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Atr ftir spectrometer

Manufactured by PerkinElmer
Sourced in United States, United Kingdom

The ATR-FTIR spectrometer is an analytical instrument that uses Attenuated Total Reflection Fourier Transform Infrared Spectroscopy (ATR-FTIR) to analyze the molecular composition of samples. It is designed to identify and quantify various chemical compounds by measuring their unique infrared absorption spectra.

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21 protocols using atr ftir spectrometer

1

ATR-FTIR Spectroscopy of Samples

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The spectra were measured at a wavelength range of 4000-400 cm−1 with a 2 cm−1 resolution at ambient temperature (25 ± 0.5°C) using an ATR-FTIR spectrometer (PerkinElmer, Inc., USA). For each sample, 16 scans were performed, and two replicate spectra were obtained. The background air spectrum was subtracted from the spectral data. Before sample placement for analysis, the ATR element (ZnSe crystal, 45° ends) was cleaned with acetone and the results were recorded in absorbance units.
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2

Nanosheet Functional Group Analysis

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Functional groups of nanosheets and bulks were identified by a PerkinElmer ATR-FTIR spectrometer with a diamond crystal and resolution of 4 cm−1 by averaging the measurements over 16 scans. An average of 10 adjacent points from the diamond crystal detector was smoothly applied to the dried nanosheets and bulk samples.
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3

ATR-FTIR Analysis of VCL-co-HA Polymers

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The spectroscopic analysis of the monomers (VCL and HA) and polymers (p(VCL-co-HA)) were carried out by Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) spectrometer (PerkinElmer, USA). Further analysis with FTIR was carried out on the lidocaine-loaded p(VCL-co-HA) NGs.
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4

Fiber Characterization via Multimodal Analysis

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Fiber morphology and diameter were examined using scanning electron microscopy (Zeiss Gemini 500 SEM) with an accelerating voltage of 2 kV. ImageJ™ open source software (National Institutes of Health) was used to measure the mean fiber diameters. Fifty measurements were taken for each sample from three separate images. Energy Dispersive X-ray spectroscopy (EDX) spectra were collected with an accelerating voltage of 10 kV. Samples were sputter coated with carbon for SEM and EDX. Chemical structure was analyzed with Attenuated Total Reflection-Fourier Transform Infrared (ATR-FTIR) spectroscopy (ATR-FTIR Spectrometer PerkinElmer Frontier) at each reaction step. Each spectrum was an average of 128 scans obtained between 4000 and 600 cm−1 at a resolution of 4 cm−1. Four spectra were collected per sample. Alkyne substitution was confirmed with Raman spectroscopy (Renishaw InVia Confocal Raman microscope). Each spectrum was obtained between 3250 and 200 cm−1 with an excitation wavelength of 785 nm and a resolution of ~1 cm−1. Three spectra were collected per sample. Crystalline structure was analyzed with X-ray diffraction (Bruker D8 Advance ECO powder diffractometer, 1 kW Cu-Kα source). Three spectra were collected per sample.
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5

FTIR Analysis of Samples

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The Fourier transform infrared spectra analysis (FTIR) of samples was conducted with an ATR-FTIR spectrometer (Perkin Elmer, Waltham, MA, USA). The scans were performed in an infrared region of 4000–450 cm−1, with an average of 64 scans.
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6

ATR-FTIR Analysis of Curcumin Nanoparticle Patches

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ATR-FTIR spectra of curcumin, chitosan, ethyl cellulose, nanoparticles, and patches were examined using the ATR-FTIR spectrometer (PerkinElmer, 940 Winter St Waltham, MA, United States). The samples were placed on the sample holder without any processing and scanned between 4000 and 400 cm−1. Spectra were recorded in triplicates and results were averaged [17 (link)].
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7

Characterization of Nano-Hydroxyapatite Composites

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FTIR spectra of the nano-hydroxyapatites and composite hydrogels were obtained from a Perkin Elmer, UATR two, ATR-FTIR spectrometer (Beaconsfield, Bucks, UK) in the wavelength range of between 4000–400 cm−1. Powder X-ray diffraction profile of hydroxyapatites and composite hydrogels was studied with Rigaku diffractometer, with Cu-Kα radiation at a voltage of 40 kV, current of 40 mA, and a scan rate of 0.02° s−1. The SEM/EDS (energy dispersive spectroscopy) analysis for nHA was carried out using the JEOL 6460LV scanning electron microscope at a voltage of 10 kV. The micro-morphology of composites were observed at a voltage 5 kV with a JEOL JSM-6610LV SEM. The samples were coated with gold by a sputter coater for excellent conductivity. Further gold coated hydrogel samples were air dried. The size and shape of the nHA-CS and nHA-MS nanoparticles were calculated by using the FEI Technai G2 20S-TWIN, USA transmission electron microscopy (TEM).
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8

ATR-FTIR Analysis of Curcumin Hydrogel

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ATR-FTIR spectra of Curcumin, CMC, essential oils, and the hydrogel were examined using the ATR-FTIR spectrometer (PerkinElmer, MA, USA). The samples were placed on sample holder and scanned between 4000–400 cm−1.
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9

ATR-FTIR Analysis of 5FU and Nanomaterials

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The ATR-FTIR analysis of 5FU, alginate, chitosan, 5FU-Alg nanoparticles and hydrogel were performed using PerkinElmer ATR-FTIR spectrometer (L1600300; PerkinElmer, Beaconsfield, UK). The sample was placed on zinc selenide, and the spectra was recorded in range of 600–4000 cm−1 (32 scans per minute with a resolution of 4 cm−1) in transmission mode. Three spectra of each sample were taken and the results were averaged.
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10

ATR-FTIR Analysis of Ileum and Colon Samples

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Ileum and colon samples of all animals were compressed on the Zn/Se crystal of the ATR unit (PerkinElmer) without any pretreatment and examined with an ATR‐FTIR spectrometer (PerkinElmer) at a resolution of 4 cm−1 and a scan number of 32. The spectra were obtained with the Spectrum One (PerkinElmer) software in the wavelength range of 4000–650 cm−1.16
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