Abstract

BackgroundPorous silicon particles (PSiPs) have been used extensively as drug delivery systems, loaded with chemical species for disease treatment. It is well known from silicon producers that silicon is characterized by a low reduction potential, which in the case of PSiPs promotes explosive oxidation reactions with energy yields exceeding that of trinitrotoluene (TNT). The functionalization of the silica layer with sugars prevents its solubilization, while further functionalization with an appropriate antibody enables increased bioaccumulation inside selected cells.ResultsWe present here an immunotherapy approach for potential cancer treatment. Our platform comprises the use of engineered silicon particles conjugated with a selective antibody. The conceptual advantage of our system is that after reaction, the particles are degraded into soluble and excretable biocomponents.ConclusionsIn our study, we demonstrate in particular, specific targeting and destruction of cancer cells in vitro. The fact that the LD50 value of PSiPs-HER-2 for tumor cells was 15-fold lower than the LD50 value for control cells demonstrates very high in vitro specificity. This is the first important step on a long road towards the design and development of novel chemotherapeutic agents against cancer in general, and breast cancer in particular.

Highlights

  • Introduction to Nanomedicine and NanobioengineeringNew York: Wiley; 2012. 2

  • Silicon is characterized by a reduction potential [26] of −1.697 eV to yield silicates or −0.91 eV to yield silica, which is dissolved as silicates in the presence of water

  • In summary, we present here an immunotherapy approach for potential cancer treatment

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Summary

Introduction

Introduction to Nanomedicine and NanobioengineeringNew York: Wiley; 2012. 2. 6. Hong C, Lee J, Son M, Hong SS, Lee C: In-vivo cancer cell destruction using porous silicon nanoparticles. 8. Xiao L, Gu L, Howell SB, Sailor MJ: Porous silicon nanoparticle photosensitizers for singlet oxygen and their phototoxicity against cancer cells. Porous silicon particles (PSiPs) have been used extensively as drug delivery systems, loaded with chemical species for disease treatment. It is well known from silicon producers that silicon is characterized by a low reduction potential, which in the case of PSiPs promotes explosive oxidation reactions with energy yields exceeding that of trinitrotoluene (TNT). Particles have shown great potential [1] for drug delivery [2,3,4] and cancer treatment [5,6,7,8]. By coating with a compact monolayer of an organic molecule, dissolution can be retarded or even prevented

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