Formation and functional attributes of electrostatic complexes involving casein and anionic polysaccharides: An approach to enhance oral absorption of lycopene in rats in vivo

•Microencapsulation of lycopene was carried out by coacervation method.•Casein and Gum tragacanth was used as coating material.•The microencapsules fabricated at 1:2 of Gt:Cas were also revealed the highest loading capacity and maximum coacervates yield.•Cumulative lycopene release was estimated 86....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of biological macromolecules 2016-12, Vol.93 (Pt A), p.746-756
Hauptverfasser: Jain, Ashay, Thakur, Deepika, Ghoshal, Gargi, Katare, O.P., Singh, Bhupinder, Shivhare, U.S.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 756
container_issue Pt A
container_start_page 746
container_title International journal of biological macromolecules
container_volume 93
creator Jain, Ashay
Thakur, Deepika
Ghoshal, Gargi
Katare, O.P.
Singh, Bhupinder
Shivhare, U.S.
description •Microencapsulation of lycopene was carried out by coacervation method.•Casein and Gum tragacanth was used as coating material.•The microencapsules fabricated at 1:2 of Gt:Cas were also revealed the highest loading capacity and maximum coacervates yield.•Cumulative lycopene release was estimated 86.34±2.69% from microencapsulated formulations at the end of 24th h.•The stability of lycopene in that formulation in term of % residual content were studied for three months. The current work entails a novel strategy of formulating the microparticles of lycopene solely using rational blends of biopolymers without using equipment-intensive techniques. The study is intended to enhance oral bioavailability of lycopene by controlling its release from micro-formulation and facilitating its absorption though lymphatic pathways. Considering the minimum particle size, maximum entrapment efficiency and loading capacity, the amounts of casein (i.e., protein) and gum tragacanth (i.e., polysaccharide) were selected as the critical factors for formulation of microparticles. Complex formation and electrostatic interaction was confirmed by Fourier transform infra red (FTIR) spectra. Size and surface properties of microparticles were studied using scanning electron microscopy (SEM). The optimized formulation (mean particle size: ∼130μm; % entrapment efficiency: ∼67% and loading capacity: ∼71%) designated noticeable improvement in lycopene release profile (over 80% in 24h). Increment in the values of Cmax (2.22-fold) and AUC (1.97-fold) further indicated noteworthy augmentation in the rate and extent of bioavailability by the microparticles formulation compared to plain lycopene. The resulting formulation was found to be quite stable all through two months of study episode. The resultant microparticles formulation was evaluated for antioxidant activity and tested for their effectiveness in self life enhancement of vegetable oil by calculating peroxide value under temperature and storage condition. Encapsulation strongly increased the stability of micronutrients. The current investigations, therefore, report the successful development of biopolymeric microparticles with improved bioavailability potential of lycopene.
doi_str_mv 10.1016/j.ijbiomac.2016.08.071
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1835357063</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0141813016307887</els_id><sourcerecordid>1835357063</sourcerecordid><originalsourceid>FETCH-LOGICAL-c368t-6e17bf67f2b8c59dea754a827f26ef03fefcbc7baf542972029ace484f3e5b523</originalsourceid><addsrcrecordid>eNqFUU1v1DAQtRAVXQp_ofKRS4Id58PLiaqiLVIlLuVsOc6Y9Sqxg-1E7K_iLzJhW66cRjPz5r2ZeYRcc1ZyxtuPx9IdexcmbcoK85LJknX8Fdlx2e0Lxph4TXaM17yQXLBL8jalI1bbhss35LLqmq6pRb0jv-9CnHR2wVPtB2oXb7ZEj1TnHF2_ZEg0WAojmBxDyog11IRpHuEXtpxfw7g6_4MancCdWbRHCoTNYTwlbcxBRzdA-kRvsD_PMWhzoDlQ8AftDdAQN70-hTj_3QT1xpMJM3hAARp13oTo6tbwjlxYPSZ4_xyvyPe7L0-3D8Xjt_uvtzePhRGtzEULvOtt29mql6bZD6DxXi0rLLRgmbBgTW-6XtumrvZdxaq9NlDL2gpo-qYSV-TDmRe3_blAympyycA4ag9hSYpL0YimY61AaHuGGvxPimDVHN2k40lxpjaz1FG9mKU2sxSTCs3CwetnjaWfYPg39uIOAj6fAYCXrg6iSsYBfmxwEe1QQ3D_0_gDkyiu7A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1835357063</pqid></control><display><type>article</type><title>Formation and functional attributes of electrostatic complexes involving casein and anionic polysaccharides: An approach to enhance oral absorption of lycopene in rats in vivo</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Jain, Ashay ; Thakur, Deepika ; Ghoshal, Gargi ; Katare, O.P. ; Singh, Bhupinder ; Shivhare, U.S.</creator><creatorcontrib>Jain, Ashay ; Thakur, Deepika ; Ghoshal, Gargi ; Katare, O.P. ; Singh, Bhupinder ; Shivhare, U.S.</creatorcontrib><description>•Microencapsulation of lycopene was carried out by coacervation method.•Casein and Gum tragacanth was used as coating material.•The microencapsules fabricated at 1:2 of Gt:Cas were also revealed the highest loading capacity and maximum coacervates yield.•Cumulative lycopene release was estimated 86.34±2.69% from microencapsulated formulations at the end of 24th h.•The stability of lycopene in that formulation in term of % residual content were studied for three months. The current work entails a novel strategy of formulating the microparticles of lycopene solely using rational blends of biopolymers without using equipment-intensive techniques. The study is intended to enhance oral bioavailability of lycopene by controlling its release from micro-formulation and facilitating its absorption though lymphatic pathways. Considering the minimum particle size, maximum entrapment efficiency and loading capacity, the amounts of casein (i.e., protein) and gum tragacanth (i.e., polysaccharide) were selected as the critical factors for formulation of microparticles. Complex formation and electrostatic interaction was confirmed by Fourier transform infra red (FTIR) spectra. Size and surface properties of microparticles were studied using scanning electron microscopy (SEM). The optimized formulation (mean particle size: ∼130μm; % entrapment efficiency: ∼67% and loading capacity: ∼71%) designated noticeable improvement in lycopene release profile (over 80% in 24h). Increment in the values of Cmax (2.22-fold) and AUC (1.97-fold) further indicated noteworthy augmentation in the rate and extent of bioavailability by the microparticles formulation compared to plain lycopene. The resulting formulation was found to be quite stable all through two months of study episode. The resultant microparticles formulation was evaluated for antioxidant activity and tested for their effectiveness in self life enhancement of vegetable oil by calculating peroxide value under temperature and storage condition. Encapsulation strongly increased the stability of micronutrients. The current investigations, therefore, report the successful development of biopolymeric microparticles with improved bioavailability potential of lycopene.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2016.08.071</identifier><identifier>PMID: 27575434</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antioxidant activity ; Bioavailability ; Carotenoids - chemistry ; Carotenoids - pharmacokinetics ; Carotenoids - pharmacology ; Caseins - chemistry ; Caseins - pharmacokinetics ; Caseins - pharmacology ; Coacervation ; Drug Carriers - chemistry ; Drug Carriers - pharmacokinetics ; Drug Carriers - pharmacology ; Lycopene ; Male ; Microparticles ; Oral Mucosal Absorption ; Polysaccharides - chemistry ; Polysaccharides - pharmacokinetics ; Polysaccharides - pharmacology ; Rats ; Rats, Wistar ; Static Electricity</subject><ispartof>International journal of biological macromolecules, 2016-12, Vol.93 (Pt A), p.746-756</ispartof><rights>2016</rights><rights>Copyright © 2016. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-6e17bf67f2b8c59dea754a827f26ef03fefcbc7baf542972029ace484f3e5b523</citedby><cites>FETCH-LOGICAL-c368t-6e17bf67f2b8c59dea754a827f26ef03fefcbc7baf542972029ace484f3e5b523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0141813016307887$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27575434$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jain, Ashay</creatorcontrib><creatorcontrib>Thakur, Deepika</creatorcontrib><creatorcontrib>Ghoshal, Gargi</creatorcontrib><creatorcontrib>Katare, O.P.</creatorcontrib><creatorcontrib>Singh, Bhupinder</creatorcontrib><creatorcontrib>Shivhare, U.S.</creatorcontrib><title>Formation and functional attributes of electrostatic complexes involving casein and anionic polysaccharides: An approach to enhance oral absorption of lycopene in rats in vivo</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>•Microencapsulation of lycopene was carried out by coacervation method.•Casein and Gum tragacanth was used as coating material.•The microencapsules fabricated at 1:2 of Gt:Cas were also revealed the highest loading capacity and maximum coacervates yield.•Cumulative lycopene release was estimated 86.34±2.69% from microencapsulated formulations at the end of 24th h.•The stability of lycopene in that formulation in term of % residual content were studied for three months. The current work entails a novel strategy of formulating the microparticles of lycopene solely using rational blends of biopolymers without using equipment-intensive techniques. The study is intended to enhance oral bioavailability of lycopene by controlling its release from micro-formulation and facilitating its absorption though lymphatic pathways. Considering the minimum particle size, maximum entrapment efficiency and loading capacity, the amounts of casein (i.e., protein) and gum tragacanth (i.e., polysaccharide) were selected as the critical factors for formulation of microparticles. Complex formation and electrostatic interaction was confirmed by Fourier transform infra red (FTIR) spectra. Size and surface properties of microparticles were studied using scanning electron microscopy (SEM). The optimized formulation (mean particle size: ∼130μm; % entrapment efficiency: ∼67% and loading capacity: ∼71%) designated noticeable improvement in lycopene release profile (over 80% in 24h). Increment in the values of Cmax (2.22-fold) and AUC (1.97-fold) further indicated noteworthy augmentation in the rate and extent of bioavailability by the microparticles formulation compared to plain lycopene. The resulting formulation was found to be quite stable all through two months of study episode. The resultant microparticles formulation was evaluated for antioxidant activity and tested for their effectiveness in self life enhancement of vegetable oil by calculating peroxide value under temperature and storage condition. Encapsulation strongly increased the stability of micronutrients. The current investigations, therefore, report the successful development of biopolymeric microparticles with improved bioavailability potential of lycopene.</description><subject>Animals</subject><subject>Antioxidant activity</subject><subject>Bioavailability</subject><subject>Carotenoids - chemistry</subject><subject>Carotenoids - pharmacokinetics</subject><subject>Carotenoids - pharmacology</subject><subject>Caseins - chemistry</subject><subject>Caseins - pharmacokinetics</subject><subject>Caseins - pharmacology</subject><subject>Coacervation</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Carriers - pharmacokinetics</subject><subject>Drug Carriers - pharmacology</subject><subject>Lycopene</subject><subject>Male</subject><subject>Microparticles</subject><subject>Oral Mucosal Absorption</subject><subject>Polysaccharides - chemistry</subject><subject>Polysaccharides - pharmacokinetics</subject><subject>Polysaccharides - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Static Electricity</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1v1DAQtRAVXQp_ofKRS4Id58PLiaqiLVIlLuVsOc6Y9Sqxg-1E7K_iLzJhW66cRjPz5r2ZeYRcc1ZyxtuPx9IdexcmbcoK85LJknX8Fdlx2e0Lxph4TXaM17yQXLBL8jalI1bbhss35LLqmq6pRb0jv-9CnHR2wVPtB2oXb7ZEj1TnHF2_ZEg0WAojmBxDyog11IRpHuEXtpxfw7g6_4MancCdWbRHCoTNYTwlbcxBRzdA-kRvsD_PMWhzoDlQ8AftDdAQN70-hTj_3QT1xpMJM3hAARp13oTo6tbwjlxYPSZ4_xyvyPe7L0-3D8Xjt_uvtzePhRGtzEULvOtt29mql6bZD6DxXi0rLLRgmbBgTW-6XtumrvZdxaq9NlDL2gpo-qYSV-TDmRe3_blAympyycA4ag9hSYpL0YimY61AaHuGGvxPimDVHN2k40lxpjaz1FG9mKU2sxSTCs3CwetnjaWfYPg39uIOAj6fAYCXrg6iSsYBfmxwEe1QQ3D_0_gDkyiu7A</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Jain, Ashay</creator><creator>Thakur, Deepika</creator><creator>Ghoshal, Gargi</creator><creator>Katare, O.P.</creator><creator>Singh, Bhupinder</creator><creator>Shivhare, U.S.</creator><general>Elsevier B.V</general><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>7X8</scope></search><sort><creationdate>201612</creationdate><title>Formation and functional attributes of electrostatic complexes involving casein and anionic polysaccharides: An approach to enhance oral absorption of lycopene in rats in vivo</title><author>Jain, Ashay ; Thakur, Deepika ; Ghoshal, Gargi ; Katare, O.P. ; Singh, Bhupinder ; Shivhare, U.S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-6e17bf67f2b8c59dea754a827f26ef03fefcbc7baf542972029ace484f3e5b523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antioxidant activity</topic><topic>Bioavailability</topic><topic>Carotenoids - chemistry</topic><topic>Carotenoids - pharmacokinetics</topic><topic>Carotenoids - pharmacology</topic><topic>Caseins - chemistry</topic><topic>Caseins - pharmacokinetics</topic><topic>Caseins - pharmacology</topic><topic>Coacervation</topic><topic>Drug Carriers - chemistry</topic><topic>Drug Carriers - pharmacokinetics</topic><topic>Drug Carriers - pharmacology</topic><topic>Lycopene</topic><topic>Male</topic><topic>Microparticles</topic><topic>Oral Mucosal Absorption</topic><topic>Polysaccharides - chemistry</topic><topic>Polysaccharides - pharmacokinetics</topic><topic>Polysaccharides - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Static Electricity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jain, Ashay</creatorcontrib><creatorcontrib>Thakur, Deepika</creatorcontrib><creatorcontrib>Ghoshal, Gargi</creatorcontrib><creatorcontrib>Katare, O.P.</creatorcontrib><creatorcontrib>Singh, Bhupinder</creatorcontrib><creatorcontrib>Shivhare, U.S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jain, Ashay</au><au>Thakur, Deepika</au><au>Ghoshal, Gargi</au><au>Katare, O.P.</au><au>Singh, Bhupinder</au><au>Shivhare, U.S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formation and functional attributes of electrostatic complexes involving casein and anionic polysaccharides: An approach to enhance oral absorption of lycopene in rats in vivo</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2016-12</date><risdate>2016</risdate><volume>93</volume><issue>Pt A</issue><spage>746</spage><epage>756</epage><pages>746-756</pages><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>•Microencapsulation of lycopene was carried out by coacervation method.•Casein and Gum tragacanth was used as coating material.•The microencapsules fabricated at 1:2 of Gt:Cas were also revealed the highest loading capacity and maximum coacervates yield.•Cumulative lycopene release was estimated 86.34±2.69% from microencapsulated formulations at the end of 24th h.•The stability of lycopene in that formulation in term of % residual content were studied for three months. The current work entails a novel strategy of formulating the microparticles of lycopene solely using rational blends of biopolymers without using equipment-intensive techniques. The study is intended to enhance oral bioavailability of lycopene by controlling its release from micro-formulation and facilitating its absorption though lymphatic pathways. Considering the minimum particle size, maximum entrapment efficiency and loading capacity, the amounts of casein (i.e., protein) and gum tragacanth (i.e., polysaccharide) were selected as the critical factors for formulation of microparticles. Complex formation and electrostatic interaction was confirmed by Fourier transform infra red (FTIR) spectra. Size and surface properties of microparticles were studied using scanning electron microscopy (SEM). The optimized formulation (mean particle size: ∼130μm; % entrapment efficiency: ∼67% and loading capacity: ∼71%) designated noticeable improvement in lycopene release profile (over 80% in 24h). Increment in the values of Cmax (2.22-fold) and AUC (1.97-fold) further indicated noteworthy augmentation in the rate and extent of bioavailability by the microparticles formulation compared to plain lycopene. The resulting formulation was found to be quite stable all through two months of study episode. The resultant microparticles formulation was evaluated for antioxidant activity and tested for their effectiveness in self life enhancement of vegetable oil by calculating peroxide value under temperature and storage condition. Encapsulation strongly increased the stability of micronutrients. The current investigations, therefore, report the successful development of biopolymeric microparticles with improved bioavailability potential of lycopene.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27575434</pmid><doi>10.1016/j.ijbiomac.2016.08.071</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0141-8130
ispartof International journal of biological macromolecules, 2016-12, Vol.93 (Pt A), p.746-756
issn 0141-8130
1879-0003
language eng
recordid cdi_proquest_miscellaneous_1835357063
source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Antioxidant activity
Bioavailability
Carotenoids - chemistry
Carotenoids - pharmacokinetics
Carotenoids - pharmacology
Caseins - chemistry
Caseins - pharmacokinetics
Caseins - pharmacology
Coacervation
Drug Carriers - chemistry
Drug Carriers - pharmacokinetics
Drug Carriers - pharmacology
Lycopene
Male
Microparticles
Oral Mucosal Absorption
Polysaccharides - chemistry
Polysaccharides - pharmacokinetics
Polysaccharides - pharmacology
Rats
Rats, Wistar
Static Electricity
title Formation and functional attributes of electrostatic complexes involving casein and anionic polysaccharides: An approach to enhance oral absorption of lycopene in rats in vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T18%3A15%3A52IST&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=Formation%20and%20functional%20attributes%20of%20electrostatic%20complexes%20involving%20casein%20and%20anionic%20polysaccharides:%20An%20approach%20to%20enhance%20oral%20absorption%20of%20lycopene%20in%20rats%20in%20vivo&rft.jtitle=International%20journal%20of%20biological%20macromolecules&rft.au=Jain,%20Ashay&rft.date=2016-12&rft.volume=93&rft.issue=Pt%20A&rft.spage=746&rft.epage=756&rft.pages=746-756&rft.issn=0141-8130&rft.eissn=1879-0003&rft_id=info:doi/10.1016/j.ijbiomac.2016.08.071&rft_dat=%3Cproquest_cross%3E1835357063%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=1835357063&rft_id=info:pmid/27575434&rft_els_id=S0141813016307887&rfr_iscdi=true