Synthesis and characterization of PEGylated bolaamphiphiles with enhanced retention in liposomes
[Display omitted] Long-circulating liposomes are typically prepared with poly(ethylene glycol)- (PEG-) modified lipids, where the lipid portion is inserted in the lipid bilayers as an anchor and the hydrophilic PEG coats the surface to prevent liposome aggregation and rapid clearance in vivo. Howeve...
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Veröffentlicht in: | Journal of colloid and interface science 2016-11, Vol.482, p.19-26 |
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Long-circulating liposomes are typically prepared with poly(ethylene glycol)- (PEG-) modified lipids, where the lipid portion is inserted in the lipid bilayers as an anchor and the hydrophilic PEG coats the surface to prevent liposome aggregation and rapid clearance in vivo. However, these steric protection effects are compromised upon systemic administration due to low retention of PEGylated lipids within liposome membranes upon dilution. Hence, a series of PEGylated bolaamphiphiles (PEG-bolas) were for the first time developed to increase retention in the lipid bilayer, presumably leading to enhanced integrity of the PEG protective layer upon dilution. We hypothesized that PEG-bolas with a sufficiently long hydrophobic domain and rigid central group could predominantly adopt a membrane-spanning configuration, taking full advantage of steric protection offered by PEG and enhanced retention in liposomes enabled by the bola geometry. In this paper, liposomes stabilized by PEG-bolas comprised of a biphenyl core and twelve-carbon alkyl chain not only exhibited similar storage and biological stability compared to conventional PEGylated lipid stabilized liposomes, but also significantly improved retention upon dilution. Our findings facilitate new designs of liposome-stabilizing agents and can be applied to improve the delivery efficiency of liposomal delivery vehicles in vivo. |
doi_str_mv | 10.1016/j.jcis.2016.07.013 |
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Long-circulating liposomes are typically prepared with poly(ethylene glycol)- (PEG-) modified lipids, where the lipid portion is inserted in the lipid bilayers as an anchor and the hydrophilic PEG coats the surface to prevent liposome aggregation and rapid clearance in vivo. However, these steric protection effects are compromised upon systemic administration due to low retention of PEGylated lipids within liposome membranes upon dilution. Hence, a series of PEGylated bolaamphiphiles (PEG-bolas) were for the first time developed to increase retention in the lipid bilayer, presumably leading to enhanced integrity of the PEG protective layer upon dilution. We hypothesized that PEG-bolas with a sufficiently long hydrophobic domain and rigid central group could predominantly adopt a membrane-spanning configuration, taking full advantage of steric protection offered by PEG and enhanced retention in liposomes enabled by the bola geometry. In this paper, liposomes stabilized by PEG-bolas comprised of a biphenyl core and twelve-carbon alkyl chain not only exhibited similar storage and biological stability compared to conventional PEGylated lipid stabilized liposomes, but also significantly improved retention upon dilution. Our findings facilitate new designs of liposome-stabilizing agents and can be applied to improve the delivery efficiency of liposomal delivery vehicles in vivo.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2016.07.013</identifier><identifier>PMID: 27485501</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>1,2-Dipalmitoylphosphatidylcholine - chemistry ; Air - analysis ; Bolaamphiphile ; Cholesterol - chemistry ; Drug delivery ; Furans - chemical synthesis ; Furans - chemistry ; Humans ; Hydrophobic and Hydrophilic Interactions ; Kinetics ; Lipid Bilayers - chemistry ; Lipid Bilayers - pharmacology ; Liposomes ; Liposomes - chemistry ; Liposomes - pharmacology ; Long-circulation ; Macrophages - cytology ; Macrophages - drug effects ; Particle Size ; PEGylated lipids ; Phagocytosis - drug effects ; Polyethylene Glycols - chemistry ; Pyridones - chemical synthesis ; Pyridones - chemistry ; Steric stabilization ; Surface Properties ; Water - chemistry</subject><ispartof>Journal of colloid and interface science, 2016-11, Vol.482, p.19-26</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-c894c031c09995d4adc1a94f8a13e2bc4bcbdea831a74328f49fd7d99ad9e413</citedby><cites>FETCH-LOGICAL-c393t-c894c031c09995d4adc1a94f8a13e2bc4bcbdea831a74328f49fd7d99ad9e413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021979716304726$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27485501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Yingyue</creatorcontrib><creatorcontrib>Mintzer, Evan</creatorcontrib><creatorcontrib>Uhrich, Kathryn E.</creatorcontrib><title>Synthesis and characterization of PEGylated bolaamphiphiles with enhanced retention in liposomes</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>[Display omitted]
Long-circulating liposomes are typically prepared with poly(ethylene glycol)- (PEG-) modified lipids, where the lipid portion is inserted in the lipid bilayers as an anchor and the hydrophilic PEG coats the surface to prevent liposome aggregation and rapid clearance in vivo. However, these steric protection effects are compromised upon systemic administration due to low retention of PEGylated lipids within liposome membranes upon dilution. Hence, a series of PEGylated bolaamphiphiles (PEG-bolas) were for the first time developed to increase retention in the lipid bilayer, presumably leading to enhanced integrity of the PEG protective layer upon dilution. We hypothesized that PEG-bolas with a sufficiently long hydrophobic domain and rigid central group could predominantly adopt a membrane-spanning configuration, taking full advantage of steric protection offered by PEG and enhanced retention in liposomes enabled by the bola geometry. In this paper, liposomes stabilized by PEG-bolas comprised of a biphenyl core and twelve-carbon alkyl chain not only exhibited similar storage and biological stability compared to conventional PEGylated lipid stabilized liposomes, but also significantly improved retention upon dilution. Our findings facilitate new designs of liposome-stabilizing agents and can be applied to improve the delivery efficiency of liposomal delivery vehicles in vivo.</description><subject>1,2-Dipalmitoylphosphatidylcholine - chemistry</subject><subject>Air - analysis</subject><subject>Bolaamphiphile</subject><subject>Cholesterol - chemistry</subject><subject>Drug delivery</subject><subject>Furans - chemical synthesis</subject><subject>Furans - chemistry</subject><subject>Humans</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Kinetics</subject><subject>Lipid Bilayers - chemistry</subject><subject>Lipid Bilayers - pharmacology</subject><subject>Liposomes</subject><subject>Liposomes - chemistry</subject><subject>Liposomes - pharmacology</subject><subject>Long-circulation</subject><subject>Macrophages - cytology</subject><subject>Macrophages - drug effects</subject><subject>Particle Size</subject><subject>PEGylated lipids</subject><subject>Phagocytosis - drug effects</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Pyridones - chemical synthesis</subject><subject>Pyridones - chemistry</subject><subject>Steric stabilization</subject><subject>Surface Properties</subject><subject>Water - chemistry</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMoun78AQ_So5fWTNPaBryI-AWCgt7jNJnSLG2zJlll_fV2XfUoDGQgz_vCPIwdA8-Aw_nZPJtrG7J82jNeZRzEFpsBl2VaARfbbMZ5DqmsZLXH9kOYcw5QlnKX7eVVUZclhxl7fV6NsaNgQ4KjSXSHHnUkbz8xWjcmrk2erm9XPUYySeN6xGHR2Wl6CsmHjV1CY4ejnn49RRq_Q3ZMertwwQ0UDtlOi32go5_3gL3cXL9c3aUPj7f3V5cPqRZSxFTXstBcgOZSytIUaDSgLNoaQVDe6KLRjSGsBWBViLxuC9maykiJRlIB4oCdbmoX3r0tKUQ12KCp73EktwwKaijPa4BvNN-g2rsQPLVq4e2AfqWAq7VYNVdrsWotVvFKTWKn0MlP_7IZyPxFfk1OwMUGoOnId0teBW1pLcZ60lEZZ__r_wKmk4vr</recordid><startdate>20161115</startdate><enddate>20161115</enddate><creator>Zhang, Yingyue</creator><creator>Mintzer, Evan</creator><creator>Uhrich, Kathryn E.</creator><general>Elsevier Inc</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>20161115</creationdate><title>Synthesis and characterization of PEGylated bolaamphiphiles with enhanced retention in liposomes</title><author>Zhang, Yingyue ; Mintzer, Evan ; Uhrich, Kathryn E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-c894c031c09995d4adc1a94f8a13e2bc4bcbdea831a74328f49fd7d99ad9e413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>1,2-Dipalmitoylphosphatidylcholine - chemistry</topic><topic>Air - analysis</topic><topic>Bolaamphiphile</topic><topic>Cholesterol - chemistry</topic><topic>Drug delivery</topic><topic>Furans - chemical synthesis</topic><topic>Furans - chemistry</topic><topic>Humans</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Kinetics</topic><topic>Lipid Bilayers - chemistry</topic><topic>Lipid Bilayers - pharmacology</topic><topic>Liposomes</topic><topic>Liposomes - chemistry</topic><topic>Liposomes - pharmacology</topic><topic>Long-circulation</topic><topic>Macrophages - cytology</topic><topic>Macrophages - drug effects</topic><topic>Particle Size</topic><topic>PEGylated lipids</topic><topic>Phagocytosis - drug effects</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Pyridones - chemical synthesis</topic><topic>Pyridones - chemistry</topic><topic>Steric stabilization</topic><topic>Surface Properties</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yingyue</creatorcontrib><creatorcontrib>Mintzer, Evan</creatorcontrib><creatorcontrib>Uhrich, Kathryn E.</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>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Yingyue</au><au>Mintzer, Evan</au><au>Uhrich, Kathryn E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and characterization of PEGylated bolaamphiphiles with enhanced retention in liposomes</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2016-11-15</date><risdate>2016</risdate><volume>482</volume><spage>19</spage><epage>26</epage><pages>19-26</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><abstract>[Display omitted]
Long-circulating liposomes are typically prepared with poly(ethylene glycol)- (PEG-) modified lipids, where the lipid portion is inserted in the lipid bilayers as an anchor and the hydrophilic PEG coats the surface to prevent liposome aggregation and rapid clearance in vivo. However, these steric protection effects are compromised upon systemic administration due to low retention of PEGylated lipids within liposome membranes upon dilution. Hence, a series of PEGylated bolaamphiphiles (PEG-bolas) were for the first time developed to increase retention in the lipid bilayer, presumably leading to enhanced integrity of the PEG protective layer upon dilution. We hypothesized that PEG-bolas with a sufficiently long hydrophobic domain and rigid central group could predominantly adopt a membrane-spanning configuration, taking full advantage of steric protection offered by PEG and enhanced retention in liposomes enabled by the bola geometry. In this paper, liposomes stabilized by PEG-bolas comprised of a biphenyl core and twelve-carbon alkyl chain not only exhibited similar storage and biological stability compared to conventional PEGylated lipid stabilized liposomes, but also significantly improved retention upon dilution. Our findings facilitate new designs of liposome-stabilizing agents and can be applied to improve the delivery efficiency of liposomal delivery vehicles in vivo.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27485501</pmid><doi>10.1016/j.jcis.2016.07.013</doi><tpages>8</tpages></addata></record> |
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subjects | 1,2-Dipalmitoylphosphatidylcholine - chemistry Air - analysis Bolaamphiphile Cholesterol - chemistry Drug delivery Furans - chemical synthesis Furans - chemistry Humans Hydrophobic and Hydrophilic Interactions Kinetics Lipid Bilayers - chemistry Lipid Bilayers - pharmacology Liposomes Liposomes - chemistry Liposomes - pharmacology Long-circulation Macrophages - cytology Macrophages - drug effects Particle Size PEGylated lipids Phagocytosis - drug effects Polyethylene Glycols - chemistry Pyridones - chemical synthesis Pyridones - chemistry Steric stabilization Surface Properties Water - chemistry |
title | Synthesis and characterization of PEGylated bolaamphiphiles with enhanced retention in liposomes |
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