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小角中子散射研究脂质体温度诱导的结构变化。

Small-Angle Neutron Scattering Study of Temperature-Induced Structural Changes in Liposomes.

机构信息

Biomaterials Science Center, Department of Biomedical Engineering , University of Basel , Allschwil 4123 , Switzerland.

Laboratory for Neutron Scattering and Imaging , Paul Scherrer Institute , Villigen PSI 5232 , Switzerland.

出版信息

Langmuir. 2019 Aug 27;35(34):11210-11216. doi: 10.1021/acs.langmuir.9b01603. Epub 2019 Aug 13.

DOI:10.1021/acs.langmuir.9b01603
PMID:31343180
Abstract

Liposomes of specific artificial phospholipids, such as Pad-PC-Pad and Rad-PC-Rad, are mechanically responsive. They can release encapsulated therapeutics via physical stimuli, as naturally present in blood flow of constricted vessel segments. The question is how these synthetic liposomes change their structure in the medically relevant temperature range from 22 to 42 °C. In the present study, small-angle neutron scattering (SANS) was employed to evaluate the temperature-induced structural changes of selected artificial liposomes. For Rad-PC-Rad, Pad-Pad-PC, Sur-PC-Sur, and Sad-PC-Sad liposomes, the SANS data have remained constant because the phase transition temperatures are above 42 °C. For Pad-PC-Pad and Pes-PC-Pes liposomes, whose phase transitions are below 42 °C, the -plots have revealed temperature-dependent structural changes. The average diameter of Pad-PC-Pad liposomes remained almost constant, whereas the eccentricity decreased by an order of magnitude. Related measurements using transmission electron microscopy at cryogenic temperatures, as well as dynamic light scattering before and after the heating cycles, underpin the fact that the non-spherical liposomes flatten out. The SANS data further indicated that, as a consequence of the thermal loop, the mean bilayer thickness increased by 20%, associated with the loss of lipid membrane interdigitation. Therefore, Pad-PC-Pad liposomes are unsuitable for local drug delivery in the atherosclerotic human blood vessel system. In contrast, Rad-PC-Rad liposomes are thermally stable for applications within the human body.

摘要

特定人工磷脂的脂质体,如 Pad-PC-Pad 和 Rad-PC-Rad,具有机械响应性。它们可以通过物理刺激释放包裹的治疗药物,就像在血管狭窄段的血流中自然存在的那样。问题是这些合成脂质体在医学相关的温度范围内(22 至 42°C)如何改变其结构。在本研究中,小角中子散射(SANS)被用于评估选定的人工脂质体的温度诱导结构变化。对于 Rad-PC-Rad、Pad-Pad-PC、Sur-PC-Sur 和 Sad-PC-Sad 脂质体,SANS 数据保持不变,因为相变温度高于 42°C。对于 Pad-PC-Pad 和 Pes-PC-Pes 脂质体,其相变温度低于 42°C,-图揭示了温度依赖性的结构变化。Pad-PC-Pad 脂质体的平均直径几乎保持不变,而偏心率降低了一个数量级。在低温下使用透射电子显微镜进行的相关测量,以及加热循环前后的动态光散射,证实了非球形脂质体变平的事实。SANS 数据还表明,由于热循环,双层膜厚度平均增加了 20%,同时脂质膜的互穿性丧失。因此,Pad-PC-Pad 脂质体不适合用于动脉粥样硬化人类血管系统中的局部药物输送。相比之下,Rad-PC-Rad 脂质体在人体应用中具有热稳定性。

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