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35 protocols using labview 2015

1

Printed Silver Nanoparticle Circuits

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We used Kapton polyimide film as an adhesive substrate to attach on a certain level of free-form surface and silver nanoparticles (576, 832, <100-nm diameter, Sigma-Aldrich, Saint Louis, MO, USA) as printing materials. The printing process is occurred by mechanical movements of substrate driven by multi-axis stage (SGSP20, Sigma Koki, Japan) with a velocity of 0.2 mms−1 which is controlled by LabVIEW 2015 and NI USB 6009 modules (National Instrument, Austin, TX, USA). The AgNPs erupted from a nozzle with an inner diameter of 150 µm (Taeha Co., Korea). After a wiring and soldering process using silver paste (conductive paste, 735,825, Sigma-Aldrich, Saint Louis, MO, USA) at the tip of printed line pattern, UV curable adhesives (UV-3300, Skycares Co., Gimpo, Korea) are wrapped for electrical insulation and mechanical protection from external stimulation.
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2

Single-cell electrophysiology of cultured neurons

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For single-cell electrophysiology recording, cultured neurons were incubated in Tyrode’s buffer containing 20 μM Gabazine, 10 μM NBQX and 25 μM APV. The electrophysiology experiments were performed at room temperature. Borosilicate glass electrodes (Sutter) were pulled to a tip resistance of 2.5–5 MΩ. The glass electrode was filled with internal solution containing 145 mM potassium gluconate, 5 mM MgCl2, 10 mM HEPES, and 4 mM Na2-ATP (pH 7.2, with KOH). The glass electrode’s position was adjusted by a Sutter MP285 micro-manipulator. Membrane potentials were recorded under whole-cell current clamp under I = 0 mode (Axopatch 200B, Axon Instruments). Recorded membrane potential data were filtered with a 5 kHz internal Bessel filter in the amplified and digitized with a National Instruments PCIe-6353 data acquisition 1067 (DAQ) board. The microscope (Nikon Ti-E), the camera (Hamamatsu ORCA-Flash 4.0 v2) and electrophysiology recording system were controlled with a customized software written in LabVIEW 2015 (National Instruments), and the data were extracted and analyzed with a home-made script written in MATLAB R2018b (MathWorks).
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3

Multimodal Imaging Protocol for Tissue Analysis

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Processed OCM volumes consisted of 4096(z)×500(x)×500(y) pixels and the fluorescence images comprised 500(x)×500(y)  pixels . The field of view was 200×200  μm2 . Data were acquired using a custom made Labview program (LabView 2015, Version 15.0, 64-bit, National Instruments). The OCM data were processed following the steps described by Lichtenegger et al.,7 (link) and en-face projections were generated by averaging intensity over various depths. Fiji was used to generate composition images of FI and OCM results.68 (link)
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4

Participant Preparation for Functional MRI

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Participants lay supine in the bore, with their head stabilized by noise-canceling headphones and foam padding. Images were presented on an MR-compatible 30″ LCD screen (Invivo, Gainesville, FL) that was placed at the head of the scanner and reflected with a rearward facing single reflection mirror box that was affixed to the top of the head-coil. Behavioral responses were collected utilizing an MR-compatible 4-button response box (Lumina LP-400, Cedrus Corporation, San Pedro, CA) placed at participant midline, just below the chest in order to minimize participant movement throughout the experiment. The response pad consisted of a keypad with four horizontally arranged buttons; participants were instructed to only press button one with their index finger to respond (or two buttons to move the scale bar to the left or right for the ranking emotion task) using their dominant (right) hand. To ensure the button box did not move throughout the experiment, it was affixed to the participant’s wrist via a Velcro strap. Stimulus presentation and data recording were accomplished using a dedicated PC running custom LabVIEW software (LabVIEW 2015, National Instruments, Austin, TX).
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5

Two-Photon Microscope Operating Protocol

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The two-photon microscope was operated using ScanImage v5.3 (Vidrio Technologies, LLC) software and a custom written software written in LabView 2015 (National Instruments). The code is available upon request to authors.
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6

Large-scale OCT Imaging via Motorized Stage

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Large FoV images were acquired with the JM-OCT prototype in combination with a motorized translation stage (MLS203-1, Thorlabs) moving in x and y direction. The stage was integrated into the sample arm and was able to scan large field-of-views up to several square centimeter. The maximal range of the stage was 11.0 cm × 7.5 cm. A custom-made LabView (LabView 2015, Version 15.0, 64-bit, National Instruments) program controlled the movement of the translation stage [59 (link)]. The OCT data were acquired with an overlap, in the lateral direction, of 5% and after post-processing the volumes were stitched together using the Pairwise stitching plugin of Fiji [60 (link)].
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7

Cerebrovascular Autoregulation Assessment

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All stored data were exported from ICM+ software to plain text files and imported in MATLAB (Release 2019b, The MathWorks, Inc., Natick, MA, USA). NIRS data was first visually inspected, and artifacts were removed (details on the applied methodology can be found in Supplementary Figure S1). Then, the data was stored in ten-minute data segments per patient and imported into a custom made LabVIEW program (LabVIEW 2015, National Instruments, Austin, TX, USA) calculating the CA-estimates (Section 2.4.1) as used in Elting et al. [9 (link)]. Sufficiently slow ABP oscillations are required for a reliable CA assessment [10 (link)]. The amount of slow ABP and resulting slow oxyHb and deoxyHb oscillations were quantified by the Power Spectral Density (PSD).
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8

Robotic Exoskeleton Design and Functionality

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The robotic exoskeleton used in this study (Figure 1) consisted of active hip and knee joints and passive ankle joints. Active joints were powered by electrical motors with a gear ratio of 76 : 1, with assistive torque delivered to the wearer's joints in the sagittal plane. Active joints adopted a series elastic actuation mechanism [21 (link), 22 (link)], enabling accurate control of the interaction torque between robot and human joints. Dynamic ankle-foot orthosis was used as the passive ankle joint to support the weight of the exoskeleton and to provide a sufficient degree of freedom in the wearer's ankle joint. Foot pressure under the metatarsal joint and the heel was measured using silicon tubes and air pressure sensors to estimate the ground reaction force [23 (link)]. All algorithms required to operate the exoskeleton, such as sensor signal processing and the control algorithm, were implemented using the embedded control board (sbrio 9651, National Instruments, TX, USA) and software (LabVIEW 2015, National Instruments, TX, USA). The embedded control board and battery, enclosed in a backpack, enabled the exoskeleton to be fully mobile. The total weight of the robotic exoskeleton was 13 kg.
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9

Multimodal Imaging of Tissue Microstructure

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Fluorescence images consisted of 500 (x) × 500 (y) pixels and the processed OCM data sets comprised 500 (x) × 500 (y) × 4096 (z) pixels, each covering the same 200 × 200 µm2 lateral FOV. OCM volumes and FL intensities were acquired in 8.3 seconds using custom software (LabVIEW 2015, Version 15.0, 64-bit, National Instruments, Austin, TX, USA). Data were processed as previously described by Lichtenegger et al. [30 (link)]. After image acquisition, surface flattening was performed and attenuation maps were computed from OCM reflectivity data [65 (link),66 (link)]. Sub-volumes consisting of 100 B-scans were chosen in a manually defined region of interest and average attenuation coefficients were calculated. Respective fluorescence intensities on the tissue surface were quantified and normalized linearly between zero and one, with the upper and lower values defined as the minimum and maximum, respectively, of all data sets. For visualization purposes, Fiji [67 (link)] was used to generate averaged en-face projections and composition images.
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10

Micro-LED Mechanical Strain Evaluation

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In order to evaluate the stable functionality of the micro-LED array under mechanical strain, cycling experiments were performed. The devices were mounted on a custom-built uniaxial stretcher and stretched to 1.15 of their initial length for 100k cycles (1 stretching cycle to maximal strain per second). The voltage was monitored continuously while applying i = 5 mA (Keithley 2400 SourceMeter). The stretcher and the measurement equipment were controlled and synchronized using custom-made software based on LabVIEW 2015 (National Instruments).
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