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反双连续立方中间相相互转化的动力学及机理

Kinetics and mechanism of the interconversion of inverse bicontinuous cubic mesophases.

作者信息

Squires Adam M, Templer R H, Seddon J M, Woenkhaus J, Winter R, Narayanan T, Finet S

机构信息

Cavendish Laboratory, Cambridge Universit, UK.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2005 Jul;72(1 Pt 1):011502. doi: 10.1103/PhysRevE.72.011502. Epub 2005 Jul 11.

Abstract

This paper describes time-resolved x-ray diffraction data monitoring the transformation of one inverse bicontinuous cubic mesophase into another, in a hydrated lipid system. The first section of the paper describes a mechanism for the transformation that conserves the topology of the bilayer, based on the work of Charvolin and Sadoc, Fogden and Hyde, and Benedicto and O'Brien in this area. We show a pictorial representation of this mechanism, in terms of both the water channels and the lipid bilayer. The second section describes the experimental results obtained. The system under investigation was 2:1 lauric acid: dilauroylphosphatidylcholine at a hydration of 50% water by weight. A pressure-jump was used to induce a phase transition from the gyroid (Q(G)(II)) to the diamond (Q(D)(II)) bicontinuous cubic mesophase, which was monitored by time-resolved x-ray diffraction. The lattice parameter of both mesophases was found to decrease slightly throughout the transformation, but at the stage where the Q (D)(II) phase first appeared, the ratio of lattice parameters of the two phases was found to be approximately constant for all pressure-jump experiments. The value is consistent with a topology-preserving mechanism. However, the polydomain nature of our sample prevents us from confirming that the specific pathway is that described in the first section of the paper. Our data also reveal signals from two different intermediate structures, one of which we have identified as the inverse hexagonal (H(II)) mesophase. We suggest that it plays a role in the transfer of water during the transformation. The rate of the phase transition was found to increase with both temperature and pressure-jump amplitude, and its time scale varied from the order of seconds to minutes, depending on the conditions employed.

摘要

本文描述了在水合脂质体系中,利用时间分辨X射线衍射数据监测一种反相双连续立方中间相转变为另一种中间相的过程。论文的第一部分基于Charvolin和Sadoc、Fogden和Hyde以及Benedicto和O'Brien在该领域的研究成果,描述了一种保持双层拓扑结构的转变机制。我们展示了该机制在水通道和脂质双层方面的图示。第二部分描述了所获得的实验结果。所研究的体系是月桂酸与二月桂酰磷脂酰胆碱按2:1的比例,水合程度为50%(重量)。通过压力跃升诱导从类螺旋体(Q(G)(II))到菱形(Q(D)(II))双连续立方中间相的相变,并用时间分辨X射线衍射进行监测。发现在整个转变过程中,两种中间相的晶格参数均略有下降,但在Q(D)(II)相首次出现的阶段,所有压力跃升实验中发现两种相的晶格参数之比大致恒定。该值与拓扑保持机制一致。然而,我们样品的多畴性质使我们无法确定具体途径是否如论文第一部分所述。我们的数据还揭示了来自两种不同中间结构的信号,其中一种我们已确定为反相六角(H(II))中间相。我们认为它在转变过程中的水传递中起作用。发现相变速率随温度和压力跃升幅度的增加而增加,其时间尺度从几秒到几分钟不等,具体取决于所采用的条件。

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