Interparticle Interactions in Dilute Solutions of Polyelectrolyte Complex Micelles [electronic resource]

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Tác giả:

Ngôn ngữ: eng

Ký hiệu phân loại: 541.3 Miscellaneous topics in physical chemistry

Thông tin xuất bản: Oak Ridge, Tenn. : Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy, 2019

Mô tả vật lý: Size: p. 819-825 : , digital, PDF file.

Bộ sưu tập: Metadata

ID: 259995

 The application of dilute solutions of polyelectrolyte complex (PEC) micelles for delivering therapeutic nucleic acids into disease sites has gained momentum. This Letter reports a detailed characterization of PEC micelles in dilute solutions including their internal structures and the determination of the interparticle interactions. The polymer concentration ranges from 0.1 to 0.5 wt %, a regime where micelle?micelle interactions are infrequent. We employ synchrotron small-angle X-ray scattering (SAXS) to simultaneously probe the morphology, internal structure, and radius of gyration (R<
 sub>
 g<
 /sub>
 ) of the self-assemblies formed by charged diblock polyelectrolytes and homopolyelectrolytes. The emerging appearance of the structure factor in SAXS profiles with the increasing polymer concentration demonstrates the presence of the repulsive intermicellar correlations, which is further confirmed by the differences between the ?reciprocal R<
 sub>
 g<
 /sub>
 ? estimated by Guinier approximation and the ?real space R<
 sub>
 g<
 /sub>
 ? determined by pair distribution functions. We find that the soft corona chains tethered on the surface of phase-separated complex domains are compressed when micelles come close to the point where a hard-sphere interaction takes over. These findings contribute to the fundamental understanding of the structure and space-filling constraints in the complexation-driven self-assemblies and advance the rational design of cationic polymer-based nonviral gene delivery vectors.
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