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Nicolet 6700 fourier transform ir spectrometer

Manufactured by Thermo Fisher Scientific

The Nicolet 6700 Fourier transform IR spectrometer is a laboratory instrument used for infrared spectroscopy analysis. It utilizes Fourier transform infrared (FTIR) technology to collect and analyze infrared data from samples. The core function of the Nicolet 6700 is to measure the absorption and transmission of infrared radiation by samples, which can provide information about the molecular structure and composition of the materials being analyzed.

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2 protocols using nicolet 6700 fourier transform ir spectrometer

1

Nanofiber Characterization by XRD, Raman, SEM, and FTIR

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The nanofibers produced were characterized by conventional Bragg–Brentano X-ray diffraction (XRD) to evaluate the structure of the nanofibers. XRD was conducted to analyze the phase and crystallinity using a Rigaku X-ray diffractometer (Rigaku Co., Tokyo, Japan) with Cu Kα (λ = 1.54056 Å). The study used 2θ angles from 5° to 80°. A spectrometer (JY H800UV) equipped with an optical microscope was used to collect Raman spectra at room temperature with a radiation wavelength of 532 nm. Further, the (FE-SEM) field-emission scanning electron microscope (FE-SEM, Hitachi S-7400, Ibaraki, Japan) was employed to study the fabricated biocomposites’ structural features and chemical composition. All samples were coated with a platinum conductive material to prevent charge buildup on the specimen surface. The coating was thick enough to avoid charging but not thick enough to obscure specimen surface details. FTIR spectroscopy of the prepared samples was registered at a reflection mode by a model Thermo Nicolet 6700 Fourier transform IR spectrometer, in the range of 500–3000 cm−1 and with an accuracy of ±0.09 cm−1. The KBr disc method was used.
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2

Liposome Preparation and Characterization

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PC liposomes were prepared using the thin-film hydration method followed by extrusion with filters of decreasing diameter (400, 200 and 100 nm)45 (link). Lipids were hydrated with water with minimal metal impurities (Optima LC/MS Grade, Fisher Chemical). Liposomes were concentrated by filtration up to 72 mg/mL of lipid content. Lipid concentration was determined through the Rouser assay46 (link). Sodium salt was mixed and incubated at 37 °C (for 2 h) with the liposomes at a ratio of 16 mM X+:0.5 mg/mL lipids. Fourier-transform IR spectra of liposomes and liposomes incubated with alkali metals were collected afterwards with a Nicolet 6700 Fourier-transform IR spectrometer (Thermo Scientific) in transmission mode in liquid samples. All experiments were performed in triplicate.
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