Based on the following information I need a simple conclusion that encounters that:

What contributions will this research have in the field?

Overall strengths

Overall weaknesses

What are next steps for research

Steps could include how to correct weaknesses/ gaps

“Lung cancer is very prominent in todays' society”

“Targeting cancerous tumors benefits surgical and therapeutic efforts”

“Current range of addressable biomarkers is satisfactory”

“Current methods are functional but leave much to be desired”

“Clinical Trials in nanoparticle and heavy metal targeting agents to come”

Describe some of the different ways that RADIOTHERAPY could be functionalized to accumulate in ORAL CANCER tissue. Would it be more beneficial to perform active or passive targeting? If you were to perform active targeting, what are 3 different tissue biomarkers you would try to target, and why? What sorts of targeting molecules would you put on the surface of Gold nanoparticles ? What are your most important considerations when picking targeting molecules (size, charge, affinity, etc)? How do you expect this active targeting to change your overall nanoparticle accumulation in your tissue? If you were to perform passive targeting, what physical properties of your nanoparticle would you optimize, and why? How do you expect this passive targeting to change your overall nanoparticle accumulation in your tissue?

pick one of these nanoparticles gold particle,silver particle ,magnetic nanoparticle, nanosponges. to answer these questions. Describe some of the different ways this nanoparticle could be functionalized to accumulate in cancer tissue?would it be more beneficial to perform active or passive targeting? if you were to perform active targeting, what are 3 different tissue biomarkers you would try to target and why? what sorts of targeting molecules would you put on the surface of your nanoparticles? what are your most important consideration when picking targeting molecules such as size,charge, affinity?how do you expect this active targeting to change your overall nanoparticle accumulation in your tissue? if you were to perform passive targeting, what passive targeting of your nanoparticle would you optimize and why? how do you expect this passive targeting to change your overall nanoparticle in your tissue?

Pick a nanoparticle you described in a previous about breast cancer. Describe some of the different ways this nanoparticle could be functionalized to accumulate in your diseased tissue of interest. Would it be more beneficial to perform active or passive targeting? If you were to perform active targeting, what are 3 different tissue biomarkers you would try to target, and why? What sorts of targeting molecules would you put on the surface of your nanoparticle? What are your most important considerations when picking targeting molecules (size, charge, affinity, etc)? How do you expect this active targeting to change your overall nanoparticle accumulation in your tissue? If you were to perform passive targeting, what physical properties of your nanoparticle would you optimize, and why? How do you expect this passive targeting to change your overall nanoparticle accumulation in your tissue?
my topic is talking about breast cancer