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Investigation of Tumor Optical Properties after Laser-Induced Photothermal Treatment

This study investigates the change in tumor optical properties after laser-induced photothermal treatment using gold nanoparticles. The results show a decrease in absorption and scattering properties of the tumor and surrounding tissues, leading to increased penetration depth of laser radiation into the tumor.

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Investigation of Tumor Optical Properties after Laser-Induced Photothermal Treatment

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  1. INVESTIGATION OF CHANGE OF TUMOR OPTICAL PROPERTIES AFTER LASER-INDUCED PLASMON-RESONANT PHOTOTHERMAL TREATMENT OF TRANSPLANTED TUMORS IN RATS Vadim D. Genin1, Elina A. Genina1,2, Alla B. Bucharskaya3, Valery V. Tuchin1,2, Nikolay G. Khlebtsov4, Alexey N. Bashkatov1,2 1 – Saratov State University (National ResearchUniversity), Russia 2 – Tomsk State University (National Research University), Russia 3 – Saratov State Medical University, Russia 4 – Institute of Biochemistry and Physiology of Plants and Microorganisms RAS, Russia

  2. After the invention of laser in 1960 the study of low-intensive laser radiation action on biological tissues began. The thermal effect of laser radiation on the tissues was founded. That effect was accompanied by the hyperthermia, which became a therapy method of cancer tumors treatment at the temperature 41-450С. Today the metal nanoparticles are used for the increase of the laser radiation selectivity. Plasmon-resonant nanoparticles are capable to excite local surface plasmon resonance in visible and NIR ranges of spectrum. That leads to increased absorption and/or scattering of probing radiation. Such nanoparticles are capable for generating a thermal energy, which makes it possible to reduce the dose of laser radiation The Motivation of the Study

  3. The Objective of the Study Investigation of change of tumor optical properties of the rat tumor doped by gold nanoparticles after laser-induced plasmon-resonant photothermal treatment

  4. MATERIALSAND METHODS

  5. The Gold Nanoparticles The TEM image of gold nanoparticles and their size distribution The gold nanoparticles were synthesized in Laboratory of Nanoscale Biosensors of Institute of Biochemistry and Physiology of Plants and Microorganisms RAS. For aggregation preventing, the nanoparticles were functionalized by thiolated polyethylene glycol (molecular weight 5000 Da, Nektar, USA). The size of nanoparticles were: length 41±8 nm, diameter 10±2 nm. Concentration in suspension was: 400 pg/mL (optical density 20 on the wavelength 800 nm)

  6. The Laboratory Animals Outbred albino male rats with the weight 160-200 g were used. To obtain the model tumors the rats were implanted by 0.5 mL of 25% suspension of alveolar kidney cancer cells. The experimental model of rat cancer was reproduced by transplantation of tumor cell suspension of cancer, obtained from the bank of tumor strains of Russian Cancer Research Center n.a. N.N. Blokhin. When the tumor reached the diameter 3.0±0.3 cm2 the animals were randomly divided into two groups: control and experimental ones. Before the experiment, the animals were anesthetized with Zoletil 50(Virbac, France). The dose was 0.5 mg/kg. An hour before the experiment the animals were injected by the suspension of gold nanoparticles from 3 points with injection speed 0.1 mL/min. This method of injection led to nanoparticles accumulation and retention in the tumor

  7. The Equipment IR vizualizer IRI4010 (IRYSYS, UK) Diode laser LS-2-N-808-10000 (808 nm, 2.3 W/cm2, the area of the irradiation spot ~0.5 см2, time of radiation 7.5 min) (Laser Systems, Ltd., St. Petersburg, Russia) Spectrophotometer UV-3600 (Shimadzu, Japan) with integrating sphere LISR-3100 (Shimadzu, Japan). Wavelength range 350-2200 nm

  8. The Skin Temperature Kinetics t, min Temperature kinetics of skin surface above the tumor During the irradiating the temperature on the skin surface was registered with IR vizualizer every 0.5 min.

  9. The Analysis of the Temperature Kinetics The temperature kinetics can be described well by two-exponential dependence: where A1 and A2 are the empirical constants, τ1и τ2 are the characteristic times of tissue heating processes, y0 is the maximum signal level. The characteristic times are τ1 = 0.24±0.05 min andτ2 = 4.07±0.6 min, y0reaches 85.8°С

  10. RESULTS

  11. The Absorption Spectra of Tumor and Surrounding Tissues Before the nanoparticles injection and laser irradiating After the nanoparticles injection and laser irradiating

  12. The Reduced Scattering Coefficient Spectra of Tumor and Surrounding Tissues Before the nanoparticles injection and laser irradiating After the nanoparticles injection and laser irradiating

  13. The Scattering Coefficient Spectra of Tumor and Surrounding Tissues Before the nanoparticles injection and laser irradiating After the nanoparticles injection and laser irradiating

  14. The Spectral Dependence of the Scattering Anisotropy Factor of Tumor and Surrounding Tissues Before the nanoparticles injection and laser irradiating After the nanoparticles injection and laser irradiating

  15. Summary The results of the experiment shows that after doping the tumor tissue by the plasmon resonant nanoparticles and NIR laser irradiating, there is the decreases of absorption as well as scattering properties of the tumor and surrounding tissues, which leads to the increase of the penetration depth of the laser radiation into the tumor. At the same time, it is clear that, despite the sufficiently high temperature on the surface (about 80°C), the changes in the center of the tumor are insignificant, and therefore, for better therapeutic effect, it is need either to increase the power of the incident radiation, or to increase the irradiation time, or to decrease the scattering of tissue covering the tumor.

  16. Thank you for your attention!

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