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<journal-id journal-id-type="publisher">london-journal-of-medical-and-health-research</journal-id>
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<journal-title>London Journal of Medical and Health Research</journal-title>
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<issn publication-format="print">2515-5784</issn>
<issn publication-format="electronic">2515-5792</issn>
<publisher><publisher-name>JournalsPress</publisher-name></publisher>
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<article-id pub-id-type="publisher-id">89240</article-id>
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<article-title>Development and Validation of Uv Spectrophotometric Estimation of Perindopril Erbumine and Indapamide in Bulk and Tablet Dosage by Using Area Under Curve Method</article-title>
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<volume>23</volume>
<issue>1</issue>
<fpage>33</fpage>
<lpage>39</lpage>
<abstract><p>A simple, precise, accurate, and economical UV visible spectrophotometric method has been developed for estimation of Perindopril erbumine &amp; Indapamide drug by AUC method. Quantitative determination of the drug was performed at wavelength range 208-214 nm and 239-244 nm for Perindopril erbumine &amp; Indapamide respectively. The linearity was established over the concentration range of 10-50 µg/ml for Perindopril erbumine and 1-5 µg/ml for Indapamide with correlation coefficient value of 0.999 for both the drugs. Precision studies showed that % relative standard deviation was within range of acceptable limits. The recovery study was found to be within range of 99-101%. The proposed method has been validated as per ICH guidelines.</p></abstract>
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<p>A simple, precise, accurate, and economical UV visible spectrophotometric method has been developed for estimation of Perindopril erbumine &amp; Indapamide drug by AUC method. Quantitative determination of the drug was performed at wavelength range 208-214 nm and 239-244 nm for Perindopril erbumine &amp; Indapamide respectively. The linearity was established over the concentration range of 10-50 µg/ml for Perindopril erbumine and 1-5 µg/ml for Indapamide with correlation coefficient value of 0.999 for both the drugs. Precision studies showed that % relative standard deviation was within range of acceptable limits. The recovery study was found to be within range of 99-101%. The proposed method has been validated as per ICH guidelines.</p>
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