| Literature DB >> 28350158 |
Ding Qu1,2, Lixiang Wang1, Meng Liu3, Shiyang Shen3, Teng Li3, Yuping Liu1,2, Mengmeng Huang1,2, Congyan Liu1,2, Yan Chen1,2, Ran Mo3.
Abstract
The aim of this study is to demonstrate the enhanced therapeutic efficacy of anticancer drugs on drug-resistant breast cancer using multicomponent microemulsions (ECG-MEs) as an oral delivery system. The etoposide-loaded ECG-MEs were composed of coix seed oil and ginsenoside Rh2 (G-Rh2), both of which possess not only the synergistic antitumor effect with etoposide, but also have excipient-like properties. Orally administrated ECG-MEs were demonstrated to be able to accumulate at the tumor site following crossing the intestines as intact vehicles into the blood circulation. The spatiotemporal controlled release characteristics of ECG-MEs brought about the efficient P-gp inhibition by the initially released G-Rh2 and the increased intracellular accumulation of the sequentially released etoposide. The combination antitumor activity of etoposide, G-Rh2 and coix seed oil using ECG-MEs was verified on the xenograft drug-resistant breast tumor mouse models. In addition, the safety evaluation studies indicated that treatment with ECG-MEs did not cause any significant toxicity in vivo. These findings suggest that ECG-MEs as an oral formulation may offer a promising strategy to treat the drug-resistant breast cancer.Entities:
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Year: 2017 PMID: 28350158 DOI: 10.1021/acs.biomac.7b00011
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988