Comparison of Quercetin Pharmacokinetics Following Oral Supplementation in Humans

:  The objective of the study was to investigate the absorption of quercetin aglycone in 18 healthy human subjects administered via the following oral carrier systems: suspension of quercetin (quercetin QU995 powder in Tang® and spring water), nutritional bars (First Strike™), and chews (RealFX™ Q‐P...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of food science 2012-11, Vol.77 (11), p.H231-H238
Hauptverfasser: Kaushik, Diksha, O'Fallon, Kevin, Clarkson, Priscilla M., Patrick Dunne, C., Conca, Karen R., Michniak-Kohn, Bozena
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page H238
container_issue 11
container_start_page H231
container_title Journal of food science
container_volume 77
creator Kaushik, Diksha
O'Fallon, Kevin
Clarkson, Priscilla M.
Patrick Dunne, C.
Conca, Karen R.
Michniak-Kohn, Bozena
description :  The objective of the study was to investigate the absorption of quercetin aglycone in 18 healthy human subjects administered via the following oral carrier systems: suspension of quercetin (quercetin QU995 powder in Tang® and spring water), nutritional bars (First Strike™), and chews (RealFX™ Q‐Plus™). Subjects were divided into 3 groups of 6 individuals each receiving 500 mg quercetin in one of the aforementioned formulations. Blood levels were monitored immediately pre‐ and for 32 h postadministration. The concentration of total quercetin in blood samples was determined by solid phase extraction followed by high‐performance liquid chromatography analysis. Pharmacokinetic parameters were determined by noncompartmental modeling using Kinetica software. The Cmax of quercetin was highest with RealFX™ Q‐Plus™ Chews (1051.9 ± 393.1 μg/L) achieved within 3.3 h as compared to that for First Strike™ Bars (698.1 ± 189.5 μg/L in 2.3 h) and Tang® suspension (354.4 ± 87.6 μg/L in 4.7 h). The results showed no statistically significant difference in quercetin absorption among groups due to high variability within groups receiving quercetin from same dosage form. This study represents the first comprehensive evaluation of quercetin absorption from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Practical Application:  The current study describes for the first time, comprehensive evaluation of quercetin PK in humans from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Owing to quercetin's potent antioxidant and anti‐inflammatory actions, quercetin is widely being used as a nutritional supplement. In order to maximize the bioavailability of quercetin for its use in efficacy studies, it is important to determine its ideal oral carrier system and route for its delivery. The current research unveils vital information about quercetin supplementation to the international community, especially to soldiers, athletes, and the dietary supplement industry.
doi_str_mv 10.1111/j.1750-3841.2012.02934.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1273337429</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2829180291</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5354-3eafa65b85c19804b8e7ba63467f81f3acfef2c8e98255cf7cc012cb29da23713</originalsourceid><addsrcrecordid>eNqNkUtP3DAUhS3UCobHX6giddNNUr9iO5tK1QwDrWgBAWrVjeUYGzwkcbATMfz7Oh06i26KN_aVv3Ou7j0AZAgWKJ2PqwLxEuZEUFRgiHABcUVosd4Bs-3HGzCDEOMcIcr3wH6MKzjVhO2CPUxgRSuKZuBy7tteBRd9l3mbXY4maDO4Lru4V6FV2j-4LtU6ZkvfNP7JdXfZeVBNdjX2fWNa0w1qcEmcJKdjq7p4CN5a1URz9HIfgJvl8fX8ND87P_ky_3yW65KUNCdGWcXKWpQaVQLSWhheK0Yo41YgS5S2xmItTCVwWWrLtU6D6hpXtwoTjsgB-LDx7YN_HE0cZOuiNk2jOuPHKBHmhBBO02b-jzLGUVoJTuj7f9CVH0OXBkkUhpVgQsBEiQ2lg48xGCv74FoVniWCckpIruQUhJyCkFNC8k9Ccp2k714ajHVrbrfCv5Ek4NMGeHKNeX61sfy6XFxNz2SQbwxcHMx6a6DCg2Sc8FL--H4iF4ufc_YLMfmN_AZi9q3F</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1220986880</pqid></control><display><type>article</type><title>Comparison of Quercetin Pharmacokinetics Following Oral Supplementation in Humans</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Kaushik, Diksha ; O'Fallon, Kevin ; Clarkson, Priscilla M. ; Patrick Dunne, C. ; Conca, Karen R. ; Michniak-Kohn, Bozena</creator><creatorcontrib>Kaushik, Diksha ; O'Fallon, Kevin ; Clarkson, Priscilla M. ; Patrick Dunne, C. ; Conca, Karen R. ; Michniak-Kohn, Bozena</creatorcontrib><description>:  The objective of the study was to investigate the absorption of quercetin aglycone in 18 healthy human subjects administered via the following oral carrier systems: suspension of quercetin (quercetin QU995 powder in Tang® and spring water), nutritional bars (First Strike™), and chews (RealFX™ Q‐Plus™). Subjects were divided into 3 groups of 6 individuals each receiving 500 mg quercetin in one of the aforementioned formulations. Blood levels were monitored immediately pre‐ and for 32 h postadministration. The concentration of total quercetin in blood samples was determined by solid phase extraction followed by high‐performance liquid chromatography analysis. Pharmacokinetic parameters were determined by noncompartmental modeling using Kinetica software. The Cmax of quercetin was highest with RealFX™ Q‐Plus™ Chews (1051.9 ± 393.1 μg/L) achieved within 3.3 h as compared to that for First Strike™ Bars (698.1 ± 189.5 μg/L in 2.3 h) and Tang® suspension (354.4 ± 87.6 μg/L in 4.7 h). The results showed no statistically significant difference in quercetin absorption among groups due to high variability within groups receiving quercetin from same dosage form. This study represents the first comprehensive evaluation of quercetin absorption from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Practical Application:  The current study describes for the first time, comprehensive evaluation of quercetin PK in humans from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Owing to quercetin's potent antioxidant and anti‐inflammatory actions, quercetin is widely being used as a nutritional supplement. In order to maximize the bioavailability of quercetin for its use in efficacy studies, it is important to determine its ideal oral carrier system and route for its delivery. The current research unveils vital information about quercetin supplementation to the international community, especially to soldiers, athletes, and the dietary supplement industry.</description><identifier>ISSN: 0022-1147</identifier><identifier>EISSN: 1750-3841</identifier><identifier>DOI: 10.1111/j.1750-3841.2012.02934.x</identifier><identifier>PMID: 23094941</identifier><identifier>CODEN: JFDSAZ</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Administration, Oral ; Adolescent ; Adult ; Antioxidants - administration &amp; dosage ; Antioxidants - pharmacokinetics ; Area Under Curve ; AUC ; Bars ; Biological Availability ; Blood ; buccal ; Calibration ; Carriers ; Chromatography ; Chromatography, High Pressure Liquid ; Cmax ; Comparative analysis ; Dietary Supplements ; Female ; Food products ; Food science ; Foods ; Fortified ; Human ; Humans ; Male ; Mathematical models ; Nutrition ; oral ; Powders - chemistry ; quercetin ; Quercetin - administration &amp; dosage ; Quercetin - blood ; Quercetin - pharmacokinetics ; Receiving ; Young Adult</subject><ispartof>Journal of food science, 2012-11, Vol.77 (11), p.H231-H238</ispartof><rights>2012 Institute of Food Technologists</rights><rights>Copyright Institute of Food Technologists Nov 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5354-3eafa65b85c19804b8e7ba63467f81f3acfef2c8e98255cf7cc012cb29da23713</citedby><cites>FETCH-LOGICAL-c5354-3eafa65b85c19804b8e7ba63467f81f3acfef2c8e98255cf7cc012cb29da23713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1750-3841.2012.02934.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1750-3841.2012.02934.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23094941$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaushik, Diksha</creatorcontrib><creatorcontrib>O'Fallon, Kevin</creatorcontrib><creatorcontrib>Clarkson, Priscilla M.</creatorcontrib><creatorcontrib>Patrick Dunne, C.</creatorcontrib><creatorcontrib>Conca, Karen R.</creatorcontrib><creatorcontrib>Michniak-Kohn, Bozena</creatorcontrib><title>Comparison of Quercetin Pharmacokinetics Following Oral Supplementation in Humans</title><title>Journal of food science</title><addtitle>J Food Sci</addtitle><description>:  The objective of the study was to investigate the absorption of quercetin aglycone in 18 healthy human subjects administered via the following oral carrier systems: suspension of quercetin (quercetin QU995 powder in Tang® and spring water), nutritional bars (First Strike™), and chews (RealFX™ Q‐Plus™). Subjects were divided into 3 groups of 6 individuals each receiving 500 mg quercetin in one of the aforementioned formulations. Blood levels were monitored immediately pre‐ and for 32 h postadministration. The concentration of total quercetin in blood samples was determined by solid phase extraction followed by high‐performance liquid chromatography analysis. Pharmacokinetic parameters were determined by noncompartmental modeling using Kinetica software. The Cmax of quercetin was highest with RealFX™ Q‐Plus™ Chews (1051.9 ± 393.1 μg/L) achieved within 3.3 h as compared to that for First Strike™ Bars (698.1 ± 189.5 μg/L in 2.3 h) and Tang® suspension (354.4 ± 87.6 μg/L in 4.7 h). The results showed no statistically significant difference in quercetin absorption among groups due to high variability within groups receiving quercetin from same dosage form. This study represents the first comprehensive evaluation of quercetin absorption from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Practical Application:  The current study describes for the first time, comprehensive evaluation of quercetin PK in humans from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Owing to quercetin's potent antioxidant and anti‐inflammatory actions, quercetin is widely being used as a nutritional supplement. In order to maximize the bioavailability of quercetin for its use in efficacy studies, it is important to determine its ideal oral carrier system and route for its delivery. The current research unveils vital information about quercetin supplementation to the international community, especially to soldiers, athletes, and the dietary supplement industry.</description><subject>Administration, Oral</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Antioxidants - administration &amp; dosage</subject><subject>Antioxidants - pharmacokinetics</subject><subject>Area Under Curve</subject><subject>AUC</subject><subject>Bars</subject><subject>Biological Availability</subject><subject>Blood</subject><subject>buccal</subject><subject>Calibration</subject><subject>Carriers</subject><subject>Chromatography</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Cmax</subject><subject>Comparative analysis</subject><subject>Dietary Supplements</subject><subject>Female</subject><subject>Food products</subject><subject>Food science</subject><subject>Foods</subject><subject>Fortified</subject><subject>Human</subject><subject>Humans</subject><subject>Male</subject><subject>Mathematical models</subject><subject>Nutrition</subject><subject>oral</subject><subject>Powders - chemistry</subject><subject>quercetin</subject><subject>Quercetin - administration &amp; dosage</subject><subject>Quercetin - blood</subject><subject>Quercetin - pharmacokinetics</subject><subject>Receiving</subject><subject>Young Adult</subject><issn>0022-1147</issn><issn>1750-3841</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtP3DAUhS3UCobHX6giddNNUr9iO5tK1QwDrWgBAWrVjeUYGzwkcbATMfz7Oh06i26KN_aVv3Ou7j0AZAgWKJ2PqwLxEuZEUFRgiHABcUVosd4Bs-3HGzCDEOMcIcr3wH6MKzjVhO2CPUxgRSuKZuBy7tteBRd9l3mbXY4maDO4Lru4V6FV2j-4LtU6ZkvfNP7JdXfZeVBNdjX2fWNa0w1qcEmcJKdjq7p4CN5a1URz9HIfgJvl8fX8ND87P_ky_3yW65KUNCdGWcXKWpQaVQLSWhheK0Yo41YgS5S2xmItTCVwWWrLtU6D6hpXtwoTjsgB-LDx7YN_HE0cZOuiNk2jOuPHKBHmhBBO02b-jzLGUVoJTuj7f9CVH0OXBkkUhpVgQsBEiQ2lg48xGCv74FoVniWCckpIruQUhJyCkFNC8k9Ccp2k714ajHVrbrfCv5Ek4NMGeHKNeX61sfy6XFxNz2SQbwxcHMx6a6DCg2Sc8FL--H4iF4ufc_YLMfmN_AZi9q3F</recordid><startdate>201211</startdate><enddate>201211</enddate><creator>Kaushik, Diksha</creator><creator>O'Fallon, Kevin</creator><creator>Clarkson, Priscilla M.</creator><creator>Patrick Dunne, C.</creator><creator>Conca, Karen R.</creator><creator>Michniak-Kohn, Bozena</creator><general>Blackwell Publishing Inc</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QR</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>201211</creationdate><title>Comparison of Quercetin Pharmacokinetics Following Oral Supplementation in Humans</title><author>Kaushik, Diksha ; O'Fallon, Kevin ; Clarkson, Priscilla M. ; Patrick Dunne, C. ; Conca, Karen R. ; Michniak-Kohn, Bozena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5354-3eafa65b85c19804b8e7ba63467f81f3acfef2c8e98255cf7cc012cb29da23713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Administration, Oral</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Antioxidants - administration &amp; dosage</topic><topic>Antioxidants - pharmacokinetics</topic><topic>Area Under Curve</topic><topic>AUC</topic><topic>Bars</topic><topic>Biological Availability</topic><topic>Blood</topic><topic>buccal</topic><topic>Calibration</topic><topic>Carriers</topic><topic>Chromatography</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Cmax</topic><topic>Comparative analysis</topic><topic>Dietary Supplements</topic><topic>Female</topic><topic>Food products</topic><topic>Food science</topic><topic>Foods</topic><topic>Fortified</topic><topic>Human</topic><topic>Humans</topic><topic>Male</topic><topic>Mathematical models</topic><topic>Nutrition</topic><topic>oral</topic><topic>Powders - chemistry</topic><topic>quercetin</topic><topic>Quercetin - administration &amp; dosage</topic><topic>Quercetin - blood</topic><topic>Quercetin - pharmacokinetics</topic><topic>Receiving</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaushik, Diksha</creatorcontrib><creatorcontrib>O'Fallon, Kevin</creatorcontrib><creatorcontrib>Clarkson, Priscilla M.</creatorcontrib><creatorcontrib>Patrick Dunne, C.</creatorcontrib><creatorcontrib>Conca, Karen R.</creatorcontrib><creatorcontrib>Michniak-Kohn, Bozena</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of food science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaushik, Diksha</au><au>O'Fallon, Kevin</au><au>Clarkson, Priscilla M.</au><au>Patrick Dunne, C.</au><au>Conca, Karen R.</au><au>Michniak-Kohn, Bozena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of Quercetin Pharmacokinetics Following Oral Supplementation in Humans</atitle><jtitle>Journal of food science</jtitle><addtitle>J Food Sci</addtitle><date>2012-11</date><risdate>2012</risdate><volume>77</volume><issue>11</issue><spage>H231</spage><epage>H238</epage><pages>H231-H238</pages><issn>0022-1147</issn><eissn>1750-3841</eissn><coden>JFDSAZ</coden><abstract>:  The objective of the study was to investigate the absorption of quercetin aglycone in 18 healthy human subjects administered via the following oral carrier systems: suspension of quercetin (quercetin QU995 powder in Tang® and spring water), nutritional bars (First Strike™), and chews (RealFX™ Q‐Plus™). Subjects were divided into 3 groups of 6 individuals each receiving 500 mg quercetin in one of the aforementioned formulations. Blood levels were monitored immediately pre‐ and for 32 h postadministration. The concentration of total quercetin in blood samples was determined by solid phase extraction followed by high‐performance liquid chromatography analysis. Pharmacokinetic parameters were determined by noncompartmental modeling using Kinetica software. The Cmax of quercetin was highest with RealFX™ Q‐Plus™ Chews (1051.9 ± 393.1 μg/L) achieved within 3.3 h as compared to that for First Strike™ Bars (698.1 ± 189.5 μg/L in 2.3 h) and Tang® suspension (354.4 ± 87.6 μg/L in 4.7 h). The results showed no statistically significant difference in quercetin absorption among groups due to high variability within groups receiving quercetin from same dosage form. This study represents the first comprehensive evaluation of quercetin absorption from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Practical Application:  The current study describes for the first time, comprehensive evaluation of quercetin PK in humans from quercetin fortified oral food products at doses commonly used for quercetin supplementation. Owing to quercetin's potent antioxidant and anti‐inflammatory actions, quercetin is widely being used as a nutritional supplement. In order to maximize the bioavailability of quercetin for its use in efficacy studies, it is important to determine its ideal oral carrier system and route for its delivery. The current research unveils vital information about quercetin supplementation to the international community, especially to soldiers, athletes, and the dietary supplement industry.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>23094941</pmid><doi>10.1111/j.1750-3841.2012.02934.x</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-1147
ispartof Journal of food science, 2012-11, Vol.77 (11), p.H231-H238
issn 0022-1147
1750-3841
language eng
recordid cdi_proquest_miscellaneous_1273337429
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Administration, Oral
Adolescent
Adult
Antioxidants - administration & dosage
Antioxidants - pharmacokinetics
Area Under Curve
AUC
Bars
Biological Availability
Blood
buccal
Calibration
Carriers
Chromatography
Chromatography, High Pressure Liquid
Cmax
Comparative analysis
Dietary Supplements
Female
Food products
Food science
Foods
Fortified
Human
Humans
Male
Mathematical models
Nutrition
oral
Powders - chemistry
quercetin
Quercetin - administration & dosage
Quercetin - blood
Quercetin - pharmacokinetics
Receiving
Young Adult
title Comparison of Quercetin Pharmacokinetics Following Oral Supplementation in Humans
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T03%3A31%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comparison%20of%20Quercetin%20Pharmacokinetics%20Following%20Oral%20Supplementation%20in%20Humans&rft.jtitle=Journal%20of%20food%20science&rft.au=Kaushik,%20Diksha&rft.date=2012-11&rft.volume=77&rft.issue=11&rft.spage=H231&rft.epage=H238&rft.pages=H231-H238&rft.issn=0022-1147&rft.eissn=1750-3841&rft.coden=JFDSAZ&rft_id=info:doi/10.1111/j.1750-3841.2012.02934.x&rft_dat=%3Cproquest_cross%3E2829180291%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1220986880&rft_id=info:pmid/23094941&rfr_iscdi=true