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Attenuated total reflectance accessory

Manufactured by PerkinElmer
Sourced in United States

The Attenuated Total Reflectance (ATR) accessory is a specialized laboratory equipment used in spectroscopic analysis. It enables the direct measurement of solid or liquid samples by creating an evanescent wave that interacts with the sample's surface, allowing for quick and convenient sample analysis without the need for extensive sample preparation.

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5 protocols using attenuated total reflectance accessory

1

Mid-Infrared Spectroscopy Characterization

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The samples produced were characterized by mid-infrared (MIR) spectroscopy. Spectra (n = 3) were acquired using a Frontier spectrometer (PerkinElmer, Beaconsfield, UK) equipped with an attenuated total reflectance (ATR) accessory (PerkinElmer, Beaconsfield, UK) equipped with a pressure arm to control the applied force and reduce sample-to-sample variability. The spectrometer had a deuterated triglycine sulfate (DTGS) detector and a mid-infrared light source. The samples were placed directly on the crystal of the ATR accessory, and each spectrum was the resultant of 32 accumulations at a resolution of 8 cm−1 over the range 4000–600 cm−1. The background spectrum was acquired for the empty crystal following cleaning.
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2

Characterizing MCE-Alginate Interactions

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The interaction of MCE and sodium alginate in MCB was observed by using FT-IR with an attenuated total reflectance (ATR) accessory (Perkin Elmer, Norwalk, CT, USA). The FT-IR analysis was conducted according to the previous study [11 (link)]. The sample was compressed between two ART diamond crystals. Spectra of the samples were recorded in the transmission mode at a resolution of ±4 cm−1 and 32 scans, covering a wavenumber range of 400–4000 cm−1.
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3

Reflectance Micro-FTIR Analysis of Direct Placement and CAD/CAM RBC Samples

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The particles from all direct placement and CAD/CAM RBC sampleswere washed with ultra-high quality (UHQ) water, and left to dry at room temperature for 8 h, prior to deposition on a stainless-steel flat sample holder for infrared micro-analysis. Reflectance micro-FTIR spectra were taken on a Perkin Elmer Spotlight 400 FT-IR Imaging System (Perkin Elmer, Waltham, MA, USA). Micro Fourier Transform Infrared (FTIR) spectra were collected over the 4000 cm−1 to 700 cm−1 wavenumber range, in reflectance mode, using a liquid nitrogen cooled Mercury–Cadmium–Telluride (MCT) array detector, at a resolution of 8 cm−1 and an aperture of 20 μm. Sixteen scans were taken for each pixel in the infrared maps, where each pixel corresponded to a square of 20 µm per side. A Kramer–Kronig transformation was not needed, as the resulting spectra did not present specular reflectance distortions.
Samples were also analysed on a Perkin Elmer Frontier Fourier Transform Infrared (FTIR) spectrometer (Perkin Elmer, Waltham, MA, USA), using a Perkin Elmer Attenuated Total Reflectance (ATR) accessory, consisting of a diamond crystal at a fixed angle of 45°. One-hundred spectra were collected over the 4000 cm−1 to 650 cm−1 wavenumber range, at a resolution of 4 cm−1.
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4

FTIR Spectral Analysis of Samples

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FTIR spectra were obtained in a FT-IR/NIR Frontier Spectrometer equipped with an Attenuated Total Reflectance accessory (PerkinElmer, USA) at a scan range of 4000 to 600 cm−1 and spectral resolution of 4 cm−1. Spectrum software version 10.03.07 was used to determine the peak positions.
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5

Characterization of MUF Cube Morphology

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The morphology of MUF cubes was observed by scanning electron microscopy (SEM). Images were obtained using a JEOL JSM 6300 microscope at the Central Service for Research Support of the University of Córdoba. Chromatographic analysis was carried out on a Shimadzu (Kyoto, Japan) HPLC system coupled to a SPD-M20A Diode Array Detector (DAD). The column used for the separation was a Hypersil ODS (250 × 4.6 mm, 5 µm particle size) from Thermo Fisher Scientific (Waltham, MA, USA), kept at 25 °C in a CTO 10AS column oven. Samples were injected using a Rheodyne injector with a sample loop of 20 µL volume. The mobile phase consisted of water (A) and acetonitrile (B), containing 0.1% (v/v) formic acid. The analytes were separated following a gradient elution program from 55% to 80% B in 30 min and then to 85% in 5 min. The total chromatogram time was 35 min. Mobile phase was delivered using a LC20AD pump, at a flow rate of 0.8 mL min−1. The detector was set at a wavelength range of 200–360 nm. Data acquisition and processing were carried out using a LC-solution software version 1.21. FTIR spectra were recorded on a Spectrum Two FTIR using an attenuated total reflectance accessory (PerkinElmer, Cambridge, MA, USA). Approximate contact angle measurements were carried out by analyzing various photographs of water droplets on MUF cubes using the Corel Draw X6 software.
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