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Development and Validation of a RP-UHPLC Method for estimation of Gliclazide loaded Microsphere
Objective: The objective of the current work is to develop and validate a simple yet effective, efficient and reproducible RP-UHPLC method for the determination of Gilcazide loaded in a microsphere formulation. Methods: The chromatographic analysis was carried out on Thermo Scientific (Dionex Ultra...
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Published in: | Research journal of pharmacy and technology 2022-02, Vol.15 (2), p.773-778 |
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creator | Ahmed, Abdul Baquee Bordoloi, Ripunjoy Bhattacharya, Kunal |
description | Objective: The objective of the current work is to develop and validate a simple yet effective, efficient and reproducible RP-UHPLC method for the determination of Gilcazide loaded in a microsphere formulation. Methods: The chromatographic analysis was carried out on Thermo Scientific (Dionex Ultra 3000plus) UHPLC using a stainless steel YMC C8 column (25cm × 4mm) packed with endcapped octylsilane bonded to porous silica (4µm) in isocratic elution mode using phosphate buffer pH 3.4 and HPLC grade acetonitrile in the ratio of 20: 80 (v/v) as eluent. The flow rate was adjusted as 1ml/min and eluent was detected at 230 nm. The retention time was observed at 1.9 min. Results: The linear dynamic range for the developed UHPLC method was found in the concentration range of 2-10µg/ml and percentage recovery was in the range of 94%-98%. Drug Entrapment Efficiency Data of Gliclazide loaded microsphere was found to be 93.72% Conclusion: In this RP–UHPLC method, the linearity was within the range of 2–10μg/mL and the validation parameters were within the limits was performed as per ICH guidelines. The % Drug entrapment Efficiency of the Gliclazide loaded microsphere was found to be 93.72 % which was satisfactory. |
doi_str_mv | 10.52711/0974-360X.2022.00129 |
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Methods: The chromatographic analysis was carried out on Thermo Scientific (Dionex Ultra 3000plus) UHPLC using a stainless steel YMC C8 column (25cm × 4mm) packed with endcapped octylsilane bonded to porous silica (4µm) in isocratic elution mode using phosphate buffer pH 3.4 and HPLC grade acetonitrile in the ratio of 20: 80 (v/v) as eluent. The flow rate was adjusted as 1ml/min and eluent was detected at 230 nm. The retention time was observed at 1.9 min. Results: The linear dynamic range for the developed UHPLC method was found in the concentration range of 2-10µg/ml and percentage recovery was in the range of 94%-98%. Drug Entrapment Efficiency Data of Gliclazide loaded microsphere was found to be 93.72% Conclusion: In this RP–UHPLC method, the linearity was within the range of 2–10μg/mL and the validation parameters were within the limits was performed as per ICH guidelines. The % Drug entrapment Efficiency of the Gliclazide loaded microsphere was found to be 93.72 % which was satisfactory.</description><identifier>ISSN: 0974-3618</identifier><identifier>EISSN: 0974-360X</identifier><identifier>EISSN: 0974-306X</identifier><identifier>DOI: 10.52711/0974-360X.2022.00129</identifier><language>eng</language><publisher>Raipur: A&V Publications</publisher><subject>Chromatography ; Diabetes ; Efficiency ; Fourier transforms ; Membrane filters ; Particle size ; Stainless steel</subject><ispartof>Research journal of pharmacy and technology, 2022-02, Vol.15 (2), p.773-778</ispartof><rights>Copyright A&V Publications Feb 2022</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c144t-e8846b74cfe1feab934b133cbdf65c2fd6d5c935a0255cb0a7e946bb172e04c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Ahmed, Abdul Baquee</creatorcontrib><creatorcontrib>Bordoloi, Ripunjoy</creatorcontrib><creatorcontrib>Bhattacharya, Kunal</creatorcontrib><title>Development and Validation of a RP-UHPLC Method for estimation of Gliclazide loaded Microsphere</title><title>Research journal of pharmacy and technology</title><description>Objective: The objective of the current work is to develop and validate a simple yet effective, efficient and reproducible RP-UHPLC method for the determination of Gilcazide loaded in a microsphere formulation. Methods: The chromatographic analysis was carried out on Thermo Scientific (Dionex Ultra 3000plus) UHPLC using a stainless steel YMC C8 column (25cm × 4mm) packed with endcapped octylsilane bonded to porous silica (4µm) in isocratic elution mode using phosphate buffer pH 3.4 and HPLC grade acetonitrile in the ratio of 20: 80 (v/v) as eluent. The flow rate was adjusted as 1ml/min and eluent was detected at 230 nm. The retention time was observed at 1.9 min. Results: The linear dynamic range for the developed UHPLC method was found in the concentration range of 2-10µg/ml and percentage recovery was in the range of 94%-98%. Drug Entrapment Efficiency Data of Gliclazide loaded microsphere was found to be 93.72% Conclusion: In this RP–UHPLC method, the linearity was within the range of 2–10μg/mL and the validation parameters were within the limits was performed as per ICH guidelines. The % Drug entrapment Efficiency of the Gliclazide loaded microsphere was found to be 93.72 % which was satisfactory.</description><subject>Chromatography</subject><subject>Diabetes</subject><subject>Efficiency</subject><subject>Fourier transforms</subject><subject>Membrane filters</subject><subject>Particle size</subject><subject>Stainless steel</subject><issn>0974-3618</issn><issn>0974-360X</issn><issn>0974-306X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNo9kG9LwzAQxoMoOOY-ghDwdWf-ts1LmboJGw6Z4ruQJhfW0TU17QT99Lab7N7ccTx399wPoVtKppJllN4TlYmEp-RzyghjU0IoUxdodG5fnmuaX6NJ2-5IH2kumchHSD_CN1Sh2UPdYVM7_GGq0pmuDDUOHhv8tk7eF-vlDK-g2waHfYgY2q7cnzXzqrSV-S0d4CoYBw6vShtD22whwg268qZqYfKfx2jz_LSZLZLl6_xl9rBMLBWiSyDPRVpkwnqgHkyhuCgo57ZwPpWWeZc6aRWXhjApbUFMBqofKGjGgAjLx-jutLaJ4evQ-9O7cIh1f1GzVJBMZUrQXiVPqsFeG8HrJvaPxB9NiT7S1AMqPWDTA019pMn_AJSUZ9Q</recordid><startdate>20220201</startdate><enddate>20220201</enddate><creator>Ahmed, Abdul Baquee</creator><creator>Bordoloi, Ripunjoy</creator><creator>Bhattacharya, Kunal</creator><general>A&V Publications</general><scope>AAYXX</scope><scope>CITATION</scope><scope>04Q</scope><scope>04S</scope><scope>04W</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20220201</creationdate><title>Development and Validation of a RP-UHPLC Method for estimation of Gliclazide loaded Microsphere</title><author>Ahmed, Abdul Baquee ; Bordoloi, Ripunjoy ; Bhattacharya, Kunal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c144t-e8846b74cfe1feab934b133cbdf65c2fd6d5c935a0255cb0a7e946bb172e04c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Chromatography</topic><topic>Diabetes</topic><topic>Efficiency</topic><topic>Fourier transforms</topic><topic>Membrane filters</topic><topic>Particle size</topic><topic>Stainless steel</topic><toplevel>online_resources</toplevel><creatorcontrib>Ahmed, Abdul Baquee</creatorcontrib><creatorcontrib>Bordoloi, Ripunjoy</creatorcontrib><creatorcontrib>Bhattacharya, Kunal</creatorcontrib><collection>CrossRef</collection><collection>India Database</collection><collection>India Database: Business</collection><collection>India Database: Science & Technology</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Research journal of pharmacy and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmed, Abdul Baquee</au><au>Bordoloi, Ripunjoy</au><au>Bhattacharya, Kunal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and Validation of a RP-UHPLC Method for estimation of Gliclazide loaded Microsphere</atitle><jtitle>Research journal of pharmacy and technology</jtitle><date>2022-02-01</date><risdate>2022</risdate><volume>15</volume><issue>2</issue><spage>773</spage><epage>778</epage><pages>773-778</pages><issn>0974-3618</issn><eissn>0974-360X</eissn><eissn>0974-306X</eissn><abstract>Objective: The objective of the current work is to develop and validate a simple yet effective, efficient and reproducible RP-UHPLC method for the determination of Gilcazide loaded in a microsphere formulation. Methods: The chromatographic analysis was carried out on Thermo Scientific (Dionex Ultra 3000plus) UHPLC using a stainless steel YMC C8 column (25cm × 4mm) packed with endcapped octylsilane bonded to porous silica (4µm) in isocratic elution mode using phosphate buffer pH 3.4 and HPLC grade acetonitrile in the ratio of 20: 80 (v/v) as eluent. The flow rate was adjusted as 1ml/min and eluent was detected at 230 nm. The retention time was observed at 1.9 min. Results: The linear dynamic range for the developed UHPLC method was found in the concentration range of 2-10µg/ml and percentage recovery was in the range of 94%-98%. Drug Entrapment Efficiency Data of Gliclazide loaded microsphere was found to be 93.72% Conclusion: In this RP–UHPLC method, the linearity was within the range of 2–10μg/mL and the validation parameters were within the limits was performed as per ICH guidelines. The % Drug entrapment Efficiency of the Gliclazide loaded microsphere was found to be 93.72 % which was satisfactory.</abstract><cop>Raipur</cop><pub>A&V Publications</pub><doi>10.52711/0974-360X.2022.00129</doi><tpages>6</tpages></addata></record> |
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subjects | Chromatography Diabetes Efficiency Fourier transforms Membrane filters Particle size Stainless steel |
title | Development and Validation of a RP-UHPLC Method for estimation of Gliclazide loaded Microsphere |
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