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通过含氧化铁纳米粒子的脂质体膜的磁场驱动触发脂质体释放。

Triggered release from liposomes through magnetic actuation of iron oxide nanoparticle containing membranes.

机构信息

Laboratory for Surface Science and Technology, ETH Zurich, Wolfgang-Pauli-Strasse 10, CH-8093 Zürich, Switzerland.

出版信息

Nano Lett. 2011 Apr 13;11(4):1664-70. doi: 10.1021/nl2001499. Epub 2011 Feb 25.

DOI:10.1021/nl2001499
PMID:21351741
Abstract

The ideal nanoscale drug delivery vehicle allows control over the released dose in space and time. We demonstrate that this can be achieved by stealth liposomes comprising self-assembled superparamagnetic iron oxide nanoparticles (NPs) individually stabilized with palmityl-nitroDOPA incorporated in the lipid membrane. Alternating magnetic fields were used to control timing and dose of repeatedly released cargo from such vesicles by locally heating the membrane, which changed its permeability without major effects on the environment.

摘要

理想的纳米级药物输送载体可以控制释放剂量在空间和时间上的分布。我们证明,通过由自组装超顺磁性氧化铁纳米粒子(NPs)组成的隐形脂质体可以实现这一点,这些 NPs 分别由棕榈酰-硝基 DOPA 稳定,该物质整合在脂质膜中。通过局部加热改变膜的通透性,可以在不对外界产生重大影响的情况下,利用交变磁场来控制从这些囊泡中反复释放的货物的时间和剂量。

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