In this paper, the timing of vortex formation on the glottal jet is studied using previously published velocity measurements of flow through a scaled-up model of the human vocal folds. The relative timing of the pulsatile glottal jet and the instability vortices are acoustically important since they determine the harmonic and broadband content of the voice signal. Glottis exit jet velocity time series were extracted from time-resolved planar DPIV measurements. These measurements were acquired at four glottal flow speeds (u SS = 16.1-38 cm/s) and four glottis open times (T o = 5.67-23.7 s), providing a Reynolds number range Re = 4100-9700 and reduced vibration frequency f* = 0.01-0.06. Exit velocity waveforms showed temporal behavior on two time scales, one that correlates to the period of vibration and another characterized by short, sharp velocity peaks (which correlate to the passage of instability vortices through the glottis exit plane). The vortex formation time, estimated by computing the time difference between subsequent peaks, was shown to be not well-correlated from one vibration cycle to the next. The principal finding is that vortex formation time depends not only on cycle phase, but varies strongly with reduced frequency of vibration. In all cases, a strong high-frequency burst of vortex motion occurs near the end of the cycle, consistent with perceptual studies using synthesized speech.
This work discusses in vivo experiments that were performed to evaluate whether local or whole-body heating to 40 °C reduced interstitial fluid pressures (IFPs) and enhanced nanoparticle delivery to subcutaneous PC3 human prostate cancer xenograft tumors in mice. After heating, 0.2 mL of a previously developed nanofluid containing gold nanoparticles (10 mg Au/mL) was injected via the tail vein. The induced whole-body hyperthermia led to increases in tumor and mouse body blood perfusion rates of more than 50% and 25%, respectively, while the increases were much smaller in the local heating group. In the whole-body hyperthermia groups, the IFP reduction from the baseline at the tumor center immediately after heating was found to be statistically significant when compared to the control group. The 1 h of local heating group showed IFP reductions at the tumor center, while the IFPs increased in the periphery of the tumor. The intratumoral gold nanoparticle accumulation was quantified using inductively coupled plasma mass spectrometry (ICP-MS). Compared to the control group, 1 h or 4 h of experiencing whole-body hyperthermia resulted in an average increase of 51% or 67% in the gold deposition in tumors, respectively. In the 1 h of local heating group, the increase in the gold deposition was 34%. Our results suggest that 1 h of mild whole-body hyperthermia may be a cost-effective and readily implementable strategy for facilitating nanoparticle delivery to PC3 tumors in mice.
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