4.5 Article

Liquid Surface X-ray Studies of Gold Nanoparticle-Phospholipid Films at the Air/Water Interface

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 120, Issue 34, Pages 9132-9141

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.6b03734

Keywords

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Funding

  1. National Science Foundation through the MRSEC program at the University of Chicago [DMR-1420709]
  2. NSF [MCB-1413613]
  3. National Science Foundation [NSF/CHE-1346572]
  4. DOE Office of Science [DE-AC02-06CH11357]
  5. Division Of Chemistry
  6. Direct For Mathematical & Physical Scien [1346572] Funding Source: National Science Foundation

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Amphiphilic phospholipids and nanoparticles functionalized with hydrophobic capping ligands have been extensively investigated for their capacity to self-assemble into Langmuir monolayers at the air/water interface. However, understanding of composite films consisting of both nano particles and phospholipids, and by extension, the complex interactions arising between nanomaterials and biological membranes, remains limited. In this work, dodecanethiol-capped gold nanoparticles (Au-NPs) with an average core diameter of 6 nm were incorporated into 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) monolayers with surface densities ranging from 0.1 to 20% area coverage at a surface pressure of 30 mN/m. High resolution liquid surface X-ray scattering studies revealed a phase separation of the DPPC and Au-NP components of the composite film, as confirmed with atomic force microscopy after the film was transferred to a substrate. At low Au-NP content, the structural organization of the phase-separated film is best described as a DPPC film containing isolated islands of Au-NPs. However, increasing the Au-NP content beyond 5% area coverage transforms the structural organization of the composite film to a long-range interconnected network of Au-NP strands surrounding small seas of DPPC, where the density of the Au-NP network increases with increasing Au-NP content. The observed phase separation and structural organization of the phospholipid and nanoparticle components in these Langmuir monolayers are useful for understanding interactions of nanoparticles with biological membranes.

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