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
Hauptverfasser: 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
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container_title South African journal of botany
container_volume 149
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. 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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. 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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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source Elsevier ScienceDirect Journals Complete; EZB Electronic Journals Library
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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