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We present a nanosecond Q-switched Erbium-doped fiber (EDF) laser system operating at 1600 nm with a tunable repetition rate from 100 kHz to 1 MHz. A compact fiber coupled, acousto-optic modulator-based EDF ring cavity was used to generate a nanosecond seed laser at 1600 nm, and a double-cladding EDF based power amplifier was applied to achieve the maximum average power of 250 mW. In addition, 12 ns laser pulses with the maximum pulse energy of 2.4 μJ were obtained at 100 kHz. Furthermore, the Stokes shift by Raman scattering over a 25 km long fiber was measured, indicating that the laser can be potentially used to generate the high repetition rate pulses at the 1.7 μm region. Finally, we detected the photoacoustic signal from a human hair at 200 kHz repetition rate with a pulse energy of 1.2 μJ, which demonstrates that a Q-switched Er-doped fiber laser can be a promising light source for the high speed functional photoacoustic imaging.

We have developed laser-diode-based optical-resolution photoacoustic microscopy (LD-OR-PAM) of superficial microvasculature which has the desirable properties of being compact, low-cost, and label-free. A 300-mW visible pulsed laser diode was operated at a 405 ± 5 nm wavelength with a pulse energy as low as 52 nJ. By using a 3.6 MHz ultrasound transducer, the system was tested on carbon fibers with a lateral resolution of 0.95 µm and an SNR of 38 dB. The subcutaneous microvasculature on a mouse back was imaged without an exogenous contrast agent which demonstrates the potential of the proposed prototype for skin chromophores. Our eventual goal is to offer a practical and affordable multi-wavelength functional LD-OR-PAM instrument suitable for clinical applications.

Non-contact laser ultrasonic technique has been increasingly implemented for non-destructive inspections in harsh environments, high-temperature fields, and components having complex geometries. However, the poor signal-to-noise ratio and low amplitude of laser generated ultrasonic signals under a thermoelastic regime severely restrict its applications. Here, a sensitivity-enhanced all-optical probe was proposed for laser ultrasonic non-destructive testing. It consists of an optical sensor and an ellipsoidal acoustic cavity, where an optical sensor is placed at one focus of the cavity, and the detection point is set at another focus. The ultrasound signals are focused through the cavity and detected by the optical sensor. Side-by-side comparison experiments were carried out, and the results show that the probe can improve the signal amplitude by about 7.8 times compared to using a traditional optical sensor alone. The probe can make laser ultrasound detect defects with lower laser energy, which is of great significance to improve the efficiency of non-contact defect detection. [ABSTRACT FROM AUTHOR]

A photoacoustic microscope system based on virtual instrument development environment is presented, including ultrasonic sensor, digital oscilloscope, laser diode, personal calculation and other hardware platforms. and developed supporting software and image reconstruction algorithms. In the subcutaneous angiography experiment, the distribution characteristics of the ear blood vessels in mouse were completely reproduced perfectly, and the spatial resolution of the system can reach 14um. The system and method can potentially to develop into a non-invasive biological tissue structure and functional imaging technique.

Background/Aims: Islet beta cells (β-cells) are unique cells that play a critical role in glucose homeostasis by secreting insulin in response to increased glucose levels. Voltage-gated ion channels in β-cells, such as K+ and Ca2+ channels, contribute to insulin secretion. The response of voltage-gated Na+ channels (VGSCs) in β-cells to the changes in glucose levels remains unknown. This work aims to determine the role of extracellular glucose on the regulation of VGSC. Methods: The effect of glucose on VGSC currents (INa) was investigated in insulin-secreting β-cell line (INS-1) cells of rats using whole-cell patch clamp techniques, and the effects of glucose on insulin content and cell viability were determined using Enzyme-Linked Immunosorbent Assay (ELISA) and Methylthiazolyldiphenyl-tetrazolium Bromide (MTT) assay methods respectively. Results: Our results show that extracellular glucose application can inhibit the peak of INa in a concentration-dependent manner. Glucose concentration of 18 mM reduced the amplitude of INa, suppressed the INa of steady-state activation, shifted the steady-state inactivation curves of INa to negative potentials, and prolonged the time course of INa recovery from inactivation. Glucose also enhanced the activity-dependent attenuation of INa and reduced the fraction of activated channels. Furthermore, 18 mM glucose or low concentration of tetrodotoxin (TTX, a VGSC-specific blocker) partially inhibited the activity of VGSC and also improved insulin synthesis. Conclusion: These results revealed that extracellular glucose application enhances the insulin synthesis in INS-1 cells and the mechanism through the partial inhibition on INa channel is involved. Our results innovatively suggest that VGSC plays a vital role in modulating glucose homeostasis. [ABSTRACT FROM AUTHOR]