Tissue Engineering And Nanotheranostics

(Steven Felgate) #1
b2815 Tissue Engineering and Nanotheranostics “9.61x6.69”

208 Tissue Engineering and Nanotheranostics


In this chapter, we consider a new method for attracting nanopar­


ticles to cancer cells. As difficult as that may seem, the idea is relatively


simple; cancer cells are known to have greater electromagnetic (EM)


fields than normal cells.3–12 These enhanced EM fields are then targets


for charged nanoparticles.


There are currently three traditional methods for treating cancer:


(1) Excision (via surgery); (2) Radiation (focused and repeated); and


(3) Chemotherapy (repeated and varied). Clinically, excision has the


best outcome if all of the malignant cells are removed. Radiation can


also be effective if all the malignant cells are destroyed; but the side


effects of radiation can be harmful: Normal cells may also be dam­


aged. Finally, thermotherapy is often a last resort or is used in combi­


nation with surgery and radiation. It too can be effective, but often


all of the cancer cells are not destroyed. Since cancer tumors grow


erratically and usually without sufficient oxygen and nutrients, the


tumor recruits blood vessels which expand and also become cancer­


ous, and with erratic growth.^11 With this vascular anomaly, the treat­


ing chemicals often do not reach all of the malignant cells.


Nevertheless, the tumor is usually shrunk, but over time it recurs, and


the recurring cells are usually more resistant to the treating chemicals.


But if that were not bad enough, the side effects on normal cells are


well known and often devastating.


If we can get nanoparticles to go inside the cancer cells, the


particles can be used for accurate imaging of the tumor and more


importantly, for killing its cells outright either by toxic deposit, by


vibration via external stimulation, or by heating, or also via external


stimulation.


The balance of the chapter is divided into six parts with the


following part providing some preliminary background informa­


tion about cell geometry. This is followed by a more detailed


description of centriole development and activity within the cell.


The next part provides a general description of bionano technology


which is then followed by proposed alternatives to traditional


nanoparticle therapy. The final part is a discussion with concluding


remarks.

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