In this letter, we report a process for room-temperature assembly of patterned and periodic structures of carbon nanotubes ͑CNTs͒. Well-defined patterns with less than a 10-m linewidth and variable thickness were readily deposited. The CNTs show long-range in-plane orientation ordering and adhere strongly to the substrates. The self-assembled macroscopic structures emit electrons under applied electrical field with the emission characteristics comparable to those from the high-temperature or/and low-resolution deposition processes. This room-temperature self-assembly method can be utilized for assembly and integration of nanostructured materials for a variety of devices, including the field-emission displays.

Speed and temporal resolution are critical for tomographic imaging of objects in rapid motion. Current x-ray scanners record images sequentially in the time domain. The serial approach limits their performance and demands increasingly high x-ray peak power and gantry speed. We have developed a multipixel carbon nanotube based field emission x-ray source that produces spatially and temporally modulated radiations. Using this device we show the feasibility of multiplexing radiography that enables simultaneous collection of multiple projection images using frequency multiplexing. A drastic increase of the speed and reduction of the x-ray peak power are achieved without compromising the imaging quality.

We report a dynamic radiography system with a carbon nanotube based field-emission microfocus x-ray source. The system can readily generate x-ray radiation with continuous variation of temporal resolution as short as nanoseconds. Its potential applications for dynamic x-ray imaging are demonstrated. The performance characteristics of this compact and versatile system are promising for noninvasive imaging in biomedical research and industrial inspection.

We have developed a compact microbeam radiation therapy device using carbon nanotube cathodes to create a linear array of narrow focal line segments on a tungsten anode and a custom collimator assembly to select a slice of the resulting wedge-shaped radiation pattern. Effective focal line width was measured to be 131 lm, resulting in a microbeam width of $300 lm. The instantaneous dose rate was projected to be 2 Gy/s at full-power. Peak to valley dose ratio was measured to be >17 when a 1.4 mm microbeam separation was employed. Finally, multiple microbeams were delivered to a mouse with beam paths verified through histology. V C 2013 AIP Publishing LLC.[http://dx.doi.org/10.1063/1.4826587] More than half of cancer patients in North America rely on radiation therapy (RT) as part of their treatment plan.

The mechanisms by which fasting decreases liver insulin-like growth factor I (IGF-I) messenger RNA (mRNA) abundance have not been defined completely. In the present study, we have examined the effects of fasting in rats on hepatic IGF-I gene transcription, IGF-I pre-mRNA splicing, and cytoplasmic IGF-I mRNA stability. Using the in vitro nuclear run-on transcription technique, we observed that fasting did not change IGF-I gene transcription activity [76 +/- 32 densitometric units (DU) for fasted vs. 58 +/- 23 DU for control-fed rats; P = 0.1], whereas IGF-binding protein-1 (IGFBP-1) gene transcription, a positive control, was increased more than 2-fold (729 +/- 157 DU for fasted vs. 261 +/- 56 DU for control-fed rats; P < 0.05). This implies that fasting-induced reduction of liver IGF-I mRNA is due to events other than a decreased rate of IGF-I gene transcription. By measuring nonspliced (pre-mRNA) and spliced IGF-I transcripts in liver nuclear RNA using ribonuclease protection assays, we found that IGF-I pre-mRNA was increased in fasted rats (measured as the percentage of beta-actin: 34.0 +/- 5.5% for fasted vs. 8.1 +/- 3.8% for control-fed rats; P < 0.01), whereas spliced IGF-I transcript remained unchanged (measured as the percentage of beta-actin: 60.9 +/- 9.2% for fasted vs. 79.0 +/- 6.2% for control-fed rats; P = 0.75). We then compared this pattern of splicing to IGF-I pre-mRNA splicing in hypophysectomized rats subjected to GH stimulation and to IGFBP-1 pre-mRNA splicing in the same fasting experiment. One hour after GH injection, we observed a coordinate increase in both nonspliced and spliced IGF-I transcripts in liver nuclei of hypophysectomized rats. Fasting increased both IGFBP-1 pre-mRNA and spliced transcript. Taken together, these results indicate that the increase in IGF-I pre-mRNA in liver nuclei during fasting is caused by delayed pre-mRNA splicing, rather than increased IGF-I gene transcription. To examine the possible effect of fasting on hepatic IGF-I mRNA stability, we used an in vitro model of nutrient deprivation (fewer amino acids in culture medium) of rat hepatocyte primary culture. Each of the three major IGF-I mRNA species exhibited a shortened half-life in the amino acid-deprived media. The 7.5-kb IGF-I mRNA, however, was degraded faster than the two smaller IGF-I mRNA species. This may indicate that fasting decreases the stability of liver IGF-I mRNA in vivo. In summary, these results suggest that fasting regulates hepatic IGF-I gene expression mainly at the posttranscriptional level by delaying IGF-I pre-mRNA splicing, which attenuates mature IGF-I mRNA generation, and by accelerating the rate of degradation of IGF-I mRNA in cytoplasm.