| Literature DB >> 29205852 |
Chao Zhang1, Zunfeng Liu2, Ying Zheng3, Yadi Geng1, Chao Han1, Yamin Shi1, Hongbin Sun1, Can Zhang1, Yijun Chen1, Luyong Zhang1, Qinglong Guo1, Lei Yang1, Xiang Zhou3, Lingyi Kong1.
Abstract
Mitochondria-mediated apoptosis (MMA) is a preferential option for cancer therapy due to the presence of cell-suicide factors in mitochondria, however, low permeability of mitochondria is a bottleneck for targeting drug delivery. In this paper, glycyrrhetinic acid (GA), a natural product from Glycyrrhiza glabra, is found to be a novel mitochondria targeting ligand, which can improve mitochondrial permeability and enhance the drug uptake of mitochondria. GA-functionalized graphene oxide (GO) is prepared and used as an effective carrier for targeted delivery of doxorubicin into mitochondria. The detailed in vitro and in vivo mechanism study shows that GA-functionalized GO causes a decrease in mitochondrial membrane potential and activates the MMA pathway. The GA-functionalized drug delivery system demonstrates highly improved apoptosis induction ability and anticancer efficacy compared to the non-GA-functionalized nanocarrier delivery system. The GA-functionalized nanocarrier also shows low toxicity, suggesting that it can be a useful tool for drug delivery.Entities:
Keywords: cancer therapy; delivery; glycyrrhetinic acid; mitochondria targeting; mitochondria-mediated apoptosis
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Year: 2017 PMID: 29205852 DOI: 10.1002/smll.201703306
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281