The Impact of Lipid Digestion on the Dynamic and Structural Properties of Micelles

被引:6
|
作者
Pink, Demi L. [1 ]
Foglia, Fabrizia [2 ]
Barlow, David J. [3 ]
Lawrence, M. Jayne [4 ]
Lorenz, Christian D. [1 ]
机构
[1] Kings Coll London, Dept Phys, London WC2R 2LS, England
[2] UCL, Dept Chem, 20 Gordon St, London WC1H 0AJ, England
[3] Kings Coll London, Fac Life Sci & Med, Franklin Wilkins Bldg,Stamford St, London SE1 9NH, England
[4] Univ Manchester, Fac Biol Med & Hlth, Sch Hlth Sci, Div Pharm & Optometry, Stopford Bldg,Oxford Rd, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会; 美国国家科学基金会; 欧盟地平线“2020”;
关键词
drug delivery vehicles; lipid digestion; lipid micelles; molecular dynamics simulations; phosphocholine lipids; small-angle neutron scattering; FATTY-ACIDS; LYSOPHOSPHATIDYLCHOLINES; PHOSPHATIDYLCHOLINE; PHOSPHOLIPASE-A2; EFFICIENT; BEHAVIOR; ORIGIN; PHASE; FIELD;
D O I
10.1002/smll.202004761
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-assembled, lipid-based micelles, such as those formed by the short-chain phosphocholine, dihexanoylphosphatidylcholine (2C6PC), are degraded by the pancreatic enzyme, phospholipase A(2) (PLA2). Degradation yields 1-hexanoyl-lysophosphocholine (C6LYSO) and hexanoic acid (C6FA) products. However, little is known about the behavior of these products during and after the degradation of 2C6PC. In this work, a combination of static and time-resolved small angle neutron scattering, as well as all-atom molecular dynamics simulations, is used to characterize the structure of 2C6PC micelles. In doing so a detailed understanding of the substrate and product aggregation behavior before, during and after degradation is gained. Consequently, the formation of mixed micelles containing 2C6PC, C6LYSO and C6FA is shown at every stage of the degradation process, as well as the formation of mixed C6LYSO/C6FA micelles after degradation is complete. The use of atomistic molecular dynamics has allowed us to characterize the structure of 2C6PC, 2C6PC/C6LYSO/C6FA, and C6LYSO/C6FA micelles throughout the degradation process, showing the localization of the different molecular species within the aggregates. In addition, the hydration of the 2C6PC, C6LYSO, and C6FA species both during micellization and as monomers in aqueous solution is documented to reveal the processes driving their micellization.
引用
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页数:11
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