Advances in the Structural Design of Polyelectrolyte Complex Micelles

被引:48
|
作者
Marras, Alexander E. [1 ]
Ting, Jeffrey M. [1 ,2 ]
Stevens, Kaden C. [1 ]
Tirrell, Matthew, V [1 ]
机构
[1] Univ Chicago, Pritzker Sch Mol Engn, Chicago, IL 60637 USA
[2] 3M Co, 3M Ctr, St Paul, MN 55144 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2021年 / 125卷 / 26期
关键词
DIBLOCK COPOLYMER MICELLES; CHARGED BLOCK-COPOLYMERS; COACERVATE CORE MICELLES; DRUG-DELIVERY; CATIONIC COPOLYMERS; POLYPLEX MICELLES; INTRACELLULAR DELIVERY; POLYMERIC MICELLES; PERSISTENCE LENGTH; IONOMER COMPLEXES;
D O I
10.1021/acs.jpcb.1c01258
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Polyelectrolyte complex micelles (PCMs) are a unique class of self-assembled nanoparticles that form with a core of associated polycations and polyanions, microphase-separated from neutral, hydrophilic coronas in aqueous solution. The hydrated nature and structural and chemical versatility make PCMs an attractive system for delivery and for fundamental polymer physics research. By leveraging block copolymer design with controlled self-assembly, fundamental structure-property relationships can be established to tune the size, morphology, and stability of PCMs precisely in pursuit of tailored nanocarriers, ultimately offering storage, protection, transport, and delivery of active ingredients. This perspective highlights recent advances in predictive PCM design, focusing on (i) structure-property relationships to target specific nanoscale dimensions and shapes and (ii) characterization of PCM dynamics primarily using time-resolved scattering techniques. We present several vignettes from these two emerging areas of PCM research and discuss key opportunities for PCM design to advance precision medicine.
引用
收藏
页码:7076 / 7089
页数:14
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