| Literature DB >> 23613425 |
Hyun-Ouk Kim1, Eunjung Kim, Yonghee An, Jihye Choi, Eunji Jang, Eun Bi Choi, Aastha Kukreja, Myeong-Hoon Kim, Byunghoon Kang, Dong-Joo Kim, Jin-Suck Suh, Yong-Min Huh, Seungjoo Haam.
Abstract
Combined cancer treatment via co-delivery of siRNAs and an anticancer drug can be a promising strategy due to the synergistic effect of simultaneously minimizing gene/drug administration. In this study, Bcl-xL siRNA and doxorubicin (DOX) are encapsulated into designed methoxy-poly(ethylene glycol)-block-poly(D,L-lactic acid) (mPEG-b-PLA) block copolymer polymersomes (PSomes). A study of the cytotoxicity of Bcl-xL siRNA and DOX co-encapsulated PSomes (CPSomes) shows more inhibited proliferation of MKN-45 and MKN-28 human gastric cancer cell lines than only gene- and drug-loaded ones. Consequently, these results demonstrate that co-delivery of genes and drugs using PSomes results in a synergistic efficacy and indicates the potential of PSomes as efficient nanocarriers for combined cancer therapy.Entities:
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Year: 2013 PMID: 23613425 DOI: 10.1002/mabi.201200448
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979