Volume 218, Issue 15 1700068
Full Paper

Dual pH-Sensitive DOX-Conjugated Cyclodextrin-Core Star Nano-Copolymer Prodrugs

Yu Hou

Yu Hou

Key Laboratory of Macromolecular Science and Technology of Shaanxi Province, Department of Applied Chemistry, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education, School of Science, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

Search for more papers by this author
Yuyang Liu

Corresponding Author

Yuyang Liu

Key Laboratory of Macromolecular Science and Technology of Shaanxi Province, Department of Applied Chemistry, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education, School of Science, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

E-mail: [email protected]Search for more papers by this author
Shuangshuang Sun

Shuangshuang Sun

Key Laboratory of Macromolecular Science and Technology of Shaanxi Province, Department of Applied Chemistry, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education, School of Science, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

Search for more papers by this author
Jianghu Liang

Jianghu Liang

Key Laboratory of Macromolecular Science and Technology of Shaanxi Province, Department of Applied Chemistry, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education, School of Science, Northwestern Polytechnical University, Xi'an, 710072 P. R. China

Search for more papers by this author
First published: 15 May 2017
Citations: 11

Abstract

Herein this study reports dual pH-sensitive doxorubicin (DOX)-conjugated β-cyclodextrin-core star copolymers with tailoring properties such as direct water-solubility and stability prior to reaching target sites. For these purposes, three kinds of novel well-defined β-cyclodextrin-core poly(2-(diethylamino)ethyl methacrylate-co-4-formylphenyl methacrylate)-b-poly(poly(ethylene glycol) methyl ether methacrylate) star copolymers (CD-star-P(DEA-co-FPMA)-b-PPEGMA, SPDFP1–3) with different poly(ethylene glycol) methyl ether methacrylate contents are designed and synthesized by atom transfer radical polymerization (ATRP) strategy. 4-Formylphenyl methacrylate is introduced into the inner arm block of the star copolymers for conjugating DOX by imine bond formation. Interestingly, the DOX-conjugated β-cyclodextrin-core star copolymers not only can directly dissolve in aqueous buffer solution of pH 7.0 to form unimolecular micelles without any aid of organic solvent, but also exhibit strong pH-dependent DOX release. At normal pH 7.4 the DOX amount released is very small, whereas at pH 5.0 DOX can be released. By selecting SPDFP2–DOX as a representative, it is found that the SPDFP2–DOX micelles show less cytotoxicity compared to carrier-free DOX and can be internalized by HeLa cells. It is expected that the exploration can provide new strategy for preparing drug delivery system.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.