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Miscibility and Phase Behavior of N-Acylethanolamine/Diacylphosphatidylethanolamine Binary Mixtures of Matched Acyl Chainlengths (n = 14, 16)

机译:匹配酰基链长度的N-酰基乙醇胺/二酰基磷脂酰乙醇胺二元混合物的相溶性和相行为(n = 14,16)

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摘要

The miscibility and phase behavior of hydrated binary mixtures of two N-acylethanolamines (NAEs), N-myristoylethanolamine (NMEA), and N-palmitoylethanolamine (NPEA), with the corresponding diacyl phosphatidylethanolamines (PEs), dimyristoylphosphatidylethanolamine (DMPE), and dipalmitoylphosphatidylethanolamine (DPPE), respectively, have been investigated by differential scanning calorimetry (DSC), spin-label electron spin resonance (ESR), and 31P-NMR spectroscopy. Temperature-composition phase diagrams for both NMEA/DMPE and NPEA/DPPE binary systems were established from high sensitivity DSC. The structures of the phases involved were determined by 31P-NMR spectroscopy. For both systems, complete miscibility in the fluid and gel phases is indicated by DSC and ESR, up to 35 mol % of NMEA in DMPE and 40 mol % of NPEA in DPPE. At higher contents of the NAEs, extensive solid-fluid phase separation and solid-solid immiscibility occur depending on the temperature. Characterization of the structures of the mixtures formed with 31P-NMR spectroscopy shows that up to 75 mol % of NAE, both DMPE and DPPE form lamellar structures in the gel phase as well as up to at least 65°C in the fluid phase. ESR spectra of phosphatidylcholine spin labeled at the C-5 position in the sn-2 acyl chain present at a probe concentration of 1 mol % exhibit strong spin-spin broadening in the low-temperature region for both systems, suggesting that the acyl chains pack very tightly and exclude the spin label. However, spectra recorded in the fluid phase do not exhibit any spin-spin broadening and indicate complete miscibility of the two components. The miscibility of NAE and diacyl PE of matched chainlengths is significantly less than that found earlier for NPEA and dipalmitoylphosphatidylcholine, an observation that is consistent with the notion that the NAEs are most likely stored as their precursor lipids (N-acyl PEs) and are generated only when the system is subjected to membrane stress.
机译:两种N-酰基乙醇胺(NAE),N-肉豆蔻基乙醇胺(NMEA)和N-棕榈酰乙醇胺(NPEA)与相应的二酰基磷脂酰乙醇胺(PEs),二肉豆蔻酰基磷脂酰乙醇胺(DMPE)和二棕榈酰磷酸(DMPE)的水合二元混合物的混溶性和相行为DPPE)分别通过差示扫描量热法(DSC),自旋标记电子自旋共振(ESR)和31P-NMR光谱进行了研究。 NMEA / DMPE和NPEA / DPPE二元系统的温度组成相图均由高灵敏度DSC建立。通过31P-NMR光谱确定所涉及的相的结构。对于这两种系统,DSC和ESR均表明了其在液相和凝胶相中的完全混溶性,DMPE中的NMEA含量高达35 mol%,DPPE中的NPEA含量高达40 mol%。在较高的NAE含量下,取决于温度,会发生广泛的固液相分离和固固不混溶。用31 P-NMR光谱形成的混合物的结构表征表明,高达75 mol%的NAE,DMPE和DPPE均在凝胶相中形成层状结构,而在液相中则至少达到65°C。探针浓度为1 mol%时出现在sn-2酰基链中C-5位置的磷脂酰胆碱自旋标记的ESR谱图显示,两种系统在低温区域均具有很强的自旋自旋加宽,表明该酰基链堆积非常紧密,并排除旋转标签。但是,在液相中记录的光谱没有表现出任何自旋-自旋加宽,并且表明了这两种组分的完全可混溶性。匹配链长的NAE和二酰基PE的可混溶性比之前发现的NPEA和二棕榈酰磷脂酰胆碱的可混溶性小得多,这一观察结果与NAE最有可能以其前体脂质(N-酰基PE)储存并产生的观点相一致仅当系统承受膜应力时。

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