Development and validation of RP-HPLC based bioanalytical method for simultaneous estimation of curcumin and quercetin in rat's plasma
•RP-HPLC method for curcumin and quercetin was developed in rat plasma.•The developed method was validated as per ICH M10 guidelines.•Method was found linear in the concentration range of 2–10 µg/mL.•Recovery above 95% and% RSD less than 2 indicated about accuracy and precision of method.•Absence of...
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Veröffentlicht in: | South African journal of botany 2022-09, Vol.149, p.870-877 |
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creator | Khursheed, Rubiya Wadhwa, Sheetu Kumar, Bimlesh Gulati, Monica Gupta, Saurabh Chaitanya, MVNL Kumar, Deepak Jha, Niraj Kumar Gupta, Gaurav Prasher, Parteek Chellappan, Dinesh Kumar Dua, Kamal Singh, Sachin Kumar |
description | •RP-HPLC method for curcumin and quercetin was developed in rat plasma.•The developed method was validated as per ICH M10 guidelines.•Method was found linear in the concentration range of 2–10 µg/mL.•Recovery above 95% and% RSD less than 2 indicated about accuracy and precision of method.•Absence of interfering peaks at the retention times of curcumin and quercetin indicated method's specificity.
Curcumin (CUR) and quercetin (QUE) are the two important flavonoids that possess very good anti-inflammatory, anti-oxidant, antidiabetic, analgesic and anti-cancer activities. Reverse phase high performance liquid chromatography (RP-HPLC) was used to develop a bioanalytical method for simultaneous estimation of both the drugs in the rat's plasma. The method was further validated as per ICH M10 guidelines using C-18 reverse phase column. Fisetin was used as an internal standard. Gradient elution was carried out at a flow rate of 1 mL/min in acetonitrile (ACN) and 2% glacial acetic acid (GAA). The chromatograms of all three phytoconstituents were recorded at detection wavelength of 392 nm. The drugs were extracted from the plasma samples by using protein precipitation method. The retention times (Rts) of fisetin, QUE and CUR were found to be 4.2, 5.5 and 12.1 min respectively. The developed method was found to be linear in the range of 2–10 µg/mL with regression coefficient (r2) of 0.9998 and 0.9993 for QUE and CUR respectively. The percentage recovery of drug more than 95% and percentage relative standard deviation less than 2% among the replicate studies indicated that the method was accurate and precise. Limit of detection (LOD) and limit of quantification (LOQ) in plasma samples were found to be 0.18 and 0.54 µg/mL for QUE and 0.35 and 1 µg/mL for CUR respectively. Further, the stability studies were also carried out at freeze-thaw cycles, short term stability at room temperature. The developed method was found to be robust and passed all the parameters of validation and therefore can be used effectively for estimation of CUR and QUE in the rat plasma. |
doi_str_mv | 10.1016/j.sajb.2021.12.009 |
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Curcumin (CUR) and quercetin (QUE) are the two important flavonoids that possess very good anti-inflammatory, anti-oxidant, antidiabetic, analgesic and anti-cancer activities. Reverse phase high performance liquid chromatography (RP-HPLC) was used to develop a bioanalytical method for simultaneous estimation of both the drugs in the rat's plasma. The method was further validated as per ICH M10 guidelines using C-18 reverse phase column. Fisetin was used as an internal standard. Gradient elution was carried out at a flow rate of 1 mL/min in acetonitrile (ACN) and 2% glacial acetic acid (GAA). The chromatograms of all three phytoconstituents were recorded at detection wavelength of 392 nm. The drugs were extracted from the plasma samples by using protein precipitation method. The retention times (Rts) of fisetin, QUE and CUR were found to be 4.2, 5.5 and 12.1 min respectively. The developed method was found to be linear in the range of 2–10 µg/mL with regression coefficient (r2) of 0.9998 and 0.9993 for QUE and CUR respectively. The percentage recovery of drug more than 95% and percentage relative standard deviation less than 2% among the replicate studies indicated that the method was accurate and precise. Limit of detection (LOD) and limit of quantification (LOQ) in plasma samples were found to be 0.18 and 0.54 µg/mL for QUE and 0.35 and 1 µg/mL for CUR respectively. Further, the stability studies were also carried out at freeze-thaw cycles, short term stability at room temperature. The developed method was found to be robust and passed all the parameters of validation and therefore can be used effectively for estimation of CUR and QUE in the rat plasma.</description><identifier>ISSN: 0254-6299</identifier><identifier>DOI: 10.1016/j.sajb.2021.12.009</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>acetic acid ; acetonitrile ; ambient temperature ; analgesics ; antioxidants ; Bioanalytical method development ; chemical constituents of plants ; Curcumin ; detection limit ; freeze-thaw cycles ; Quercetin ; Rat plasma ; rats ; regression analysis ; reversed-phase high performance liquid chromatography ; RP-HPLC ; standard deviation ; wavelengths</subject><ispartof>South African journal of botany, 2022-09, Vol.149, p.870-877</ispartof><rights>2021 SAAB</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-a3a77b7cd24f583340ff986cb6efb2fcee204853abedc232f365abd17804597b3</citedby><cites>FETCH-LOGICAL-c377t-a3a77b7cd24f583340ff986cb6efb2fcee204853abedc232f365abd17804597b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0254629921005275$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Khursheed, Rubiya</creatorcontrib><creatorcontrib>Wadhwa, Sheetu</creatorcontrib><creatorcontrib>Kumar, Bimlesh</creatorcontrib><creatorcontrib>Gulati, Monica</creatorcontrib><creatorcontrib>Gupta, Saurabh</creatorcontrib><creatorcontrib>Chaitanya, MVNL</creatorcontrib><creatorcontrib>Kumar, Deepak</creatorcontrib><creatorcontrib>Jha, Niraj Kumar</creatorcontrib><creatorcontrib>Gupta, Gaurav</creatorcontrib><creatorcontrib>Prasher, Parteek</creatorcontrib><creatorcontrib>Chellappan, Dinesh Kumar</creatorcontrib><creatorcontrib>Dua, Kamal</creatorcontrib><creatorcontrib>Singh, Sachin Kumar</creatorcontrib><title>Development and validation of RP-HPLC based bioanalytical method for simultaneous estimation of curcumin and quercetin in rat's plasma</title><title>South African journal of botany</title><description>•RP-HPLC method for curcumin and quercetin was developed in rat plasma.•The developed method was validated as per ICH M10 guidelines.•Method was found linear in the concentration range of 2–10 µg/mL.•Recovery above 95% and% RSD less than 2 indicated about accuracy and precision of method.•Absence of interfering peaks at the retention times of curcumin and quercetin indicated method's specificity.
Curcumin (CUR) and quercetin (QUE) are the two important flavonoids that possess very good anti-inflammatory, anti-oxidant, antidiabetic, analgesic and anti-cancer activities. Reverse phase high performance liquid chromatography (RP-HPLC) was used to develop a bioanalytical method for simultaneous estimation of both the drugs in the rat's plasma. The method was further validated as per ICH M10 guidelines using C-18 reverse phase column. Fisetin was used as an internal standard. Gradient elution was carried out at a flow rate of 1 mL/min in acetonitrile (ACN) and 2% glacial acetic acid (GAA). The chromatograms of all three phytoconstituents were recorded at detection wavelength of 392 nm. The drugs were extracted from the plasma samples by using protein precipitation method. The retention times (Rts) of fisetin, QUE and CUR were found to be 4.2, 5.5 and 12.1 min respectively. The developed method was found to be linear in the range of 2–10 µg/mL with regression coefficient (r2) of 0.9998 and 0.9993 for QUE and CUR respectively. The percentage recovery of drug more than 95% and percentage relative standard deviation less than 2% among the replicate studies indicated that the method was accurate and precise. Limit of detection (LOD) and limit of quantification (LOQ) in plasma samples were found to be 0.18 and 0.54 µg/mL for QUE and 0.35 and 1 µg/mL for CUR respectively. Further, the stability studies were also carried out at freeze-thaw cycles, short term stability at room temperature. The developed method was found to be robust and passed all the parameters of validation and therefore can be used effectively for estimation of CUR and QUE in the rat plasma.</description><subject>acetic acid</subject><subject>acetonitrile</subject><subject>ambient temperature</subject><subject>analgesics</subject><subject>antioxidants</subject><subject>Bioanalytical method development</subject><subject>chemical constituents of plants</subject><subject>Curcumin</subject><subject>detection limit</subject><subject>freeze-thaw cycles</subject><subject>Quercetin</subject><subject>Rat plasma</subject><subject>rats</subject><subject>regression analysis</subject><subject>reversed-phase high performance liquid chromatography</subject><subject>RP-HPLC</subject><subject>standard deviation</subject><subject>wavelengths</subject><issn>0254-6299</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kM1qGzEUhWfRQlwnL9CVdu1mpvqZX-gmOE0dMNSEdC2upCsqoxk5ksaQF8hzZ1yHLgsXLhfOOdzzFcVnRitGWfvtUCU4qIpTzirGK0qHD8WK8qYuWz4MV8WnlA6UMsF7vipe7_CEPhxHnDKByZATeGcguzCRYMnjvtzudxuiIKEhygWYwL9kp8GTEfOfYIgNkSQ3zj7DhGFOBFN2478EPUc9j276G_48Y9SYl2uZCPlLIkcPaYTr4qMFn_Dmfa-L3_c_njbbcvfr58Pmdldq0XW5BAFdpzpteG2bXoiaWjv0rVYtWsWtRuS07hsBCo3mglvRNqAM63paN0OnxLr4esk9xrA8k7IcXdLo_eV3yVvRtp1ommaR8otUx5BSRCuPcekVXySj8gxaHuQZtDyDlozLBfRi-n4x4VLi5DDKpB1OGo2LqLM0wf3P_gYpMYvR</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Khursheed, Rubiya</creator><creator>Wadhwa, Sheetu</creator><creator>Kumar, Bimlesh</creator><creator>Gulati, Monica</creator><creator>Gupta, Saurabh</creator><creator>Chaitanya, MVNL</creator><creator>Kumar, Deepak</creator><creator>Jha, Niraj Kumar</creator><creator>Gupta, Gaurav</creator><creator>Prasher, Parteek</creator><creator>Chellappan, Dinesh Kumar</creator><creator>Dua, Kamal</creator><creator>Singh, Sachin Kumar</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20220901</creationdate><title>Development and validation of RP-HPLC based bioanalytical method for simultaneous estimation of curcumin and quercetin in rat's plasma</title><author>Khursheed, Rubiya ; Wadhwa, Sheetu ; Kumar, Bimlesh ; Gulati, Monica ; Gupta, Saurabh ; Chaitanya, MVNL ; Kumar, Deepak ; Jha, Niraj Kumar ; Gupta, Gaurav ; Prasher, Parteek ; Chellappan, Dinesh Kumar ; Dua, Kamal ; Singh, Sachin Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-a3a77b7cd24f583340ff986cb6efb2fcee204853abedc232f365abd17804597b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>acetic acid</topic><topic>acetonitrile</topic><topic>ambient temperature</topic><topic>analgesics</topic><topic>antioxidants</topic><topic>Bioanalytical method development</topic><topic>chemical constituents of plants</topic><topic>Curcumin</topic><topic>detection limit</topic><topic>freeze-thaw cycles</topic><topic>Quercetin</topic><topic>Rat plasma</topic><topic>rats</topic><topic>regression analysis</topic><topic>reversed-phase high performance liquid chromatography</topic><topic>RP-HPLC</topic><topic>standard deviation</topic><topic>wavelengths</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khursheed, Rubiya</creatorcontrib><creatorcontrib>Wadhwa, Sheetu</creatorcontrib><creatorcontrib>Kumar, Bimlesh</creatorcontrib><creatorcontrib>Gulati, Monica</creatorcontrib><creatorcontrib>Gupta, Saurabh</creatorcontrib><creatorcontrib>Chaitanya, MVNL</creatorcontrib><creatorcontrib>Kumar, Deepak</creatorcontrib><creatorcontrib>Jha, Niraj Kumar</creatorcontrib><creatorcontrib>Gupta, Gaurav</creatorcontrib><creatorcontrib>Prasher, Parteek</creatorcontrib><creatorcontrib>Chellappan, Dinesh Kumar</creatorcontrib><creatorcontrib>Dua, Kamal</creatorcontrib><creatorcontrib>Singh, Sachin Kumar</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>South African journal of botany</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khursheed, Rubiya</au><au>Wadhwa, Sheetu</au><au>Kumar, Bimlesh</au><au>Gulati, Monica</au><au>Gupta, Saurabh</au><au>Chaitanya, MVNL</au><au>Kumar, Deepak</au><au>Jha, Niraj Kumar</au><au>Gupta, Gaurav</au><au>Prasher, Parteek</au><au>Chellappan, Dinesh Kumar</au><au>Dua, Kamal</au><au>Singh, Sachin Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and validation of RP-HPLC based bioanalytical method for simultaneous estimation of curcumin and quercetin in rat's plasma</atitle><jtitle>South African journal of botany</jtitle><date>2022-09-01</date><risdate>2022</risdate><volume>149</volume><spage>870</spage><epage>877</epage><pages>870-877</pages><issn>0254-6299</issn><abstract>•RP-HPLC method for curcumin and quercetin was developed in rat plasma.•The developed method was validated as per ICH M10 guidelines.•Method was found linear in the concentration range of 2–10 µg/mL.•Recovery above 95% and% RSD less than 2 indicated about accuracy and precision of method.•Absence of interfering peaks at the retention times of curcumin and quercetin indicated method's specificity.
Curcumin (CUR) and quercetin (QUE) are the two important flavonoids that possess very good anti-inflammatory, anti-oxidant, antidiabetic, analgesic and anti-cancer activities. Reverse phase high performance liquid chromatography (RP-HPLC) was used to develop a bioanalytical method for simultaneous estimation of both the drugs in the rat's plasma. The method was further validated as per ICH M10 guidelines using C-18 reverse phase column. Fisetin was used as an internal standard. Gradient elution was carried out at a flow rate of 1 mL/min in acetonitrile (ACN) and 2% glacial acetic acid (GAA). The chromatograms of all three phytoconstituents were recorded at detection wavelength of 392 nm. The drugs were extracted from the plasma samples by using protein precipitation method. The retention times (Rts) of fisetin, QUE and CUR were found to be 4.2, 5.5 and 12.1 min respectively. The developed method was found to be linear in the range of 2–10 µg/mL with regression coefficient (r2) of 0.9998 and 0.9993 for QUE and CUR respectively. The percentage recovery of drug more than 95% and percentage relative standard deviation less than 2% among the replicate studies indicated that the method was accurate and precise. Limit of detection (LOD) and limit of quantification (LOQ) in plasma samples were found to be 0.18 and 0.54 µg/mL for QUE and 0.35 and 1 µg/mL for CUR respectively. Further, the stability studies were also carried out at freeze-thaw cycles, short term stability at room temperature. The developed method was found to be robust and passed all the parameters of validation and therefore can be used effectively for estimation of CUR and QUE in the rat plasma.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.sajb.2021.12.009</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | acetic acid acetonitrile ambient temperature analgesics antioxidants Bioanalytical method development chemical constituents of plants Curcumin detection limit freeze-thaw cycles Quercetin Rat plasma rats regression analysis reversed-phase high performance liquid chromatography RP-HPLC standard deviation wavelengths |
title | Development and validation of RP-HPLC based bioanalytical method for simultaneous estimation of curcumin and quercetin in rat's plasma |
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