Adsorption behaviors of DPPC/MO aggregates on SiO2 surfaces

The adsorption kinetics of extruded 1,2-dipalmitoyl- sn-glycero-3-phosphatidylcholine (DPPC)/1-(cis-9-octadecenoyl)- rac-glycerol (monoolein, MO) aggregates on SiO 2 surface at 25 degrees C is investigated in real time, using the dissipative quartz crystal microbalance (QCM) technique. Four adsorpti...

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Publié dans:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 24(2008), 20 vom: 21. Okt., Seite 11616-24
Auteur principal: Wang, Zhining (Auteur)
Autres auteurs: Yang, Shihe
Format: Article en ligne
Langue:English
Publié: 2008
Accès à la collection:Langmuir : the ACS journal of surfaces and colloids
Sujets:Journal Article
Description
Résumé:The adsorption kinetics of extruded 1,2-dipalmitoyl- sn-glycero-3-phosphatidylcholine (DPPC)/1-(cis-9-octadecenoyl)- rac-glycerol (monoolein, MO) aggregates on SiO 2 surface at 25 degrees C is investigated in real time, using the dissipative quartz crystal microbalance (QCM) technique. Four adsorption pathways have been identified depending on the molar fraction of MO in the DPPC/MO system: (I) intact vesicle adsorption, (II) vesicle reorganization on a SiO 2 surface, (III) supported lipid bilayer (SLB) formation, and (IV) cubosome adsorption. The results can be understood by the fact that DPPC is a lamellar phase-forming lipid, whereas MO prefers the cubic phase. Therefore, the incorporation of MO in DPPC increases the packing parameter. Equally important, MO also increases the mobility of lipid molecules and lateral pressure in the bilayers as a result of the presence of a unique cis- double bond. Before extrusion, the vesicles size increases with the MO content when X MO <or= 0.7 and cubosomes are formed for X MO >or= 0.8. The extruded DPPC/MO suspensions consist of reformed vesicles for X MO <or= 0.7 and filtered cubosomes for X MO >or= 0.8, all with a uniform diameter of approximately 100 nm. Differential scanning calorimetry (DSC) further indicates that the addition of MO lowers the main phase transition temperature of DPPC and thus makes the hydrophobic interior more fluid
Description:Date Completed 13.11.2008
Date Revised 16.10.2008
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1520-5827
DOI:10.1021/la801723j