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

Langmuir

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

Published: August 2019

AI Article Synopsis

  • Specific artificial phospholipids like Pad-PC-Pad and Rad-PC-Rad are shown to respond to mechanical stimuli and can release drugs under certain conditions mimicking blood flow.
  • Small-angle neutron scattering (SANS) was used to analyze how these liposomes' structures shift with temperature changes from 22 to 42 °C.
  • While Rad-PC-Rad liposomes remain stable for use in the human body, Pad-PC-Pad liposomes undergo unfavorable structural changes, making them less suitable for delivering medication in atherosclerotic blood vessels.

Article 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.

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Source
http://dx.doi.org/10.1021/acs.langmuir.9b01603DOI Listing

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