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Development of a robust pH-sensitive polyelectrolyte ionomer complex for anticancer nanocarriers

Authors
Lim, ChaeminYoun, Yu SeokLee, Kyung SooHoang, Ngoc HaSim, TaehoonLee, Eun SeongOh, Kyung Taek
Issue Date
2016
Publisher
DOVE MEDICAL PRESS LTD
Keywords
polyelectrolyte ionomer complex; PEG-PLA-PEI; nanomedicine; pH-sensitive; animal imaging
Citation
INTERNATIONAL JOURNAL OF NANOMEDICINE, v.11, pp 703 - 713
Pages
11
Journal Title
INTERNATIONAL JOURNAL OF NANOMEDICINE
Volume
11
Start Page
703
End Page
713
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/8655
DOI
10.2147/IJN.S99271
ISSN
1178-2013
1178-2013
Abstract
A polyelectrolyte ionomer complex ( PIC) composed of cationic and anionic polymers was developed for nanomedical applications. Here, a poly( ethylene glycol)-poly(lactic acid)poly (ethylene imine) triblock copolymer (PEG-PLA-PEI) and a poly(aspartic acid) (P[Asp]) homopolymer were synthesized. These polyelectrolytes formed stable aggregates through electrostatic interactions between the cationic PEI and the anionic P(Asp) blocks. In particular, the addition of a hydrophobic PLA and a hydrophilic PEG to triblock copolyelectrolytes provided colloidal aggregation stability by forming a tight hydrophobic core and steric hindrance on the surface of PIC, respectively. The PIC showed different particle sizes and zeta potentials depending on the ratio of cationic PEI and anionic P(Asp) blocks (C/A ratio). The doxorubicin (dox)-loaded PIC, prepared with a C/A ratio of 8, demonstrated pH-dependent behavior by the deprotonation/protonation of polyelectrolyte blocks. The drug release and the cytotoxicity of the dox-loaded PIC (C/A ratio: 8) increased under acidic conditions compared with physiological pH, due to the destabilization of the formation of the electrostatic core. In vivo animal imaging revealed that the prepared PIC accumulated at the targeted tumor site for 24 hours. Therefore, the prepared pH-sensitive PIC could have considerable potential as a nanomedicinal platform for anticancer therapy.
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