(7H)-acetate, hydrochloride) which is known as impurity B. They are introduced during production. A simple, sensitive, precise and high performance liquid chromatographic (HPLC) method has been developed and validated for quantitative determination of impurity A and impurity B from clopidogrel besylate in bulk drug using uv detector at 220 nm. The developed method was able to separate impurity A and impurity B of clopidogrel besylate from its bulk drug within 50 min. The chromatographic separation was carried out by reverse phase chromatography using C<sub>8</sub> column (Zorbax SB C<sub>8</sub> 250 mm x 4.6 mm x 5 µm), with mobile phase comprising of buffer solution and acetonitrile in the gradient composition, at a flow rate of 1.0 ml/min, at 25°C temperature. The limit of detection  and limit of quantitation  of impurity A were found to be 0.07 µg/ml and 0.20 µg/ml and of impurity B were found to be 0.10 µg/ml and 0.30 µg/ml respectively. The linearity of response of impurity A was in the range of 0.20 µg/ml to 3.0 µg/ml with r &gt; 0.9999. The linearity of response of impurity B was in the range of 0.30 µg/ml to 4.5 µg/ml with r &gt; 0.9995. The method was validated and found to be suitable for determination of impurity A and impurity B from clopidogrel besylate bulk drug.</p>
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                                                        <h5>Keywords</h5>
                                                         <p>Clopidogrel besylate, ((+)-(S)-(o-chlorophenyl)-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-acetic acid,          hydrochloride)   i.e. (impurity A), (Methyl (+/-) - (o-chloro phenyl)-4,5-dihydrothieno[2,3-c]pyridine-6(7H)-acetate, hydrochloride) i.e. (impurity B), High performance liquid chromatography, Method validation and quantitation.Nephrotoxicity, Anti-tubercular drugs, Thymoquinone</p>
                                                         
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                                                         <h5>Cite This Article</h5>
                                                         <p>Pawaskar, P. S., Dighe, V. V., Adhyapak, S. S., Shambhu, N. S., &amp; Mestry, D. Y. (2013). Development of Reverse Phase Liquid Chromatographic Method for Determination of (+)-(S)-(o-Chlorophenyl)-6,7-Dihydrothieno [3,2-c] pyridine-5(4H)-acetic acid,Hydrochloride and Methyl (+/-) - (o-Chloro phenyl)-4,5-Dihydrothieno[2,3-c]pyridine-6(7H)-acetate, Hydrochloride from Clopidogrel Besylate. <em>International Journal for Pharmaceutical Research Scholars (IJPRS), 2(1),</em> 16-23.</p>                                                         <hr/>
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		<link>https://www.ijprs.com/article/development-of-reverse-phase-liquid-chromatographic-method-for-determination-of-s-o-chlorophenyl-67-dihydrothieno-32-c-pyridine-54h-acetic-acidhydrochloride-and-methyl-o-chlo/</link>
		<author>Pawaskar, P. S., Dighe, V. V., Adhyapak, S. S., Shambhu, N. S., Mestry, D. Y.        </author>

		<pdflink>http://www.ijprs.com/wp-content/uploads/2018/09/IJPRS-V2-I1-00003.pdf</pdflink>

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