Stabilization of Lysozyme-Incorporated Polyion Complex Micelles by the ω-End Derivatization of Poly(ethylene glycol)−Poly(α,β-aspartic acid) Block Copolymers with Hydrophobic Groups-Reference-Cited by-同舟云学术

Stabilization of Lysozyme-Incorporated Polyion Complex Micelles by the ω-End Derivatization of Poly(ethylene glycol)−Poly(α,β-aspartic acid) Block Copolymers with Hydrophobic Groups

Published:2005-02-12 Issue:7 Volume:21 Page:2668-2674
ISSN:0743-7463
Container-title:Langmuir
language:en
Short-container-title:Langmuir

Author:

Yuan Xiaofei¹,Harada Atsushi¹,Yamasaki Yuichi¹,Kataoka Kazunori¹

Affiliation:

1. Department of Materials Engineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan, Department of Applied Materials Science, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Sakai, Osaka 599-8531, Japan, and Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Publisher

American Chemical Society (ACS)

Subject

Electrochemistry,Spectroscopy,Surfaces and Interfaces,Condensed Matter Physics,General Materials Science

Link

https://pubs.acs.org/doi/pdf/10.1021/la0488811

Reference48 articles.

1. Formation of Polyion Complex Micelles in an Aqueous Milieu from a Pair of Oppositely-Charged Block Copolymers with Poly(ethylene glycol) Segments

2. Spontaneous Formation of Polyion Complex Micelles with Narrow Distribution from Antisense Oligonucleotide and Cationic Block Copolymer in Physiological Saline

3. Water-Soluble Polyion Complex Associates of DNA and Poly(ethylene glycol)−Poly(l-lysine) Block Copolymer

4. Chain Length Recognition: Core-Shell Supramolecular Assembly from Oppositely Charged Block Copolymers

5. Block copolymer micelles for drug delivery: design, characterization and biological significance

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