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荷电微胶囊用于疏水性活性物质的控制释放 第二部分:通过 LbL 吸附和适当固定分散剂层上的脂质双层形成进行表面改性。

Charged microcapsules for controlled release of hydrophobic actives Part II: surface modification by LbL adsorption and lipid bilayer formation on properly anchored dispersant layers.

机构信息

Department of Chemical and Biological Engineering, Applied Surface Chemistry, Chalmers University of Technology, Göteborg, Sweden.

出版信息

J Colloid Interface Sci. 2013 Nov 1;409:8-17. doi: 10.1016/j.jcis.2013.06.070. Epub 2013 Jul 11.

Abstract

Charge microcapsules with a dodecane core and a poly(methyl methacrylate) (PMMA) shell have been prepared via the internal phase separation method using ionic dispersants. The microcapsules have subsequently been surface modified with polyelectrolyte multilayers and lipid bilayers. Two types of ionic dispersant systems have been investigated: a small set of ionic amphiphilic block copolymers of poly(methyl methacrylate)-block-poly(sodium (meth)acrylate) type and an oil-soluble anionic surfactant, sodium 1,5-dioxo-1,5-bis(3,5,5-trimethylhexyloxy)-3-((3,5,5trimethylhexyloxy)carbonyl)pentane-2-sulfonate, in combination with a water-soluble polycation, poly(diallyldimethylammonium chloride). The Layer-by-Layer adsorption of the polyelectrolyte pair poly(diallydimethylammonium chloride) (350,000 g/mol) and poly(sodium methacrylate) (15,000 g/mol) was successfully made on both microcapsule systems with the formation of very thin multilayers as indicated with quartz crystal microbalance with dissipation monitoring (QCM-D) measurements on model surfaces. Formation of a lipid bilayer on the surface of the microcapsules from liposomes with a charge opposite that of the capsule surface was also proven to be successful as indicated by the ζ-potential of the microcapsules, the characteristic frequency shift as measured with QCM-D and fluorescence recovery after photobleaching (FRAP) on model systems. However, the proper anchorage of the dispersants in the underlying PMMA surface was key for the successful surface modification.

摘要

用离子分散剂通过内相分离法制备了具有十二烷核和聚甲基丙烯酸甲酯 (PMMA) 壳的带电微胶囊。随后,用聚电解质层层和脂质双层对微胶囊进行了表面改性。研究了两种类型的离子分散剂体系:一组较小的聚甲基丙烯酸甲酯嵌段-聚(甲基丙烯酸)嵌段型离子两亲嵌段共聚物和油溶性阴离子表面活性剂,1,5-二氧代-1,5-双(3,5,5-三甲基己氧基)-3-((3,5,5-三甲基己氧基)羰基)戊烷-2-磺酸钠,与水溶性聚阳离子,聚二烯丙基二甲基氯化铵结合。聚电解质对聚二烯丙基二甲基氯化铵(350,000 g/mol)和聚(甲基丙烯酸)(15,000 g/mol)的层层吸附在两种微胶囊体系上均成功进行,如石英晶体微天平耗散监测(QCM-D)在模型表面上的测量所示,形成了非常薄的多层。如微胶囊的 ζ-电位、QCM-D 测量的特征频率偏移以及模型系统上光漂白后荧光恢复(FRAP)所示,成功地在微胶囊表面上从带相反电荷的脂质体形成脂质双层。然而,分散剂在底层 PMMA 表面的适当锚定是成功表面改性的关键。

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