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Inspiring biomimetic system based on red blood cell membrane vesicles for effective curcumin loading and release
[Display omitted] The aim of this study is to introduce an inspiring biomimetic system based on the red blood cell membrane (RBCM) vesicles for improved encapsulation efficiency and release of curcumin (Cur). Here, the role of the sonication time (0.5, 1.5, 3 and 5 min) on the properties of RBCM-CUR...
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Published in: | International journal of pharmaceutics 2022-02, Vol.613, p.121419-121419, Article 121419 |
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container_title | International journal of pharmaceutics |
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creator | Safarpour, F. Kharaziha, M. Emadi, R. |
description | [Display omitted]
The aim of this study is to introduce an inspiring biomimetic system based on the red blood cell membrane (RBCM) vesicles for improved encapsulation efficiency and release of curcumin (Cur). Here, the role of the sonication time (0.5, 1.5, 3 and 5 min) on the properties of RBCM-CUR vesicles is investigated. It is determined that the hydrodynamic vesicle size, zeta potential, and release behavior are tunable by changing the sonication time. Noticeably, the average size of vesicles decreased from 163.0 ± 21 nm to 116.3 ± 16 nm by increasing the sonication time from 0.5 to 5 min. Moreover, the drug release value, after 24 h incubation, enhances from 57 to 99% with the expansion of sonication from 0.5 to 5 min. Additionally, the entrapment efficiency of Cur as a model drug is high in whole sonication time, owing to the amphiphilic nature of RBCM. Finally, the RBCM-CUR vesicles are not only cytocompatible, but also could support the attachment and proliferation of fibroblast cells in vitro. The RBCM based system for delivery of Cur could be a promising system for the wound healing applications. |
doi_str_mv | 10.1016/j.ijpharm.2021.121419 |
format | article |
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The aim of this study is to introduce an inspiring biomimetic system based on the red blood cell membrane (RBCM) vesicles for improved encapsulation efficiency and release of curcumin (Cur). Here, the role of the sonication time (0.5, 1.5, 3 and 5 min) on the properties of RBCM-CUR vesicles is investigated. It is determined that the hydrodynamic vesicle size, zeta potential, and release behavior are tunable by changing the sonication time. Noticeably, the average size of vesicles decreased from 163.0 ± 21 nm to 116.3 ± 16 nm by increasing the sonication time from 0.5 to 5 min. Moreover, the drug release value, after 24 h incubation, enhances from 57 to 99% with the expansion of sonication from 0.5 to 5 min. Additionally, the entrapment efficiency of Cur as a model drug is high in whole sonication time, owing to the amphiphilic nature of RBCM. Finally, the RBCM-CUR vesicles are not only cytocompatible, but also could support the attachment and proliferation of fibroblast cells in vitro. The RBCM based system for delivery of Cur could be a promising system for the wound healing applications.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2021.121419</identifier><identifier>PMID: 34954002</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Biocompatibility ; Biomimetics ; Curcumin ; Drug Carriers ; Drug delivery ; Erythrocytes ; Inspiring biomimetic system ; Particle Size ; Red blood cell membrane ; Vesicles</subject><ispartof>International journal of pharmaceutics, 2022-02, Vol.613, p.121419-121419, Article 121419</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-a33d6479c99401667c4317edac4d8fca5c5dd8d55a23d82184e0b27adb2a64c23</citedby><cites>FETCH-LOGICAL-c365t-a33d6479c99401667c4317edac4d8fca5c5dd8d55a23d82184e0b27adb2a64c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34954002$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Safarpour, F.</creatorcontrib><creatorcontrib>Kharaziha, M.</creatorcontrib><creatorcontrib>Emadi, R.</creatorcontrib><title>Inspiring biomimetic system based on red blood cell membrane vesicles for effective curcumin loading and release</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted]
The aim of this study is to introduce an inspiring biomimetic system based on the red blood cell membrane (RBCM) vesicles for improved encapsulation efficiency and release of curcumin (Cur). Here, the role of the sonication time (0.5, 1.5, 3 and 5 min) on the properties of RBCM-CUR vesicles is investigated. It is determined that the hydrodynamic vesicle size, zeta potential, and release behavior are tunable by changing the sonication time. Noticeably, the average size of vesicles decreased from 163.0 ± 21 nm to 116.3 ± 16 nm by increasing the sonication time from 0.5 to 5 min. Moreover, the drug release value, after 24 h incubation, enhances from 57 to 99% with the expansion of sonication from 0.5 to 5 min. Additionally, the entrapment efficiency of Cur as a model drug is high in whole sonication time, owing to the amphiphilic nature of RBCM. Finally, the RBCM-CUR vesicles are not only cytocompatible, but also could support the attachment and proliferation of fibroblast cells in vitro. The RBCM based system for delivery of Cur could be a promising system for the wound healing applications.</description><subject>Biocompatibility</subject><subject>Biomimetics</subject><subject>Curcumin</subject><subject>Drug Carriers</subject><subject>Drug delivery</subject><subject>Erythrocytes</subject><subject>Inspiring biomimetic system</subject><subject>Particle Size</subject><subject>Red blood cell membrane</subject><subject>Vesicles</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkMtq3DAUhkVoSKZJHqFFy2481V32qpSQGwS6adZClo5TDZblSvZA3j4aZtptVmfzn__yIfSFki0lVH3fbcNu_mNz3DLC6JYyKmh3hja01bzhQqtPaEO4bhtJNb9En0vZEUIUo_wCXXLRSUEI26D5aSpzyGF6xX1IMURYgsPlrSwQcW8LeJwmnOvpx5Q8djCOOELss50A76EEN0LBQ8oYhgHcEvaA3ZrdGsOEx2T9wdpOvnqMUP2u0flgxwI3p3uFXu7vft8-Ns-_Hp5ufz43jiu5NJZzr4TuXNeJOldpJzjV4K0Tvh2clU5633opLeO-ZbQVQHqmre-ZVcIxfoW-HX3nnP6uUBYTQzm0r73TWgxTVGjZKiqrVB6lLqdSMgxmziHa_GYoMQfYZmdOsM0BtjnCrn9fTxFrH8H___pHtwp-HAVQh-4DZFNcgMmBD7miMj6FDyLeATvMlIk</recordid><startdate>20220205</startdate><enddate>20220205</enddate><creator>Safarpour, F.</creator><creator>Kharaziha, M.</creator><creator>Emadi, R.</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>20220205</creationdate><title>Inspiring biomimetic system based on red blood cell membrane vesicles for effective curcumin loading and release</title><author>Safarpour, F. ; Kharaziha, M. ; Emadi, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-a33d6479c99401667c4317edac4d8fca5c5dd8d55a23d82184e0b27adb2a64c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biocompatibility</topic><topic>Biomimetics</topic><topic>Curcumin</topic><topic>Drug Carriers</topic><topic>Drug delivery</topic><topic>Erythrocytes</topic><topic>Inspiring biomimetic system</topic><topic>Particle Size</topic><topic>Red blood cell membrane</topic><topic>Vesicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Safarpour, F.</creatorcontrib><creatorcontrib>Kharaziha, M.</creatorcontrib><creatorcontrib>Emadi, R.</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 pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Safarpour, F.</au><au>Kharaziha, M.</au><au>Emadi, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inspiring biomimetic system based on red blood cell membrane vesicles for effective curcumin loading and release</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2022-02-05</date><risdate>2022</risdate><volume>613</volume><spage>121419</spage><epage>121419</epage><pages>121419-121419</pages><artnum>121419</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
The aim of this study is to introduce an inspiring biomimetic system based on the red blood cell membrane (RBCM) vesicles for improved encapsulation efficiency and release of curcumin (Cur). Here, the role of the sonication time (0.5, 1.5, 3 and 5 min) on the properties of RBCM-CUR vesicles is investigated. It is determined that the hydrodynamic vesicle size, zeta potential, and release behavior are tunable by changing the sonication time. Noticeably, the average size of vesicles decreased from 163.0 ± 21 nm to 116.3 ± 16 nm by increasing the sonication time from 0.5 to 5 min. Moreover, the drug release value, after 24 h incubation, enhances from 57 to 99% with the expansion of sonication from 0.5 to 5 min. Additionally, the entrapment efficiency of Cur as a model drug is high in whole sonication time, owing to the amphiphilic nature of RBCM. Finally, the RBCM-CUR vesicles are not only cytocompatible, but also could support the attachment and proliferation of fibroblast cells in vitro. The RBCM based system for delivery of Cur could be a promising system for the wound healing applications.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34954002</pmid><doi>10.1016/j.ijpharm.2021.121419</doi><tpages>1</tpages></addata></record> |
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subjects | Biocompatibility Biomimetics Curcumin Drug Carriers Drug delivery Erythrocytes Inspiring biomimetic system Particle Size Red blood cell membrane Vesicles |
title | Inspiring biomimetic system based on red blood cell membrane vesicles for effective curcumin loading and release |
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