Increased Oral Bioavailability of Resveratrol by Its Encapsulation in Casein Nanoparticles
Resveratrol is a naturally occurring polyphenol that provides several health benefits including cardioprotection and cancer prevention. However, its biological activity is limited by a poor bioavailability when taken orally. The aim of this work was to evaluate the capability of casein nanoparticles...
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description | Resveratrol is a naturally occurring polyphenol that provides several health benefits including cardioprotection and cancer prevention. However, its biological activity is limited by a poor bioavailability when taken orally. The aim of this work was to evaluate the capability of casein nanoparticles as oral carriers for resveratrol. Nanoparticles were prepared by a coacervation process, purified and dried by spray-drying. The mean size of nanoparticles was around 200 nm with a resveratrol payload close to 30 μg/mg nanoparticle. In vitro studies demonstrated that the resveratrol release from casein nanoparticles was not affected by the pH conditions and followed a zero-order kinetic. When nanoparticles were administered orally to rats, they remained within the gut, displaying an important capability to reach the intestinal epithelium. No evidence of nanoparticle "translocation" were observed. The resveratrol plasma levels were high and sustained for at least 8 h with a similar profile to that observed for the presence of the major metabolite in plasma. The oral bioavailability of resveratrol when loaded in casein nanoparticles was calculated to be 26.5%, 10 times higher than when the polyphenol was administered as oral solution. Finally, a good correlation between in vitro and in vivo data was observed. |
doi_str_mv | 10.3390/ijms19092816 |
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However, its biological activity is limited by a poor bioavailability when taken orally. The aim of this work was to evaluate the capability of casein nanoparticles as oral carriers for resveratrol. Nanoparticles were prepared by a coacervation process, purified and dried by spray-drying. The mean size of nanoparticles was around 200 nm with a resveratrol payload close to 30 μg/mg nanoparticle. In vitro studies demonstrated that the resveratrol release from casein nanoparticles was not affected by the pH conditions and followed a zero-order kinetic. When nanoparticles were administered orally to rats, they remained within the gut, displaying an important capability to reach the intestinal epithelium. No evidence of nanoparticle "translocation" were observed. The resveratrol plasma levels were high and sustained for at least 8 h with a similar profile to that observed for the presence of the major metabolite in plasma. The oral bioavailability of resveratrol when loaded in casein nanoparticles was calculated to be 26.5%, 10 times higher than when the polyphenol was administered as oral solution. Finally, a good correlation between in vitro and in vivo data was observed.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms19092816</identifier><identifier>PMID: 30231546</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Administration, Oral ; Animals ; Anticarcinogenic Agents - administration & dosage ; Anticarcinogenic Agents - pharmacokinetics ; Bioavailability ; Biological activity ; Biological Availability ; Cancer ; Cardiotonic Agents - administration & dosage ; Cardiotonic Agents - pharmacokinetics ; Casein ; Caseins - chemistry ; Coacervation ; Drug Carriers - chemistry ; Drug delivery systems ; Drying ; Epithelium ; Food ; Functional foods & nutraceuticals ; Intestine ; Kinases ; Male ; Metabolism ; Metabolites ; Nanoparticles ; Nanoparticles - chemistry ; Nanoparticles - ultrastructure ; Nutrition research ; Plasma levels ; Polyphenols ; Rats, Wistar ; Resveratrol ; Resveratrol - administration & dosage ; Resveratrol - pharmacokinetics ; Scanning electron microscopy</subject><ispartof>International journal of molecular sciences, 2018-09, Vol.19 (9), p.2816</ispartof><rights>2018. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2018 by the authors. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-52b6233c2141849d07804f433c0d1c2cf6df9b04b67f9efc3f47c2ff01c2e1d83</citedby><cites>FETCH-LOGICAL-c478t-52b6233c2141849d07804f433c0d1c2cf6df9b04b67f9efc3f47c2ff01c2e1d83</cites><orcidid>0000-0001-9687-3436 ; 0000-0002-3517-9077 ; 0000-0003-3710-0438 ; 0000-0002-5637-7187 ; 0000-0002-9279-2249 ; 0000-0001-8008-976X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163610/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163610/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30231546$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peñalva, Rebeca</creatorcontrib><creatorcontrib>Morales, Jorge</creatorcontrib><creatorcontrib>González-Navarro, Carlos J</creatorcontrib><creatorcontrib>Larrañeta, Eneko</creatorcontrib><creatorcontrib>Quincoces, Gemma</creatorcontrib><creatorcontrib>Peñuelas, Ivan</creatorcontrib><creatorcontrib>Irache, Juan M</creatorcontrib><title>Increased Oral Bioavailability of Resveratrol by Its Encapsulation in Casein Nanoparticles</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Resveratrol is a naturally occurring polyphenol that provides several health benefits including cardioprotection and cancer prevention. However, its biological activity is limited by a poor bioavailability when taken orally. The aim of this work was to evaluate the capability of casein nanoparticles as oral carriers for resveratrol. Nanoparticles were prepared by a coacervation process, purified and dried by spray-drying. The mean size of nanoparticles was around 200 nm with a resveratrol payload close to 30 μg/mg nanoparticle. In vitro studies demonstrated that the resveratrol release from casein nanoparticles was not affected by the pH conditions and followed a zero-order kinetic. When nanoparticles were administered orally to rats, they remained within the gut, displaying an important capability to reach the intestinal epithelium. No evidence of nanoparticle "translocation" were observed. The resveratrol plasma levels were high and sustained for at least 8 h with a similar profile to that observed for the presence of the major metabolite in plasma. The oral bioavailability of resveratrol when loaded in casein nanoparticles was calculated to be 26.5%, 10 times higher than when the polyphenol was administered as oral solution. Finally, a good correlation between in vitro and in vivo data was observed.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Anticarcinogenic Agents - administration & dosage</subject><subject>Anticarcinogenic Agents - pharmacokinetics</subject><subject>Bioavailability</subject><subject>Biological activity</subject><subject>Biological Availability</subject><subject>Cancer</subject><subject>Cardiotonic Agents - administration & dosage</subject><subject>Cardiotonic Agents - pharmacokinetics</subject><subject>Casein</subject><subject>Caseins - chemistry</subject><subject>Coacervation</subject><subject>Drug Carriers - chemistry</subject><subject>Drug delivery systems</subject><subject>Drying</subject><subject>Epithelium</subject><subject>Food</subject><subject>Functional foods & nutraceuticals</subject><subject>Intestine</subject><subject>Kinases</subject><subject>Male</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Nanoparticles</subject><subject>Nanoparticles - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peñalva, Rebeca</au><au>Morales, Jorge</au><au>González-Navarro, Carlos J</au><au>Larrañeta, Eneko</au><au>Quincoces, Gemma</au><au>Peñuelas, Ivan</au><au>Irache, Juan M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased Oral Bioavailability of Resveratrol by Its Encapsulation in Casein Nanoparticles</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2018-09-18</date><risdate>2018</risdate><volume>19</volume><issue>9</issue><spage>2816</spage><pages>2816-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Resveratrol is a naturally occurring polyphenol that provides several health benefits including cardioprotection and cancer prevention. However, its biological activity is limited by a poor bioavailability when taken orally. The aim of this work was to evaluate the capability of casein nanoparticles as oral carriers for resveratrol. Nanoparticles were prepared by a coacervation process, purified and dried by spray-drying. The mean size of nanoparticles was around 200 nm with a resveratrol payload close to 30 μg/mg nanoparticle. In vitro studies demonstrated that the resveratrol release from casein nanoparticles was not affected by the pH conditions and followed a zero-order kinetic. When nanoparticles were administered orally to rats, they remained within the gut, displaying an important capability to reach the intestinal epithelium. No evidence of nanoparticle "translocation" were observed. The resveratrol plasma levels were high and sustained for at least 8 h with a similar profile to that observed for the presence of the major metabolite in plasma. The oral bioavailability of resveratrol when loaded in casein nanoparticles was calculated to be 26.5%, 10 times higher than when the polyphenol was administered as oral solution. Finally, a good correlation between in vitro and in vivo data was observed.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>30231546</pmid><doi>10.3390/ijms19092816</doi><orcidid>https://orcid.org/0000-0001-9687-3436</orcidid><orcidid>https://orcid.org/0000-0002-3517-9077</orcidid><orcidid>https://orcid.org/0000-0003-3710-0438</orcidid><orcidid>https://orcid.org/0000-0002-5637-7187</orcidid><orcidid>https://orcid.org/0000-0002-9279-2249</orcidid><orcidid>https://orcid.org/0000-0001-8008-976X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals Anticarcinogenic Agents - administration & dosage Anticarcinogenic Agents - pharmacokinetics Bioavailability Biological activity Biological Availability Cancer Cardiotonic Agents - administration & dosage Cardiotonic Agents - pharmacokinetics Casein Caseins - chemistry Coacervation Drug Carriers - chemistry Drug delivery systems Drying Epithelium Food Functional foods & nutraceuticals Intestine Kinases Male Metabolism Metabolites Nanoparticles Nanoparticles - chemistry Nanoparticles - ultrastructure Nutrition research Plasma levels Polyphenols Rats, Wistar Resveratrol Resveratrol - administration & dosage Resveratrol - pharmacokinetics Scanning electron microscopy |
title | Increased Oral Bioavailability of Resveratrol by Its Encapsulation in Casein Nanoparticles |
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