Novel ABA block copolymers: preparation, temperature sensitivity, and drug release
Document Type
Article
Publication Date
12-20-2022
Abstract
A new PEGylated macroiniferter was prepared based on the polycondensation reaction of polyethylene oxide (PEO), methylene diphenyl diisocyanate (MDI), and 1,1,2,2-tetraphenyl-1,2-ethanediol (TPED). The macroiniferter consists of PEO end groups and readily reacts with acrylamides (such as N-isopropylacrylamide, NIPAM) and forms ABA block copolymers (PEO-PNIPAM-PEO). This approach of making amphiphilic ABA block copolymers is robust, versatile, and useful, particularly for the development of polymers for biomedical applications. The resulting amphiphilic PEO-PNIPAM-PEO block copolymers are also temperature sensitive, and their phase transition temperatures are close to human body temperature and therefore they have been applied as drug carriers for cancer treatment. Two PEO-PNIPAM-PEO polymers with different molecular weights were prepared and selected to make temperature-sensitive micelles. As a result of the biocompatibility of these micelles, cell viability tests proved that these micelles have low toxicity toward cancer cells. The resultant polymer micelles were then used as drug carriers to deliver the hydrophobic anticancer drug doxorubicin (DOX), and the results showed that they exhibit significantly higher cumulative drug release efficiency at higher temperatures. Moreover, after loading DOX into the micelles, cellular uptake experiments showed easy uptake and cell viability tests showed that DOX-loaded micelles possess a better therapeutic effect than free DOX at the same dose.
Identifier
85145352011 (Scopus)
Publication Title
Rsc Advances
External Full Text Location
https://doi.org/10.1039/d2ra05831f
e-ISSN
20462069
First Page
129
Last Page
139
Issue
1
Volume
13
Grant
1R21GM140438-01
Fund Ref
National Science Foundation
Recommended Citation
Dou, Jie; Yu, Shupei; Reddy, Ojasvita; and Zhang, Yuanwei, "Novel ABA block copolymers: preparation, temperature sensitivity, and drug release" (2022). Faculty Publications. 2402.
https://digitalcommons.njit.edu/fac_pubs/2402