Self-Assembled Block Polymer Aggregates in Selective Solution: Controllable Morphology Transitions and their Applications in Drug Delivery
Abstract
Introduction: Amphiphilic block copolymers are able to self-assemble into rich morphologies with high controllability for drug delivery. Great efforts have been made for decades to construct efficient drug delivery systems (DDSs) using nanostructured self-assemblies to overcome the drawbacks of pharmaceuticals, such as low aqueous solubility, premature drug release during circulation, and undesirable side effects. Areas covered: Here we review the researches of self-assembled block polymer aggregates with a focus on the shape-forming and shape-changing mechanisms, and applications of controlling morphology transition by multiple factors in drug delivery. We tend to provide a comprehensive description of the connection between structure-changing thermodynamics, kinetics, and influencing factors, thus to enlighten more pathways for future developments in the field of drug delivery. Expert opinion: By understanding the underlying mechanisms for the structure formation and transition, it enables versatile applications in DDSs design by altering drug morphologies. However, developing more sophisticated and multifunctional polymeric nanocarriers is still challengeable in the clinical application, which would hold considerable potential in promoting the efficiency in morphology control to achieve higher intelligence of drug delivery.
Recommended Citation
W. Jiao et al., "Self-Assembled Block Polymer Aggregates in Selective Solution: Controllable Morphology Transitions and their Applications in Drug Delivery," Expert Opinion on Drug Delivery, vol. 17, no. 7, pp. 947 - 961, Taylor & Francis, Jul 2020.
The definitive version is available at https://doi.org/10.1080/17425247.2020.1767582
Department(s)
Chemical and Biochemical Engineering
Keywords and Phrases
block copolymers; Drug delivery; morphology transition; self-assembly
International Standard Serial Number (ISSN)
1742-5247; 1744-7593
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2020 Taylor & Francis, All rights reserved.
Publication Date
01 Jul 2020
PubMed ID
32441156