Page 136 - Bio Engineering Approaches to Cancer Diagnosis and Treatment
P. 136

134    CHAPTER 6  Laser-assisted cancer treatment





                                            E local  = E inc i ,  +  ∑ E j  = E inc i ,  +  ∑ A P ,  (6.17)
                                                                      ij
                                                                        j
                                                                    = j 1
                                                        = j 1
 Elocal=Einc, i+∑j=1i≠jEj=Einc, i+                      ≠ ij       ≠ ij
 ∑j=1i≠jAijPj,
 Aij                     where A  is the interaction matrix between all the dipoles in the particles. The scat-
                                ij
                         tering efficiency is:
                                                      k
                                              Q sca  =  2   |  E ( r) ˆ | 2             (6.18)
                                                                 ′ ⋅rdS.
                                                             sca
                                                     2
 2
 Qsca=kπr Ei ∫dS|Esca(r)′⋅rˆ| dS.                  πrE i  ∫ dS
 2
 2
                            Fourier transform and DDSCAT are the applicable methods to solve Eq. (6.18).
                         6.2  Photothermal therapy
                         Photothermal therapy (PTT) refers to using photothermal agents to selectively destroy
                         cancer cells by converting optical energy into heat. When photothermal agents expose
                         to light, the electrons transfer from the ground state to the excited state. Then, the
                         excited electron suddenly relaxes through nonradiative decay channels which leads
                         to increasing the kinetic energy and subsequently raising the temperature around the
                         targeted tissue. This heat is applied to destroy cancer cells. Several kinds of the pho-
                         toabsorbing agent have been used in PTT including natural [5] or synthetic chromo-
                         phores [6], noble metals [7], and carbon-based nanostructures [8]. In comparison to
                         synthesize chromophores such as naphthalocyanines and indocyanine green, natural
                         chromophores suffer from very low absorption cross-section. However, synthetic dye
                         molecules exhibit photobleaching during laser irradiation. There has been a tremen-
                         dous effort to develop nanoparticles for PTT.
                            The noble metals are considered a great deal of attention due to their four to
                         five times higher cross-section absorption compare to the synthetic chromophores.
                         Recently, gold nanoshells (GNSs), gold nanocages (GNCs), gold nanorods (GNRs),
                         gold nanostars (GNSTs), carbon nanotubes, and graphene oxide (GO) have been
                         considered as versatile nanoparticles for PTT on account of their strong absorption in
                         near-infrared (NIR) region, high stability, and acceptable biocompatibility. Fig. 6.1 is
                         shown these nanoparticles which is further described in the following section.

                         6.2.1  Gold nanoshells
                         GNSs compose of a dielectric core surrounded by a thin layer of gold. The surface
                         plasmon resonance (SPR) of GNSs is related to the plasmon difference between the
                         inner and outer shells. By changing the ratio of core radius to shell thickness, SPR
                         wavelength is tuned from visible to NIR [9]. The typical method to fabricate GNSs
                         is seed-mediated growth which composed of two steps—gold nanoparticle is first
                         attached to the dielectric core and then growth under the specific condition to form a
                         shell. The main studies of using GNSs for PTT are summarized in Table 6.1. GNSs,
                         with the trade name of AuroShell is currently being examined for clinical study [10].
                         When AuroShell injects intravenously in a patient, will accumulate in tumors due
   131   132   133   134   135   136   137   138   139   140   141