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Application of spin markers for study of liposome prepared by the modified reverse-phase evaporation method

机译:旋转标记在研究改良反相蒸发法制备脂质体中的应用

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摘要

The EPR spectroscopy was used to determine the structure and physicochemical properties of liposomes prepared from L-alpha-phosphatidylcholine dipalmitoyl (DPPC) by the modified reverse-phase evaporation method (mREV). EPR study was carried out in the temperature range from 297 K to 340 K i. e. below and above the phase transition temperature T-C of DPPC. On the basis of EPR spectra of spin marker 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) incorporated into the liposome, the parameter f was determined. TEMPO dissolves easily in water and in the fluid lamellar smectic liquid-crystaline phase of lipid bilayer but is largely excluded from the solid, gel-phase. Thus TEMPO can be used to observe the change in the partition between aqueous and fluid lipid regions. The change in the relative value of f as a function of temperature for DPPC shows that, in the presence of water excess, this phospholipids undergoes a transition from a "gel phase" to a lamellar smectic liquid crystalline phase. On the basis of EPR spectra of spin marker 2-(3carboxypropyl)-4,4-dimethyl-2-tridecyl-3-oxazolidinloxyl (5-DOXYL) incorporated into liposome, the parameter a(N)' was determined. The isotropic N-14-hyperfine coupling constant a(N)' of nitroxide spin label depends on the local environmental polarity. The increase of a(N)' value reflects the rise of polarity of spin label environment. Temperature, cholesterol and pH dependent structural changes were also described.
机译:EPR光谱用于确定L-α-磷脂酰胆碱二棕榈酰(DPPC)通过改进的反相蒸发法(mREV)制备的脂质体的结构和理化性质。 EPR研究在297 K至340 K i的温度范围内进行。 e。低于和高于DPPC的相变温度T-C。根据掺入脂质体中的自旋标记2,2,6,6-四甲基-1-哌啶基氧基(TEMPO)的EPR光谱,确定参数f。 TEMPO易溶于水和脂质双层的层状近晶液晶相,但在固态,凝胶相中被大量排除。因此,TEMPO可用于观察水性脂质区域和流体脂质区域之间的分区变化。对于DPPC,f的相对值随温度的变化表明,在过量水存在下,该磷脂经历了从“凝胶相”到层状近晶液晶相的转变。根据掺入脂质体中的自旋标记物2-(3羧丙基)-4,4-二甲基-2-十三烷基-3-恶唑烷二氧戊烯基(5-DOXYL)的EPR光谱,确定参数a(N)'。一氧化氮自旋标记的各向同性N-14-超细偶合常数a(N)'取决于局部环境极性。 a(N)'值的增加反映了自旋标记环境极性的增加。还描述了温度,胆固醇和pH依赖的结构变化。

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