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Revealing the Structural Intricacies of Biomembrane-Interfaced Emulsions with Small- and Ultra-Small-Angle Neutron Scattering.
Vidallon, Mark Louis P; Williams, Ashley P; Moon, Mitchell J; Liu, Haikun; Trépout, Sylvain; Bishop, Alexis I; Teo, Boon Mian; Tabor, Rico F; Peter, Karlheinz; de Campo, Liliana; Wang, Xiaowei.
Afiliación
  • Vidallon MLP; Molecular Imaging and Theranostics Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC, 3004, Australia.
  • Williams AP; Baker Department of Cardiometabolic Health, University of Melbourne, Parkville, VIC, 3010, Australia.
  • Moon MJ; School of Chemistry, Monash University, Clayton, VIC, 3800, Australia.
  • Liu H; Baker Department of Cardiovascular Research, Translation and Implementation, La Trobe University, Bundoora, VIC, 3086, Australia.
  • Trépout S; School of Chemistry, Monash University, Clayton, VIC, 3800, Australia.
  • Bishop AI; Baker Department of Cardiometabolic Health, University of Melbourne, Parkville, VIC, 3010, Australia.
  • Teo BM; Atherothrombosis and Vascular Biology Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC, 3004, Australia.
  • Tabor RF; Molecular Imaging and Theranostics Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC, 3004, Australia.
  • Peter K; Baker Department of Cardiometabolic Health, University of Melbourne, Parkville, VIC, 3010, Australia.
  • de Campo L; Ramaciotti Centre for Cryo-Electron Microscopy, Monash University, Clayton, VIC, 3800, Australia.
  • Wang X; School of Physics and Astronomy, Monash University, Clayton, VIC, 3800, Australia.
Small Methods ; : e2400348, 2024 Aug 01.
Article en En | MEDLINE | ID: mdl-39087373
ABSTRACT
Utilizing cell membranes from diverse cell types for biointerfacing has demonstrated significant advantages in enhancing colloidal stability and incorporating biological properties, tailored specifically for various biomedical applications. However, the structures of these materials, particularly emulsions interfaced with red blood cell (RBC) or platelet (PLT) membranes, remain an underexplored area. This study systematically employs small- and ultra-small-angle neutron scattering (SANS and USANS) with contrast variation to investigate the structure of emulsions containing perfluorohexane within RBC (RBC/PFH) and PLT membranes (PLT/PFH). The findings reveal that the scattering length density of RBC and PLT membranes is 1.5 × 10-6 Å-2, similar to 30% (w/w) deuterium oxide. Using this solvent as a cell membrane-matching medium, estimated droplet diameters are 770 nm (RBC/PFH) and 1.5 µm (PLT/PFH), based on polydispersed sphere model fitting. Intriguingly, calculated patterns and invariant analysis reveal native droplet architectures featuring entirely liquid PFH cores, differing significantly from the observed bubble-droplet core system in electron microscopy. This highlights the advantage of SANS and USANS in differentiating genuine colloidal structures in complex dispersions. In summary, this work underscores the pivotal role of SANS and USANS in characterizing biointerfaced colloids and in uncovering novel colloidal structures with significant potential for biomedical applications and clinical translation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Small Methods Año: 2024 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Small Methods Año: 2024 Tipo del documento: Article País de afiliación: Australia