Diffusion behavior of lipid vesicles in entangled polymer solutions

被引:14
作者
Cao, XX
Bansil, R
Gantz, D
Moore, EW
Niu, N
Afdhal, NH
机构
[1] BOSTON UNIV,DEPT PHYS,CTR POLYMER STUDIES,BOSTON,MA 02215
[2] BOSTON UNIV,DEPT CHEM,BOSTON,MA 02215
[3] BOSTON UNIV,SCH MED,DEPT BIOPHYS,BOSTON,MA 02118
[4] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,RICHMOND,VA 23298
[5] BOSTON CITY HOSP,DEPT MED,GASTROENTEROL SECT,BOSTON,MA 02118
[6] BOSTON CITY HOSP,THORNDIKE MEM LABS,BOSTON,MA 02118
关键词
D O I
10.1016/S0006-3495(97)78224-9
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Dynamic light scattering was used to follow the tracer diffusion of phospholipid/cholesterol vesicles in aqueous polyacrylamide solutions and compared with the diffusive behavior of polystyrene (PS) latex spheres of comparable diameters. Over the range of the matrix concentration examined (C-p = 0.1-10 mg/ml), the diffusivities of the PS spheres and the large multilamellar vesicles exhibited the Stokes-Einstein (SE) relation, while the diffusivity of the unilamellar vesicles did not follow the increase of the solution's viscosity caused by the presence of the matrix molecules. The difference between the diffusion behaviors of unilamellar vesicles and hard PS spheres of similar size is possibly due to the flexibility of the lipid bilayer of the vesicles. The unilamellar vesicles are capable of changing their shape to move through the entangled polymer solution so that the hindrance to their diffusion due to the presence of the polymer chains is reduced, while the rigid PS spheres have little flexibility and they encounter greater resistance. The multilamellar vesicles are less flexible, thus their diffusion is similar to the hard PS spheres of similar diameter.
引用
收藏
页码:1932 / 1939
页数:8
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