材料科学
纳米技术
生物相容性材料
剩磁
转染
磁性纳米粒子
纳米颗粒
磁铁
钕磁铁
铁磁性
磁化
生物医学工程
细胞培养
磁场
医学
生物
物理
量子力学
遗传学
作者
Vincent Mauricio Kadiri,Claudio Bussi,Andrew W. Holle,Kwanghyo Son,Hyunah Kwon,Gisela Schütz,Maximiliano G. Gutiérrez,Peer Fischer
标识
DOI:10.1002/adma.202001114
摘要
Abstract The application of nanoparticles for drug or gene delivery promises benefits in the form of single‐cell‐specific therapeutic and diagnostic capabilities. Many methods of cell transfection rely on unspecific means to increase the transport of genetic material into cells. Targeted transport is in principle possible with magnetically propelled micromotors, which allow responsive nanoscale actuation and delivery. However, many commonly used magnetic materials (e.g., Ni and Co) are not biocompatible, possess weak magnetic remanence (Fe 3 O 4 ), or cannot be implemented in nanofabrication schemes (NdFeB). Here, it is demonstrated that co‐depositing iron (Fe) and platinum (Pt) followed by one single annealing step, without the need for solution processing, yields ferromagnetic FePt nanomotors that are noncytotoxic, biocompatible, and possess a remanence and magnetization that rival those of permanent NdFeB micromagnets. Active cell targeting and magnetic transfection of lung carcinoma cells are demonstrated using gradient‐free rotating millitesla fields to drive the FePt nanopropellers. The carcinoma cells express enhanced green fluorescent protein after internalization and cell viability is unaffected by the presence of the FePt nanopropellers. The results establish FePt, prepared in the L1 0 phase, as a promising magnetic material for biomedical applications with superior magnetic performance, especially for micro‐ and nanodevices.
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