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Usb4000 vis nir

Manufactured by OceanOptics
Sourced in United States

The USB4000-VIS-NIR is a compact, high-performance spectrometer designed for a wide range of applications. It features a linear CCD-array detector that can measure light wavelengths from 350 to 1000 nanometers. The spectrometer connects to a computer via a USB interface, allowing for easy integration and data acquisition.

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5 protocols using usb4000 vis nir

1

Colorimetric Analysis of Sticky Traps

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Diffuse reflectance spectrophotometry, which measures the light reflected by objects as a function of wavelength, has been widely employed to evaluate the color of biological and artificial pigments [46 (link)]. For the colored sticky traps, their spectral reflectance (without the acetate and the glue) was determined by a visible-infrared spectrophotometer (USB4000-VIS-NIR, Ocean Optics, Orlando, FL) with an optical resolution of 1.5 nm (full width at half maximum). Even though our spectrometer provided readings down to 350nm the readings between 350 and 375nm were noisy and not reliable, therefore the reliable range of 375 to 1000nm was considered for this work (Fig 2). The illumination of sticky traps was performed with a tungsten-halogen light source (LS-1, Ocean Insight, Orlando, FL). Both the illumination and the reflected light were provided and collected respectively using a fiber-optic reflection probe (R200-7-VIS-NIR, Ocean Optics, Orlando, FL). Measurements were performed using a 1s integration time. The raw reflectance spectra were corrected to eliminate the dark current and normalized with the spectrum obtained from the light source reflected on a Teflon white standard reference [47 (link)].
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2

Spectral Transmission Measurement of Apples

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In order to capture the spectral intensities of the transmittance through an apple, an acquisition system was configured with a laptop computer, spectrometer (USB4000-VIS-NIR, Ocean Optics, Orlando, FL, USA), the fixture for transmittance measurement, two types of light sources (i.e., the developed and TH lamp) as shown in Figure 2d,e. In terms of optical layout, the light source was located at the equatorial level of an apple, where the VIS/NIR radiation passes through it. At the underneath of the apple, the measurement fixture was placed with an optical probe with a collimator lens, which is connected to an optical fiber. In terms of its optical pathway, the transmitted light from the left side of an apple is measured at the optical probe in the right side, which is connected to USB4000-VIS-NIR spectrometer with an optical slit width of approximately 200 µm.
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3

Butterfly Wing Reflectance and SiO2 Replica Analysis

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The reflectance spectroscopy of butterfly Trogonoptera brookiana wings and the SiO2 negative replica were measured using a miniature fiber optic spectrometer (Ocean Optics USB4000-VIS-NIR) equipped with a halogen tungsten lamp source (Ocean Optics LS-1-LL). The spot size of the incident beam was ~2 mm, and the wavelength of the reflectance spectroscopy varied in the range of 400–900 nm. In addition, the element types and content analysis of the surface of the SiO2 negative replica were characterized by virtue of the energy dispersive spectroscopy (EDS, OXFORD X-MaxN 150) on the SEM.
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4

Tissue Phantom Characterization and Anomaly Detection

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To characterize the performance of the system, a homogeneous tissue phantom was made by diluting 20% Intralipid in a water tank. The diluted solution was 1% in concentration. The true value of reduced scattering coefficient (μs′) at this concentration was around 8.9 cm−1. A Mie calculator was used to estimate the theoretical value of the reduced scattering coefficient of the Intralipid solution. Ink solution was added into the diluted Intralipid solution to control its absorption coefficient (μa). A spectrometer (USB4000-VIS-NIR, Ocean Optics) was used to quantify the true value of the absorption coefficient. For homogeneous phantom experiments, an ink concentration of 0.01 ml/l was used. The value of the absorption coefficient for this concentration was 0.08 cm−1.
A cylindrical bead of diameter 0.5 cm and length 0.5 cm was embedded in the tissue phantom as an absorbing inhomogeneity. Two separate sets of experiments were carried out. In the first set we used a high absorption coefficient (1.64 cm−1) bead and in the second set, we used a bead with a low absorption coefficient (0.64 cm−1). The reduced scattering coefficient for both beads was 8.9 cm−1.
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5

Optical Clearing of Porcine Vaginal Wall

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A spectrometer (USB 4000-VIS-NIR, Ocean Optics, Dunedin, FL) (Figure 1C) quantified change in the reflection spectrum of porcine vaginal wall as a function of OCA application time. A fiber optic Y cable (RP21, Thorlabs, Newton, NJ) was used to connect light source (MI-150, Edmund Optics, Barrington NJ), and spectrometer. The fiber tip was in direct contact with the sample and reflectance data was collected using proprietary software (Spectra Suite, Ocean Optics). The baseline spectrum from native tissue at 0 min with that of optically cleared tissue. Percentage change in reflection spectrum due to OCA was calculated and collected every 30 s for 30 min.
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