Transparent solids may show strong absorption when irradiated by a high-intensity laser pulse. Such laser induced breakdown is due to the formation of a free-electron gas. We investigate theoretically the role of ionization processes in a defect-free crystal, including in our model two competing processes: strong-electricfield ionization and electron impact ionization. Free-electron heating is described in terms of electron-phononphoton collisions. Relaxation of the free electron gas occurs through electron-electron collisions and electronphonon collisions. The latter are also responsible for energy transfer from the free-electron gas to the phonon gas. We solve numerically a system of time dependent Boltzmann equations, where each considered process is included by its corresponding collision integral. Our results show formation, excitation, and relaxation of the electron gas in the conduction band. We find that strong-electric-field ionization is mainly responsible for free-electron generation. No avalanche occurs at femtosecond laser irradiation. The electron density and the internal energies of the subsystems are calculated. Critical fluences obtained using various criteria for damage threshold are in good agreement with recent experiments.

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Very high and broad Curie maxima are observed in ceramic Ba(Til-,Zr,)03 mixed crystals, which are often used for the preparation of ceramic dielectrics. The ferroelectric-toparaelectric phase transition of ceramic Ba(Til-,Zry)Os was studied using dielectric measurements, quantitative DTA, X-ray diffraction, and determination of the remanent polarization. At higher Zr concentrations, it was found that ferroelectric and paraelectric phases coexist in a wide temperature region. Up toy =0.16, the phase transition remains first order. The diffuse character is promoted by the small energy difference between the ferroelectric and paraelectric phases appearing at higher Zr content. It can be best described by a normal distribution of Curie temperatures using the phenomenological theory of Devonshire and the Newton-Raphson mathematical approximation.

In this study we evaluated the effects of intracellular compartmentalization of the ultrasmall superparamagnetic iron oxide (USPIO) ferumoxtran-10 on its proton T1 and T2 relaxivities at 1.5 and 3T. Monocytes were labeled with ferumoxtran-10 by simple incubation. Decreasing quantities of ferumoxtran-10-labeled cells (2.5x10(7)-0.3x10(7) cells/ml) and decreasing concentrations of free ferumoxtran-10 (without cells) in Ficoll solution were evaluated with 1.5 and 3T clinical magnetic resonance (MR) scanners. Pulse sequences comprised axial spin echo (SE) sequences with multiple TRs and fixed TE and SE sequences with fixed TR and increasing TEs. Signal intensity measurements were used to calculate T1 and T2 relaxation times of all samples, assuming a monoexponential signal decay. The iron content in all samples was determined by inductively coupled plasma atomic emission spectrometry and used for calculating relaxivities. Measurements at 1.5T and 3T showed higher T1 and T2 relaxivity values of free extracellular ferumoxtran-10 as opposed to intracellularly compartmentalized ferumoxtran-10, under the evaluated conditions of homogeneously dispersed contrast agents/cells in Ficoll solution and a cell density of up to 2.5x10(7) cells/ml. At 3T, differences in T1-relaxivities between intra- and extracellular USPIO were smaller, while differences in USPIO T2-relaxivities were similar compared with 1.5T. In conclusion, cellular compartmentalization of ferumoxtran-10 changes proton relaxivity.

The purpose of this study was to design, synthesize, and initially characterize a representative set of novel constructs for large-molecular radiographic/computed tomography (CT) contrast agents, intended for a primarily intravascular distribution. A new assembly of well-known and biocompatible components consists of paired, symmetrical dendritic polylysines initiated from both ends of a poly(ethylene glycol) (PEG) core, yielding an array of multiple free amino groups to which were conjugated highly soluble and stable triiodophthalamide ("triiodo") moieties. An array of six dendritic contrast agents was synthesized originally, using three different PEG cores (3, 6, 12 kDa) with t-Boc lysine-generated dendrimer "amplifiers" (from three to five generations) containing 16 to 64 amino groups for conjugation with reactive triiodo moieties. A clinically used, nonionic, small molecular CT contrast agent, iobitridol, was derivatized via a hydroxyl protection/deprotection strategy, introducing a new carboxyl group available for conjugation to the lysine amino groups of dendrimers. Final products were purified by size exclusion chromatography and characterized by NMR, UV, HPLC, and elemental analysis. Preliminary evaluations were conducted for physicochemical characterization and in vivo CT contrast enhancement in a rat model. All six iodinated PEG-core dendrimer conjugates were synthesized in good yields, with a high degree of size monodispersity, large apparent molecular weight, favored physicochemical properties. A representative compound, PEG12000-carbamate-Gen4-IOB conjugate, 27% (w%) rich in iodine, demonstrated a desirable strong and persistent intravascular enhancement with a monoexponential blood half-life of approximately 35 min assayed by dynamic CT imaging and also showed high water solubility (>550 mg/mL at 25 degrees C), large apparent molecular size (comparable to a 143-kDa protein), high hydrophilicity (butanol-water partition coefficient 0.015), and stability to autoclaving conditions. This study showed the synthetic feasibility, desired basic characteristics, and potential utility for CT contrast enhancement achieved with a new type of iodinated, large-molecular PEG-core dendritic construct. Further development of this class of macromolecular contrast agents will be required to define the optimal formulation, pharmacology, safety profile, and the full range of diagnostic applications including tumor microvascular quantitative characterization by CT imaging.