| Literature DB >> 29885900 |
Akram Assali1, Omid Akhavan2, Mohsen Adeli3, Shayan Razzazan4, Rassoul Dinarvand5, Saeid Zanganeh6, Masoud Soleimani7, Meshkat Dinarvand8, Fatemeh Atyabi9.
Abstract
Recent insights into the nanomedicine have revealed that nanoplatforms enhance the efficacy of carrier in therapeutic applications. Here, multifunctional nanoplatforms were utilized in miRNA-101 delivery and NIR thermal therapy to induce apoptosis in breast cancer cells. Au nanorods (NRs) or nanospheres (NSs) covered with graphene oxide (GO) were prepared and functionalized with polyethylene glycol as a stabilizer and poly-L-arginine (P-L-Arg) as a targeting agent. In nanoplatforms, coupling Au@GO prepared stable structures with higher NIR reactivity. P-L-Arg substantially enhanced the cellular uptake and gene retardation of stuffs coated by them. However, rod-shape nanoplatforms indicated better performance in cellular uptake and gene transfection than spherical ones. NIR thermal therapy was implemented to improve gene release and in synergy with miRNA-101 activated the apoptotic pathway and decreased the viability of breast cancer cell (<20%). Briefly, presented delivery systems are potentially efficient in distinguishing cancer cells, miRNA internalization and controlling apoptosis of cancer cells.Entities:
Keywords: Gold nanoplatform; Graphene oxide; Photothermal therapy; Poly-L-arginine; miRNA
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Year: 2018 PMID: 29885900 DOI: 10.1016/j.nano.2018.05.016
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307