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4 protocols using ldc240c

1

Laser-Powered NMR Spectroscopy Protocol

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The light source used for the experiments consisted of a 450 nm laser diode with a 1.6 W maximum output power. The optical power is decreased to the milliWatt range by using a controller that regulates the current through the diode. The current controller (Thorlabs, LDC240C) can be switched on and off to regulate the duration and intensity of the light manually. A temperature controller (Thorlabs, TED200C) is also used to ensure no variation of the output light power. A photometer PM100D (Thorlabs) was used to monitor the desired power from the light beam coming out of a 400 µm (internal diameter) optical fiber. An optical fiber (Thorlabs, FT400EMT) of 400 µm diameter is used to guide the light from the laser diode to the sample. All photo-CIDNP experiments were carried out in continuous light irradiation mode, in combination with continuous flow regime (except for the detection of 5-fluorouracile which was acquired in stopped-flow conditions). The enhancement factor experiments for Fig. 8 were acquired with a 600 µm (internal diameter, FT600EMT) optical fiber and optimal output powers were determined to obtain maximum signal (Supplementary Figs. 1014).
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2

Compact Continuous-Wave Photoacoustic Tomography

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Figure S2b shows the schematic drawing of the CW-PAT system, utilizing an inexpensive, compact, and durable laser diode (L808P1000MM, Thorlabs, maximum power: 1000 mW; wavelength: 808 nm) as the excitation source. The laser diode was installed in a laser mount (TCLDM9, Thorlabs), which was driven by a laser diode current controller (LDC240C, Thorlabs). We modulate the power of the laser diode at 1 MHz with 100% modulation depth by applying an 8.5 V square wave to the RF input of laser mount. In front of the laser diode, we used a convex lens (C230TMD-B, Thorlabs) to collimate the diode output. Similar to the pulsed PA experiment, we sealed the contrast in a tube, which was covered by a slice of 3-mm thick breast tissue. Position of the sample was adjusted to ensure that the tube phantom could generate the highest PA signal. The light intensity on the surface of chicken tissue was quantified to be 500 mW/cm2, which is within the ANSI safety limit of 808 nm (3.29 W/cm2). A 1 MHz single element transducer (E1012-SU, Mana) with a 12.7 mm diameter is co-axially placed beneath the laser beam to detect the generated PA signal, which was first amplified 80 dB by a low noise amplifier (351A-3-50-NI, Analog Modules) and then acquired by an oscilloscope (Tektronix DP3034).
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3

Laser-Powered Fiber Optic Illumination

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The low-power light source used for the experiments consisted of a laser diode (Thorlabs, L450P1600MM) emitting at 450 nm and operating at 1.6 W output power. The optical power was lowered to the milliwatt range by using a potentiometer that regulated the current through the diode, enabling the selection of the minimal current to achieve maximal signal enhancement to avoid signal distortion due to sample overheating. A photometer was used to monitor the desired power from the light beam coming out of a BFH optical fiber with 1000 μm diameter, purchased from Thorlabs (Germany). This current controller (Thorlabs, LDC 240C) could be switched on and off to regulate the duration and intensity of the light pulse either manually (continuous irradiation) or in a pulsed manner by a TTL signal directly from the spectrometer. A temperature controller (Thorlabs, TED 200C) was also used to ensure no variation in output light power of the current controller (LDC, 240C) for a certain current value [26 (link)].
The claddings of the optical fiber tip were stripped off, the main part of the fiber was masked, and the 21 mm at the tip of the fiber was sandblasted to roughen its surface, thus making it emit light over its whole range instead of just from its tip. Silicium carbide 180 was used as the abrasive material [23 (link)].
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4

Laser-based Worm Tracking and Stimulation

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On an optical table, a CCD camera (Manta G-125, Allied Vision Technologies, Newburyport, Massachusetts), a motorized microscope stage (MAX20X, Thorlabs), and a stepper motor controller (BSC102, Thorlabs) were assembled to move a 10 cm agar plate while acquiring images. Two galvanometer scanners (GVS002, Thorlabs), an analog output module (NI 9263, National Instruments), a fiber-coupled IR laser (FOL1404QQM-617-1440, Fitel), a laser diode controller (LDC240C, Thorlabs), and a temperature controller (TED350, Thorlabs) were added to steer and deliver an IR laser beam with high precision. A laboratory-developed software package in LabVIEW (National Instruments) controls all the devices, acquires images, recognizes a freely-moving worm, continuously moves the stage for tracking, and steers galvanometer scanners to deliver IR zaps to the head region of the worm. 100 ms, 50–250 mA laser zaps were used as noxious heat stimuli. After the acquisition, the images were manually labeled to calculate mean reversal durations right after the laser stimuli.
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