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Inova ft 500 spectrometer

Manufactured by Agilent Technologies

The Inova FT-500 is a Fourier Transform Nuclear Magnetic Resonance (FT-NMR) spectrometer designed for routine laboratory analysis. It is capable of performing high-resolution NMR spectroscopy on a variety of sample types. The instrument utilizes a superconducting magnet to generate a strong, stable magnetic field for the NMR analysis.

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5 protocols using inova ft 500 spectrometer

1

Polymer Nanoparticle Characterization Methods

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Proton nuclear magnetic resonance (Varian Inova FT-500 spectrometer) and gel permeation chromatography (PL-GPC-220 instrument) were used for polymer characterization. NMR spectra were recorded on a Varian Inova FT-500 spectrometer. The morphology of the nanoparticles was characterized by using Transmission Electron Microscopy (TEM). Zetasizer Nano ZS (Malvern Instruments) and Jeol JEM 2100 transmission electronic microscope (Oxford Link EDS detector and Digital MicrographTM software from Gatan) were employed for nanoparticle characterization.
The efficiency of the Loading (LE) and encapsulation (EE) were calculated according to:

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2

Polymer Microstructure Analysis by NMR

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NMR spectra were recorded on a Varian Inova FT-500 spectrometer and were referenced to the residual deuterated solvent signal. The microstructures of PLA samples were determined by examination of the methine region in the homodecoupled 1 H NMR spectrum of the polymers recorded at room temperature in CDCl 3 on a Varian Inova FT-500 spectrometer with concentrations in the range 1.0 to 2.0 mg/mL.
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3

Characterization of PLA Microstructures

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The NMR spectra of complexes were recorded on a Varian Inova FT-500 spectrometer and were referenced to the residual deuterated solvent signal. 1H NMR homodecoupled and NOESY-1D spectra were recorded on the same instrument with the following acquisition parameters: irradiation time 2 s and 256 scans, using standard VARIAN-FT software. Furthermore, 2D NMR spectra were acquired using the same software and processed using an IPC-Sun computer.
The microstructures of PLA samples were determined by examination of the methine region in the homodecoupled 1H NMR spectrum of the polymers recorded at room temperature in CDCl3 with concentrations in the range 1.0 to 2.0 mg/mL.
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4

Characterization of DAS-loaded Nanoparticles

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1H nuclear magnetic resonance (NMR) spectra were recorded on a Varian Inova FT-500 spectrometer. Gel permeation chromatography (GPC) measurements were performed on a Polymer Laboratories PL-GPC-220 instrument equipped with a TSK-GEL G3000H column and an ELSD-LTII light-scattering detector. Field Emission Scanning Electron Microscopy (FE-SEM) images were recorded on a Jeol 7800 F electron microscope to study the particle size distribution and morphology of the nanoparticles. High-resolution electron microscope images were obtained on a Jeol JEM 2100 transmission electron microscope (TEM) operating at 200 kV and equipped with an Oxford Link EDS detector. As the specimens could be damaged under beam irradiation, observation was performed under low-dose conditions. The resulting images were analyzed using Digital Micrograph™ software from Gatan. The average sizes, polydispersities and Z-potentials of the formulations were measured using a Zetasizer Nano ZS (Malvern Instruments). Data were analyzed using the multimodal number distribution software included in the instrument.
Loading efficiency (LE) and encapsulation efficiency (EE) of DAS were calculated according to the following equations:
LE% = (weight of encapsulated DAS (mg))/(weight of total (DAS encapsulated+scaffold weight) (mg)) × 100%
EE% = (weight of encapsulated DAS (mg))/(weight of DAS feeding (mg)) × 100%
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5

Characterization of Polymeric Compounds by NMR and GPC

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NMR spectra were recorded on a Varian Inova FT-500 spectrometer and were referenced to the residual deuterated solvent signal. 1 H NMR homodecoupled and NOESY-1D spectra were recorded on the same instrument with the following acquisition parameters: irradiation time 2 s and 256 scans, using standard VARIAN-FT software. 2D NMR spectra were acquired using the same software and processed using an IPC-Sun computer.
Microanalyses were performed with a Perkin-Elmer 2400 CHN analyzer. The specific rotation [a] D 22
was measured at a concentration of 0.1% w/v in toluene or chloroform at 22 ºC on a JASCO P2000
Polarimeter equipped with a sodium lamp operating at 589 nm with a light path length of 10 cm.
The molecular weights (M n ) and the molecular mass distributions (M w /M n ) of polymer samples were measured by Gel Permeation Chromatography (GPC) performed on a Shimadzu LC-20AD GPC equipped with a TSK-GEL G3000Hxl column and an ELSD-LTII light-scattering detector. The GPC column was eluted with THF at 40 ºC at 1 mL/min and was calibrated using eight monodisperse polystyrene standards in the range 580-483 000 Da.
MALDI-ToF MS data were acquired with a Bruker Autoflex II ToF/ToF spectrometer, using a nitrogen laser source (337 nm, 3 ns) in linear mode with a positive acceleration voltage of 20 kV. 3,3´) .
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