期刊
NANO LETTERS
卷 11, 期 3, 页码 1395-1400出版社
AMER CHEMICAL SOC
DOI: 10.1021/nl200494t
关键词
Iron oxide; nanogel; nanoparticles; triggered drug release; on-demand; superparamagnetism
类别
资金
- NIH [GM073626, F32GM096546]
- Natural Sciences and Engineering Research Council of Canada
- NRSA
- MICINN, Spain
Drug delivery devices based on nanocomposite membranes containing thermoresponsive nanogels and superparamagnetic nanoparticles have been demonstrated to provide reversible, on-off drug release upon application (and removal) of an oscillating magnetic field. We show that the dose of drug delivered across the membrane can be tuned by engineering the phase transition temperature of the nanogel, the loading density of nanogels in the membrane, and the membrane thickness, allowing for on-state delivery of model drugs over at least 2 orders of magnitude (0.1-10 mu g/h). The zero-order kinetics of drug release across the membranes permit drug doses from a specific device to be tuned according to the duration of the magnetic field. Drugs over a broad range of molecular weights (500-40000 Da) can be delivered by the same membrane device. Membrane-to-membrane and cycle-to-cycle reproducibility is demonstrated, suggesting the general utility of these membranes for drug delivery.
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