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
Hauptverfasser: Shen, Hsin-Hui, Crowston, Jonathan G, Huber, Florian, Saubern, Simon, McLean, Keith M, Hartley, Patrick G
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container_end_page 9481
container_issue 36
container_start_page 9473
container_title Biomaterials
container_volume 31
creator Shen, Hsin-Hui
Crowston, Jonathan G
Huber, Florian
Saubern, Simon
McLean, Keith M
Hartley, Patrick G
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. 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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. 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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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