Plasma Damage Control: From Biomolecules to Cells and Skin.

The antibacterial and cell-proliferative character of atmospheric pressure plasma jets (APPJs) helps in the healing process of chronic wounds. However, control of the plasma-biological target interface remains an open issue. High vacuum ultraviolet/ultraviolet (VUV/UV) radiation and RONS flux from plasma may cause damage of a treated tissue; therefore, controlled interaction is essential. VUV/UV emission from argon APPJs and radiation control with aerosol injection in plasma effluent is the focus of this research. The aerosol effect on radiation is studied by a fluorescent target capable of resolving the plasma oxidation footprint. In addition, DNA damage is evaluated by plasmid DNA radiation assay and cell proliferation assay to assess safety aspects of the plasma jet, the effect of VUV/UV radiation, and its control with aerosol injection. Inevitable emission of VUV/UV radiation from plasmas during treatment is demonstrated in this work. Plasma has no antiproliferative effect on fibroblasts in short treatments (t < 60 s), while long exposure has a cytotoxic effect, resulting in decreased cell survival. Radiation has no effect on cell survival in the medium due to absorption. However, a strong cytotoxic effect on the attached fibroblasts without the medium is apparent. VUV/UV radiation contributes 70% of the integral plasma effect in induction of single- and double-strand DNA breaks and cytotoxicity of the attached cells without the medium. Survival of the attached cells increases by 10% when aerosol is introduced between plasma and the cells. Injection of aerosol in the plasma effluent can help to control the plasma-cell/tissue interaction. Aerosol droplets in the effluent partially absorb UV emission from the plasma, limiting photon flux in the direction of the biological target. Herein, cold and safe plasma-aerosol treatment and a safe operational mode of treatment are demonstrated in a murine model.

Demonstration of up-conversion fluorescence from Ar clusters in intense free-electron-laser fields.

Extreme ultraviolet (EUV) fluorescence emitted from Ar clusters irradiated by intense EUV free electron laser (FEL) pulses has been investigated. The EUV fluorescence spectra display rich structure at wavelengths shorter than the incident FEL wavelength of 51 nm. The results suggest that multiply-charged ions are produced following the ion-electron recombination processes which occur in the nanoplasma created by multi-photon excitation during the intense EUV-FEL pulses.

Spectroscopic and thermodynamic features of conical bubble luminescence.

The influence on luminescence from conical bubble collapse (CBL) with varying Ar gas content while perturbing the liquid 1,2-Propanediol (PD) has been investigated. The temporal, spatial, and spectral features were analysed with regards to the dynamics of collapse and liquid degradation. Sulphuric acid and sodium chloride were added to disturb the liquid. The following three cases were studied: PD/Ar, (I), (PD + H(2)SO(4))/Ar, (II), and (PD + H(2)SO(4) + NaCl)/Ar, (III). The intensities of those cases decrease as III > II > I. Temporally, single and multiple light emissions were found to occur. The pulse shape exhibited a large variety of profiles with a main maximum and up to two local maxima around the main maximum. These local maxima resembled those generated by laser cavitation. Spatially, no radial symmetry was detected in the light emissions. Spectrally, the Swan, CH and CN lines were observed at low volumes of gas and driving pressure. The ·OH radical and OH-Ar bands, as well as the Na and K lines, consistently appeared superimposed on an underlying continuum that almost disappeared in (III). The Na line was observed with two satellite diffuse bands representing Na-Ar complexes in (I) and (II), whereas in (III), only the line of sodium could be seen. Weak and diffuse emission lines from the Ar atom in the near-IR region were observed in (I) and (II). The proposed mechanism of bright CBL was based on the energy transfer from electron-excited homolytic cleavage products to the chromophore molecules generated during the collapse-rebound time line (~8200 K and ~1 ms of collapse time from model), which had accumulated inside the liquid and remained on the walls of cavity during the repetition of the collapse. A general mechanism for the bright CBL is broached.

Enhanced Kα output of Ar and Kr using size optimized cluster target irradiated by high-contrast laser pulses.

We observed that increasing the clusters size and laser pulse contrast can enhance the X-ray flux emitted by femtosecond-laser-driven-cluster plasma. By focusing a high contrast laser (10(-10)) on large argon clusters, high flux Kα-like X-rays (around 2.96 keV) is generated with a total flux of 2.5 × 10(11) photons/J in 4π and a conversion efficiency of 1.2 × 10-4. In the case of large Kr clusters, the best total flux for L-shell X-rays is 5.3 × 1011 photons/J with a conversion efficiency of 1.3 × 10-4 and, for the Kα X-ray (12.7 keV), it is 8 × 10(8) photons/J with a conversion efficiency of 1.6 × 10-6. Using this X-ray source, a single-shot high-performance X-ray imaging is demonstrated.

Sonolysis of an oxalic acid solution under xenon lamp irradiation.

The photosonolysis of oxalic acid was carried out in an Ar atmosphere. The detectable products of sonolysis were CO(2), CO, H(2), and H(2)O(2). The yield of CO(2) was higher than that for the sum of sonolysis and photolysis reactions. Namely, a synergistic effect was observed during simultaneous irradiations of 200 kHz ultrasound and Xe lamp. The degradation of oxalic acid was promoted by active species such as H(2)O(2) produced from water by sonolysis. An oxalic acid-H(2)O(2) complex is likely to be present in the solution, but could not be detected. The effects of not only the photo-irradiation but also the thermal or incident energy during Xe lamp illumination were also considered.

Supercontinuum generation and pulse compression from gas filamentation of femtosecond laser pulses with different durations.

Self-compression and spectral supercontinuum (SC) generated by filamentation of femtosecond laser pulses with duration from 45 fs down to 6 fs in argon gas have been numerically investigated. A 45-fs pulse can be self-compressed into a few-cycle pulse with duration of 12 fs at the post-filamentation region. By properly employing a high-pass filter to select the broadening high-frequency spectra which are almost in phase, the pulse can be further shortened to about 7 fs. By contrast, a 6-fs pulse cannot be further self-compressed into a shorter pulse by filamentation although it can generate much broader SC extending from 200 nm to 1300 nm. It is also found that a separate and strong SC in the ultraviolet (UV) region extending from 220 nm to 300 nm and peaked at about 255 nm can be generated at proper propagation distances, which corresponds to a pulse with duration of about 5 fs.

Terahertz pulse radiation from argon clusters.

The characteristics of THz pulse radiation from argon clusters irradiated with intense femtosecond laser pulses have been investigated. The average power of the THz pulses radiated from argon clusters is approximately 40 times greater than that from argon gas. The enhancement of the THz radiation originates from large laser absorption by the clusters. The polarization state and the angular distribution of the power of the THz pulses show no dependence on laser polarization, which suggests that the radiation originates from laser-induced charge separation along the laser propagation direction.

Dual-color co-filamentation in Argon.

We investigate both experimentally and theoretically the mechanisms driving the co-filamentation of two ultrashort laser pulses at 800 and 400 nm in Argon. The cross-Kerr lens and cross-phase modulation between the two filaments of different colors bridging both the continuum spectra and the plasma channels induced by the individual pulses. This dual-color filamentation also results in the simultaneous generation of two few-cycle pulses at both 800 and 400 nm, providing a potential way to generate attosecond pulses.

Chlorine-39 in rainfall at a temperate latitude (40 degrees N).

Rainwater samples were collected and measured for the radioactivity to confirm the presence of Chlorine-39 (T1/2=56.2 min) formed by the interaction of cosmic-ray slow negative muons, mu- with Argon-40 in the lower atmosphere. The presence of 39Cl was confirmed by estimating the half-life of a radionuclide present in the rainwater ranging from 58 to 63 min and averaging 60.4 min. The disintegration rate of this radionuclide varied from 2.1 to 2.7 Bq L(-1) (125-160 dpm/L) of rainwater and averaged 2.3 Bq L(-1) (140 dpm/L) of rainwater in Thessaloniki (40 degrees 38'N, 22 degrees 58'E), Northern Greece. This concentration is indicative of mid or temperate latitudes. This is clearly less than that reported in the literature, 1.7 Bq L(-1) (100 dpm/L) of rainwater, for a southern latitude 31 degrees 54'N, 34 degrees 49'E (Rehovot, Israel), due to the latitudinal effect of cosmic radiation.

Towards non-sequential double ionization of Ne and Ar using a femtosecond laser oscillator.

We report on first proof-of-principles results on non-sequential double ionization of argon and neon achieved by using a newly developed long-cavity Ti:sapphire femtosecond oscillator with a pulse duration of 45 fs and a repetition of 6.2 MHz combined with a dedicated reaction microscope. Under optimized experimental conditions, peak intensities larger than 2.310(14) W/cm(2) have been achieved. Ion momentum distributions were recorded for both rare gases and show significantly different features for single as well as for double ionization. For single ionization of neon a spike of zero-momentum electrons is found when decreasing the laser intensity towards the lowest ionization rate we can measure which is attributed to a non-resonant ionization channel. As to double ionization, the longitudinal momentum distribution for Ne(2+) displays a clear double-hump structure whereas this feature is found to be smoothened out with a maximum at zero momentum for Ar(2+).

Velocity map imaging of ion-molecule reactive scattering: the Ar(+)+ N(2) charge transfer reaction.

We present a velocity map imaging spectrometer for the study of crossed-beam reactive collisions between ions and neutrals at (sub-)electronvolt collision energies. The charge transfer reaction of Ar(+) with N(2) is studied at 0.6, 0.8 and 2.5 eV relative collision energies. Energy and angular distributions are measured for the reaction product N. The differential cross section, as analyzed with a Monte Carlo reconstruction algorithm, shows significant large angle scattering for lower collision energies in qualitative agreement with previous experiments. Significant vibrational excitation of N(+)(2) is also observed. This theoretically still unexplained feature indicates the presence of a low energy scattering resonance.

CF4 plasma treatment of poly(dimethylsiloxane): effect of fillers and its application to high-aspect-ratio UV embossing.

Surface modification of poly(dimethylsiloxane) (PDMS) was carried out via CF4 plasma treatment. The test PDMS used contains significant amounts of quartz and silica fillers, while the control material is the same PDMS with quartz removed by centrifugation. Fluorination accompanied with roughening was produced on both PDMS surfaces. With short plasma times (15 min or less), a macromolecular fluorocarbon layer was formed on the PDMS surfaces because of the dominant fluorination, leading to significant increase in F concentration, decrease of surface energy, and some roughening. With intermediate plasma times (15-30 min), dynamic balance between fluorination and ablation was achieved, leading to a plateau of the surface roughness, fluorine content, and [F-Si]/[F-C] ratio. At our longest investigated plasma time of 45 min, the plasma ablated the fluorinated covering layer on the PDMS surfaces, leading to significant increase in roughness and [F-Si]/[F-C] ratio and decrease of surface F concentration. The effect of additional quartz in the test PDMS on surface F concentration, [F-Si]/[F-C] ratio, and roughness was dramatic only when ablation was significant (i.e., 45 min). The obtained Teflon-like surface displays long-term stability as opposed to hydrophobic recovery of other plasma-treated PDMS surfaces to increase hydrophilicity. On the basis of the optimized plasma treatment time of 15 min, a microstructured PDMS mold was plasma treated and successfully used for multiple high-aspect-ratio (about 8) UV embossing of nonpolar polypropylene glycol diacrylate (PPGDA) resin.

Spectroscopic characterization of two different microwave (2.45 GHz) induced argon plasmas at atmospheric pressure.

A surface-wave-sustained discharge created by using a surfatron device in a tube open to the atmosphere can be used to maintain a microwave (2.45 GHz) plasma at atmospheric pressure at powers of less than 300 W. The TIA (Torche a Injection Axiale) is a device also producing a plasma that, moreover, permits us to work at high power (higher than 200 W and up to 1000 W). A study of the departure from the thermodynamic equilibrium existing in the argon plasmas created by both devices has been done by using optical emission spectroscopy techniques in order to characterize them and to evaluate their possible advantages when they are used for applied purposes.

Dose verification of single shot gamma knife applications using VIPAR polymer gel and MRI.

This work describes an experimental procedure with potential to assess the overall accuracy associated with gamma knife clinical applications, from patient imaging and dosimetry planning to patient positioning and dose delivery using the automated positioning system of a Leksell Gamma Knife model C. The VIPAR polymer gel-MRI dosimetry method is employed due to its inherent three-dimensional feature and linear dose response over the range of gamma knife applications. Different polymer gel vials were irradiated with single shot gamma knife treatment plans using each of the four available collimator helmets to deliver a maximum dose of 30 Gy. Percentage relative dose results are presented not only in the form of one-dimensional profiles but also planar isocontours and isosurfaces in three dimensions. Experimental results are compared with corresponding Gammaplan treatment planning system calculations as well as acceptance test radiochromic film measurements. A good agreement, within the experimental uncertainty, is observed between measured and expected dose distributions. This experimental uncertainty is of the order of one imaging pixel in the MRI gel readout session (<1 mm) and allows for the verification of single shot gamma knife applications in terms of acceptance specifications for precision in beam alignment and accuracy. Averaging net R(2) results in the dose plateau of the 4 mm and 18 mm collimator irradiated gel vials, which were MR scanned in the same session, provides a crude estimate of the 4 mm output factor which agrees within errors with the default value of 0.870.

Characterisation of radionuclides formed by high-energy neutron irradiation.

The physicochemical properties of radionuclides suspended in the air are important parameters in order to evaluate internal doses due to the inhalation of the airborne radionuclides and to develop the air-monitoring system in high-energy proton accelerator facilities. This study focuses on the property of radioactive airborne chlorine (38Cl and 39Cl) and sulphur (38S) produced in Ar gas by irradiation with high-energy neutrons. As a result of the irradiation of a mixture of Ar gas and dry air, 38Cl and 39Cl existed as non-acidic gas and 38S was present as acidic gas. Furthermore, it has been found that in the high-energy neutron irradiation of aerosol containing Ar gas, the higher the amount of radioactive aerosols, the lower will be the amount of radioactive acidic gas.

Evaluation of the performance of VIPAR polymer gels using a variety of x-ray and electron beams.

The aim of this investigation was the evaluation of the usefulness of N-vinyl pyrrolidone argon (VIPAR) polymer gel dosimetry for relative dose measurements using the majority of types and energies of radiation beams used in clinical practice. For this reason, VIPAR polymer gels were irradiated with the following beams: 6 and 23 MV photons (maximum dose: 15 Gy) and 6, 9, 12, 15, 18 and 21 MeV electrons (90% dose: 15 Gy). Using 6 MV x-rays, a linear gel dose response was verified for doses up to 20 Gy. Assuming linearity of response for the rest of the photon and electron beams used in this study, percentage depth dose measurements were derived. For all beams used and the range of relative doses studied, a satisfying agreement was observed between percentage depth dose measurements performed using the VIPAR gel-MRI method and an ion chamber, validating the assumption that a linear gel dose response holds for all photon and electron beams studied. VIPAR gels, therefore, can be used for relative dose distribution measurements using photons or electrons of any typical energy used in external radiotherapy applications. It is also demonstrated that two-dimensional dose distribution measurements through an irradiated (9 MeV electrons, 3 cm x 3 cm cone) VIPAR gel volume can be easily obtained.

Particle size analysis of radioactive aerosols formed by irradiation of argon using 65 MeV quasi-monoenergetic neutrons.

The size distributions of 38Cl and 39Cl aerosols formed from the irradiation of argon gas containing di-octyl phthalate (DOP) aerosols by 65 MeV quasi-monoenergetic neutrons were measured to study the formation mechanism of radioactive aerosols in high-energy radiation fields. Both the number size distribution and the activity-weighted size distribution were measured using an electrical low-pressure impactor. It was found that the 35Cl and 39Cl aerosols are formed by attachment of the radioactive atoms generated by the neutron-induced reaction to the DOP aerosol particles.

Corona discharge of Titan's troposphere.

The atmosphere of Titan is constantly bombarded by galactic cosmic rays and Saturnian magnetospheric electrons causing the formation of free electrons and primary ions, which are then stabilized by ion cluster formation and charging of aerosols. These charged particles accumulate in drops in cloud regions of the troposphere. Their abundance can substantially increase by friction, fragmentation or collisions during convective activity. Charge separation occurs with help of convection and gravitational settling leading to development of electric fields within the cloud and between the cloud and the ground. Neutralization of these charge particles leads to corona discharges which are characterized by low current densities. These electric discharges could induce a number of chemical reactions in the troposphere and hence it is of interest to explore such effects. We have therefore, experimentally studied the corona discharge of a simulated Titan's atmosphere (10% methane and 2% argon in nitrogen) at 500 Torr and 298 K by GC-FTIR-MS techniques. The main products have been identified as hydrocarbons (ethane, ethyne, ethene, propane, propene + propyne, cyclopropane, butane, 2-methylpropane, 2-methylpropene, n-butene, 2-butene, 2,2-dimethylpropane, 2-methylbutane, 2-methylbutene, n-pentane, 2,2-dimethylbutane, 2-methylpentane, 3-methylpentane, n-hexane, 2,2-dimethylhexane, 2,2-dimethylpentane, 2,2,3-trimethylbutane, 2,3-dimethylpentane and n-heptane), nitriles (hydrogen cyanide, cyanogen, ethanenitrile, propanenitrile, 2-methylpropanenitrile and butanenitrile) and an uncharacterized film deposit. We present their trends of formation as a function of discharge time in an ample interval and have derived their initial yields of formation. These results clearly demonstrate that a complex organic chemistry can be initiated by corona processes in the lower atmosphere. Although photochemistry and charged particle chemistry occurring in the stratosphere can account for many of the observed hydrocarbon species in Titan, the predicted abundance of ethene is to low by a factor of 10 to 40. While some ethene will be produced by charged-particle chemistry, its production by corona processes and subsequent diffusion into the stratosphere appears to be an adequate source. Because little UV penetrates to the lower atmosphere to destroy the molecules formed there, the corona-produced species may be long-lived and contribute significantly to the composition of the lower atmosphere and surface.

Utilizaçäo do laser de argônio em anastomose do intestino delgado: trabalho experimental em ratos / Use of argon laser in anastomosis of the intestine small: experimental work in rats

Os autores apresentam um trabalho preliminar da utilizaçäo do laser de Argônio de forma experimental, na anastomose de intestino delgado de ratos, submetidos a enterotomia total a bisturi. Os resultados macro e microscópicos iniciais obtidos, demonstram a possibilidade técnica do evento, possibilitando a continuidade do estudo experimental quanto à avaliaçäo do colágeno e resistência tecidual, bem como avaliaêäo qualitativa comparando-se à sutura convencional