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 showing iron oxide particles inside a liposome "bubble". (MIT) 
			 
 
			A team of MIT scientists 
			has constructed a type of heat-sensitive, magnetic nanoparticle that 
			can deliver chemical stimulants deep into brain tissues and release 
			them on demand, providing a new means to remotely modulate the 
			behaviors of test subjects. 
 
			Due to their biocompatibility, ability to 
			entrap a variety of small and large molecules, and versatility to 
			adopt a wide range of physicochemical and biological properties, liposomes are a popular carrier in biomedical science, capable of 
			delivering anything from plasmid DNA for gene editing, to cytotoxic 
			chemo-agents in cancer therapy. 
 They are not only a good contrast agent in Magnetic Resonance Imaging (MRI) scans, but also a perfect vehicle to induce magnetic hyperthermia - a technique extensively used in oncology treatment. 
 In a typical procedure, a colloid preparation made of nanoscale iron oxide compounds is injected directly to the vein that feed a tumor. 
 
			The colloidal particles get heated up upon 
			exposure to an alternating high-frequency magnetic field, which 
			enables them to "bake" and eventually kill off cancerous tissues 
			within the tumor. 
 
			DBS, which 
			involves placing stimulating electrodes deep inside a subject's 
			brain, is effective in treating neurodegenerative disorders such as 
			Parkinson’s disease and essential tremor.  
 
			They utilized a so-called
			
			
			magnetogenetic 
			approach - essentially deploying blood-brain barrier (BBB)-crossing MNPs to the targeted brain region and using the thermal energy 
			generated by magnetic hyperthermia to release chemical stimulants 
			encapsulated inside these lipid bubbles. 
 
			About 20 seconds later, 
			when the liposomal particles reached a temperature of 42º celsius (107.6° F), the entrapped drug molecules were 
			seen escaping from the thermally sensitive MNP. 
 Check out this video below from Nanoprobes Inc.: 
 
 
 
			 
 
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