The influence of dipalmitoyl phosphatidylserine on phase behaviour of and cellular response to lyotropic liquid crystalline dispersions
Abstract Lyotropic liquid crystalline nanoparticles (cubosomes) have the potential to act as amphiphilic scaffolds for the presentation of lipids and subsequent application in, for example, bioseparations and therapeutic delivery. In this work we have formulated lyotropic liquid crystalline systems...
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Veröffentlicht in: | Biomaterials 2010-12, Vol.31 (36), p.9473-9481 |
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description | Abstract Lyotropic liquid crystalline nanoparticles (cubosomes) have the potential to act as amphiphilic scaffolds for the presentation of lipids and subsequent application in, for example, bioseparations and therapeutic delivery. In this work we have formulated lyotropic liquid crystalline systems based on the synthetic amphiphile 1,2,3-trihydroxy-3,7,11,15-tetramethylhexadecane (phytantriol) and containing the lipid dipalmitoyl phosphatidylserine (DPPS). We have prepared a range of DPPS-containing phytantriol cubosome formulations and characterized them using Small Angle X-ray Scattering and Cryo-transmission electron microscopy. These techniques show that increased DPPS content induces marked changes in lyotropic liquid crystalline phase behaviour, characterized by changes in crystallographic dimensions and increases in vesicle content. Furthermore, in vitro cell culture studies indicate that these changes correlate with lipid/surfactant cellular uptake and cytotoxicity. A model cell membrane based on a surface supported phospholipid bilayer was used to gain insights into cubosome–bilayer interactions using Quartz Crystal Microgravimetry. The data show that mass uptake at the supported bilayer increased with DPPS content. We propose that the cytotoxicity of the DPPS-containing dispersions results from changes in lipid/surfactant phase behaviour and the preferential attachment and fusion of vesicles at the cell membrane. |
doi_str_mv | 10.1016/j.biomaterials.2010.08.030 |
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In this work we have formulated lyotropic liquid crystalline systems based on the synthetic amphiphile 1,2,3-trihydroxy-3,7,11,15-tetramethylhexadecane (phytantriol) and containing the lipid dipalmitoyl phosphatidylserine (DPPS). We have prepared a range of DPPS-containing phytantriol cubosome formulations and characterized them using Small Angle X-ray Scattering and Cryo-transmission electron microscopy. These techniques show that increased DPPS content induces marked changes in lyotropic liquid crystalline phase behaviour, characterized by changes in crystallographic dimensions and increases in vesicle content. Furthermore, in vitro cell culture studies indicate that these changes correlate with lipid/surfactant cellular uptake and cytotoxicity. A model cell membrane based on a surface supported phospholipid bilayer was used to gain insights into cubosome–bilayer interactions using Quartz Crystal Microgravimetry. The data show that mass uptake at the supported bilayer increased with DPPS content. We propose that the cytotoxicity of the DPPS-containing dispersions results from changes in lipid/surfactant phase behaviour and the preferential attachment and fusion of vesicles at the cell membrane.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2010.08.030</identifier><identifier>PMID: 20880581</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Advanced Basic Science ; Animals ; Cell Death - drug effects ; Cell Line ; Cell Survival - drug effects ; Confocal microscopy ; Cubosomes ; Cytotoxicity ; Dentistry ; Fatty Alcohols - pharmacology ; Fibroblasts - cytology ; Fibroblasts - drug effects ; Fibroblasts - metabolism ; Liquid Crystals - chemistry ; Mice ; Microscopy, Confocal ; Nanoparticles - ultrastructure ; Particle Size ; Phase behaviour ; Phase Transition - drug effects ; Phosphatidylserines - pharmacology ; Phytantriol ; Quartz Crystal Microbalance Techniques ; Scattering, Small Angle ; Small angle X-ray scattering ; Static Electricity ; Surface-Active Agents - pharmacology ; Synchrotrons ; Unilamellar Liposomes - chemistry ; X-Ray Diffraction</subject><ispartof>Biomaterials, 2010-12, Vol.31 (36), p.9473-9481</ispartof><rights>2010</rights><rights>Crown Copyright © 2010. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-9b6a8afdbded9dddc73c9920215c4ebb3c3f01b12fe952e5cab46d3f26381d663</citedby><cites>FETCH-LOGICAL-c466t-9b6a8afdbded9dddc73c9920215c4ebb3c3f01b12fe952e5cab46d3f26381d663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biomaterials.2010.08.030$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20880581$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shen, Hsin-Hui</creatorcontrib><creatorcontrib>Crowston, Jonathan G</creatorcontrib><creatorcontrib>Huber, Florian</creatorcontrib><creatorcontrib>Saubern, Simon</creatorcontrib><creatorcontrib>McLean, Keith M</creatorcontrib><creatorcontrib>Hartley, Patrick G</creatorcontrib><title>The influence of dipalmitoyl phosphatidylserine on phase behaviour of and cellular response to lyotropic liquid crystalline dispersions</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>Abstract Lyotropic liquid crystalline nanoparticles (cubosomes) have the potential to act as amphiphilic scaffolds for the presentation of lipids and subsequent application in, for example, bioseparations and therapeutic delivery. In this work we have formulated lyotropic liquid crystalline systems based on the synthetic amphiphile 1,2,3-trihydroxy-3,7,11,15-tetramethylhexadecane (phytantriol) and containing the lipid dipalmitoyl phosphatidylserine (DPPS). We have prepared a range of DPPS-containing phytantriol cubosome formulations and characterized them using Small Angle X-ray Scattering and Cryo-transmission electron microscopy. These techniques show that increased DPPS content induces marked changes in lyotropic liquid crystalline phase behaviour, characterized by changes in crystallographic dimensions and increases in vesicle content. Furthermore, in vitro cell culture studies indicate that these changes correlate with lipid/surfactant cellular uptake and cytotoxicity. A model cell membrane based on a surface supported phospholipid bilayer was used to gain insights into cubosome–bilayer interactions using Quartz Crystal Microgravimetry. The data show that mass uptake at the supported bilayer increased with DPPS content. We propose that the cytotoxicity of the DPPS-containing dispersions results from changes in lipid/surfactant phase behaviour and the preferential attachment and fusion of vesicles at the cell membrane.</description><subject>Advanced Basic Science</subject><subject>Animals</subject><subject>Cell Death - drug effects</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Confocal microscopy</subject><subject>Cubosomes</subject><subject>Cytotoxicity</subject><subject>Dentistry</subject><subject>Fatty Alcohols - pharmacology</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - metabolism</subject><subject>Liquid Crystals - chemistry</subject><subject>Mice</subject><subject>Microscopy, Confocal</subject><subject>Nanoparticles - ultrastructure</subject><subject>Particle Size</subject><subject>Phase behaviour</subject><subject>Phase Transition - drug effects</subject><subject>Phosphatidylserines - pharmacology</subject><subject>Phytantriol</subject><subject>Quartz Crystal Microbalance Techniques</subject><subject>Scattering, Small Angle</subject><subject>Small angle X-ray scattering</subject><subject>Static Electricity</subject><subject>Surface-Active Agents - pharmacology</subject><subject>Synchrotrons</subject><subject>Unilamellar Liposomes - chemistry</subject><subject>X-Ray Diffraction</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks-O1SAUh4nRONfRVzCNG1e9HmjhUhcmZvybTOLCcU0onOZypaUD7SR9Al9byB2NcaMrAv1-51C-Q8gLCnsKVLw67XsXRr1gdNqnPYP8AeQeGnhAdlQeZM074A_JDmjL6k5QdkGepHSCvIeWPSYXDKQELumO_Lg5YuWmwa84GazCUFk3az-6JWy-mo8hzUe9OLv5lNtNmZjyqU5Y9XjUdy6ssYT0ZCuD3q9exypimsOUkSVUfgtLDLMzlXe3q8tU3NKivS-1rEszxuQy_JQ8GvLP4LP79ZJ8-_D-5upTff3l4-ert9e1aYVY6q4XWurB9hZtZ601h8Z0HQNGuWmx7xvTDEB7ygbsOENudN8K2wxMNJJaIZpL8vJcd47hdsW0qNGlcnM9YViTkpwLKVvg_yQPomFcckoz-fpMmhhSijioObpRx01RUMWYOqk_jaliTIFU2VgOP79vs_Yj2t_RX4oy8O4MYH6WO4dRJeOKLOsimkXZ4P6vz5u_ypjswBntv-OG6ZRFTiVDVWIK1NcyO2V0aJ4a4Iw3PwExM8gZ</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>Shen, Hsin-Hui</creator><creator>Crowston, Jonathan G</creator><creator>Huber, Florian</creator><creator>Saubern, Simon</creator><creator>McLean, Keith M</creator><creator>Hartley, Patrick G</creator><general>Elsevier Ltd</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><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20101201</creationdate><title>The influence of dipalmitoyl phosphatidylserine on phase behaviour of and cellular response to lyotropic liquid crystalline dispersions</title><author>Shen, Hsin-Hui ; Crowston, Jonathan G ; Huber, Florian ; Saubern, Simon ; McLean, Keith M ; Hartley, Patrick G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-9b6a8afdbded9dddc73c9920215c4ebb3c3f01b12fe952e5cab46d3f26381d663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>Cell Death - drug effects</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>Confocal microscopy</topic><topic>Cubosomes</topic><topic>Cytotoxicity</topic><topic>Dentistry</topic><topic>Fatty Alcohols - pharmacology</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - metabolism</topic><topic>Liquid Crystals - chemistry</topic><topic>Mice</topic><topic>Microscopy, Confocal</topic><topic>Nanoparticles - ultrastructure</topic><topic>Particle Size</topic><topic>Phase behaviour</topic><topic>Phase Transition - drug effects</topic><topic>Phosphatidylserines - pharmacology</topic><topic>Phytantriol</topic><topic>Quartz Crystal Microbalance Techniques</topic><topic>Scattering, Small Angle</topic><topic>Small angle X-ray scattering</topic><topic>Static Electricity</topic><topic>Surface-Active Agents - pharmacology</topic><topic>Synchrotrons</topic><topic>Unilamellar Liposomes - chemistry</topic><topic>X-Ray Diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Hsin-Hui</creatorcontrib><creatorcontrib>Crowston, Jonathan G</creatorcontrib><creatorcontrib>Huber, Florian</creatorcontrib><creatorcontrib>Saubern, Simon</creatorcontrib><creatorcontrib>McLean, Keith M</creatorcontrib><creatorcontrib>Hartley, Patrick G</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><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Hsin-Hui</au><au>Crowston, Jonathan G</au><au>Huber, Florian</au><au>Saubern, Simon</au><au>McLean, Keith M</au><au>Hartley, Patrick G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The influence of dipalmitoyl phosphatidylserine on phase behaviour of and cellular response to lyotropic liquid crystalline dispersions</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>31</volume><issue>36</issue><spage>9473</spage><epage>9481</epage><pages>9473-9481</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Abstract Lyotropic liquid crystalline nanoparticles (cubosomes) have the potential to act as amphiphilic scaffolds for the presentation of lipids and subsequent application in, for example, bioseparations and therapeutic delivery. In this work we have formulated lyotropic liquid crystalline systems based on the synthetic amphiphile 1,2,3-trihydroxy-3,7,11,15-tetramethylhexadecane (phytantriol) and containing the lipid dipalmitoyl phosphatidylserine (DPPS). We have prepared a range of DPPS-containing phytantriol cubosome formulations and characterized them using Small Angle X-ray Scattering and Cryo-transmission electron microscopy. These techniques show that increased DPPS content induces marked changes in lyotropic liquid crystalline phase behaviour, characterized by changes in crystallographic dimensions and increases in vesicle content. Furthermore, in vitro cell culture studies indicate that these changes correlate with lipid/surfactant cellular uptake and cytotoxicity. A model cell membrane based on a surface supported phospholipid bilayer was used to gain insights into cubosome–bilayer interactions using Quartz Crystal Microgravimetry. The data show that mass uptake at the supported bilayer increased with DPPS content. We propose that the cytotoxicity of the DPPS-containing dispersions results from changes in lipid/surfactant phase behaviour and the preferential attachment and fusion of vesicles at the cell membrane.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>20880581</pmid><doi>10.1016/j.biomaterials.2010.08.030</doi><tpages>9</tpages></addata></record> |
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subjects | Advanced Basic Science Animals Cell Death - drug effects Cell Line Cell Survival - drug effects Confocal microscopy Cubosomes Cytotoxicity Dentistry Fatty Alcohols - pharmacology Fibroblasts - cytology Fibroblasts - drug effects Fibroblasts - metabolism Liquid Crystals - chemistry Mice Microscopy, Confocal Nanoparticles - ultrastructure Particle Size Phase behaviour Phase Transition - drug effects Phosphatidylserines - pharmacology Phytantriol Quartz Crystal Microbalance Techniques Scattering, Small Angle Small angle X-ray scattering Static Electricity Surface-Active Agents - pharmacology Synchrotrons Unilamellar Liposomes - chemistry X-Ray Diffraction |
title | The influence of dipalmitoyl phosphatidylserine on phase behaviour of and cellular response to lyotropic liquid crystalline dispersions |
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