Ceramic nanoparticles . Describe some of thedifferent ways this nanoparticle could be functionalized toaccumulate in type 1 diabetes tissue . Would it bemore beneficial to perform active or passive targeting? If you wereto perform active targeting, what are 3 different tissue biomarkersyou would try to target, and why? What sorts of targeting moleculeswould you put on the surface of your nanoparticle? What are yourmost important considerations when picking targeting molecules(size, charge, affinity, etc)? How do you expect this activetargeting to change your overall nanoparticle accumulation in yourtissue? If you were to perform passive targeting, what physicalproperties of your nanoparticle would you optimize, and why? How doyou expect this passive targeting to change your overallnanoparticle accumulation in your tissue?
Ceramic nanoparticles . Describe some of thedifferent ways this nanoparticle could be functionalized toaccumulate in type 1 diabetes tissue . Would it bemore beneficial to perform active or passive targeting? If you wereto perform active targeting, what are 3 different tissue biomarkersyou would try to target, and why? What sorts of targeting moleculeswould you put on the surface of your nanoparticle? What are yourmost important considerations when picking targeting molecules(size, charge, affinity, etc)? How do you expect this activetargeting to change your overall nanoparticle accumulation in yourtissue? If you were to perform passive targeting, what physicalproperties of your nanoparticle would you optimize, and why? How doyou expect this passive targeting to change your overallnanoparticle accumulation in your tissue?
