Effect of surfactant on unilamellar polymeric vesicles: Altered membrane properties and stability in the limit of weak surfactant partitioning

被引:31
作者
Santore, MM [1 ]
Discher, DE
Won, YY
Bates, FS
Hammer, DA
机构
[1] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
[2] Univ Penn, Dept Chem Engn, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Mech Engn, Philadelphia, PA 19104 USA
[4] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[5] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
关键词
D O I
10.1021/la0201319
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surfactant incorporation into bilayer vesicle membranes made of diblock copolymers was examined for the case of weak affinity between the membrane [poly(ethyl ethylene)-co-poly(ethylene oxide)] and the surfactant [Pluronic L31]. For copolymer vesicles formed in the absence of surfactant and subsequently exposed to surfactant solutions, a micropipet aspiration technique was employed to monitor surfactant incorporation kinetics and to characterize surfactant-induced changes in the membranes. Though the surfactant incorporation was weak and reversible, it reduced, the area expansion modulus by almost a factor of 2, while dramatically increasing the vesicles' susceptibility-to lysis. Additionally, water permeability was increased by a factor of 2. The surfactant incorporation rates were proportional to the free surfactant concentration, and other features of the membrane response to surfactant exposure were consistent with transport-limited surfactant attack of the membranes. The most plausible mechanism for surfactant interaction with the membrane is that the surfactant resides at the interface between the hydrophobic membrane core and the poly(ethylene oxide) corona, reducing the interfacial tension of the lamella and allowing the membrane to thin slightly, also increasing its area per unit mass. Observations suggest slow surfactant penetration of the hydrophobic core such that this particular surfactant acts on both inner and outer leaflets.
引用
收藏
页码:7299 / 7308
页数:10
相关论文
共 39 条
[1]   Electromechanical limits of polymersomes [J].
Aranda-Espinoza, H ;
Bermudez, H ;
Bates, FS ;
Discher, DE .
PHYSICAL REVIEW LETTERS, 2001, 87 (20) :208301-1
[2]   Two photon fluorescence microscopy of coexisting lipid domains in giant unilamellar vesicles of binary phospholipid mixtures [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :290-305
[3]   Immobilization in surface-tethered lipid vesicles as a new tool for single biomolecule spectroscopy [J].
Boukobza, E ;
Sonnenfeld, A ;
Haran, G .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (48) :12165-12170
[4]  
CARSLAW HS, 1941, OPERATIONAL METHODS, P247
[5]  
COHENSTUART MA, 1984, MACROMOLECULES, V17, P1825
[6]   KINETICS OF POLYMER ADSORPTION AND DESORPTION IN CAPILLARY-FLOW [J].
DIJT, JC ;
STUART, MAC ;
FLEER, GJ .
MACROMOLECULES, 1992, 25 (20) :5416-5423
[7]   Polymersomes: Tough vesicles made from diblock copolymers [J].
Discher, BM ;
Won, YY ;
Ege, DS ;
Lee, JCM ;
Bates, FS ;
Discher, DE ;
Hammer, DA .
SCIENCE, 1999, 284 (5417) :1143-1146
[8]   Polymer vesicles in various media [J].
Discher, BM ;
Hammer, DA ;
Bates, FS ;
Discher, DE .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2000, 5 (1-2) :125-131
[9]   PHYSICAL-PROPERTIES OF SURFACTANT BILAYER-MEMBRANES - THERMAL TRANSITIONS, ELASTICITY, RIGIDITY, COHESION, AND COLLOIDAL INTERACTIONS [J].
EVANS, E ;
NEEDHAM, D .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (16) :4219-4228
[10]   Poly(ethylene oxide) adsorption onto chemically etched silicates by Brewster angle reflectivity [J].
Fu, ZG ;
Santore, MM .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1998, 135 (1-3) :63-75