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11 protocols using resolution pro software

1

FTIR Spectroscopic Analysis of PrP Conformations

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FTIR spectra were acquired on a Varian FTS-7000 infrared spectrometer (Varian) equipped with a DTGS (deuterated triglycine sulfate) detector. MoPrPc 23–231, MoPrP 23–231 oligomers and MoPrP 23–231 fibril samples (50 µL of 2–3 mg/mL) were dried onto a CaF2 plate under nitrogen. Spectra were acquired from 96 scans at a sensitivity of 2 and a resolution of 2 cm−1. First a background scan was run with a CaF2 plate in place and then a blank spectrum was acquired with buffer dried onto the CaF2 plate. Spectra were smoothed with a Savitsky-Golay window of 9 points using the Varian Resolution Pro software. FTIR spectra were further processed using Origin (Version 9) to assist with spectral deconvolution and secondary structure quantification. The second derivatives of the smoothed spectra were calculated using Origin (Version 9) with 2nd order Savitsky-Golay smoothing and a 9-point window. Before deconvolution, the baseline was subtracted from each absorbance spectrum. Absorbance spectra were then deconvoluted using Origin's multiple peak fit, employing non-linear Lorentz curve fitting by fixing the wavenumber of the peak maxima from the second derivative spectra and using a peak width of 20 cm−1. The deconvoluted spectrum was then fit to multiple Gaussian curves by fixing the peak wavenumbers using the second derivative of the deconvoluted spectra and fixing the peak width to 13 cm−1.
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2

FTIR Analysis of Dried Alzheimer's Samples

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Small samples (<1 mg) of dried AD-EM, EM, and AD were each ground into a fine powder with a mortar and pestle. Dried potassium bromide (KBr, 0.1 g) was added to the powdered drug sample and ground into a fine powder. Each sample was placed in a 13 mm die and pressed with a force of 10 metric tons for 10 min. Each pellet was removed from the die and scanned in an Excaliber Series-BioRad FTS3000MX spectrometer. Then, 200 background and 400 sample scans were collected from 500–4000 cm−1. Varian Resolution Pro Software was used to transform the data using ratio and transmittance transformations. A boxcar function was used to smooth out each plot.
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3

FTIR Characterization of Solid Samples

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The
coatings were removed from the flat surfaces and homogenized in an
agate mortar and pestle. They were then mixed with approximately 40
mg of IR grade KBr powder (Sigma-Aldrich, Germany) and pressed into
a pellet using a manual hydraulic press (2 tons, room temperature,
Wasserman, Germany). The spectra were recorded in transmission mode
with an Agilent 660 FTIR spectrometer (Agilent Technologies) with
a DTGS detector at 4 cm–1 resolution and averaging
of 32 scans between 4000 and 400 cm–1 using Resolution
Pro software (Agilent Technologies; Germany).
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4

Evaluating Collagen Quality via EA-IRMS

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To assess the quality of the collagen, all extracts were analysed via EA-IRMS to obtain elemental (C%, N%, C:N) and stable isotopic data (δ13C and δ15N). Collagen (ca. 400 μg) was weighed into tin cups using a microbalance and measured on a ThermoFinnigan Flash EA coupled to a Thermo Delta plus XP isotope ratio mass spectrometer (IRMS). Stable carbon isotope ratios were expressed relative to VPDB (Vienna PeeDee Belemnite) and stable nitrogen isotope ratios were measured relative to AIR (atmospheric N2), using the delta notation (δ) in parts per thousand (‰). Repeated analysis of both internal and international standards indicates an analytical error of 0.2‰ (1σ) for δ13C and δ15N. Where sufficient material was available, collagen (ca. 300 μg) was homogenized and mixed with ∼40 mg of IR grade KBr powder in an agate mortar and pestle, pressed into a pellet using a manual hydraulic press (Wasserman) and analysed with an Agilent Technologies Cary FTIR Spectrometer with a DTGS detector. Spectra were recorded in transmission mode at 4 cm−1 resolution with averaging of 34 scans between 4000 and 400 cm−1 using Resolution Pro software (Agilent Technologies). The spectra were evaluated and compared to library spectra of well-preserved collagen and bone to look for evidence of incomplete demineralisation, degraded collagen or the presence of any exogenous material in the extracts.
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5

Infrared Spectroscopic Analysis of Salbutamol-Soluplus Interaction

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Potential interaction between salbutamol and soluplus in the formulation matrix was assessed using an infrared spectrometer, Varian 3100, from Varian Inc., Palo Alto, CA, USA. Approximately 3 mg of the powder formulation was placed on the attenuated total reflection (ATR) accessory unit, and a total of 64 scans were collected (400–1900 cm−1) with a resolution of 4 cm−1. The spectra were collected, and the peak position was analyzed using the Resolution Pro software from Agilent Technologies Inc., Santa Clara, CA, USA.
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6

FTIR Analysis of Collagen Extracts

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For the collagen extracts from Experiment B, ca. 0.3 mg collagen was homogenised and mixed with ∼40 mg of IR grade KBr powder in an agate mortar and pestle, pressed into a pellet using a manual hydraulic press (Wasserman) and analysed with an Agilent Technologies Cary FTIR Spectrometer with a DTGS detector. Spectra were recorded in transmission mode at 4 cm−1 resolution with averaging of 34 scans between 4000 and 400 cm−1 using Resolution Pro software (Agilent Technologies). The spectra were analysed and compared to library spectra of well-preserved collagen and bone.
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7

FTIR Analysis of Sample Materials

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FTIR analysis was conducted on an attenuated total reflectance (ATR) FT-IR spectrometer (Cary 600 series FTIR spectrometer, Agilent Technologies, Santa Clara, CA, USA). Spectra were collected from 800 to 4000 cm−1 with a resolution of 4 cm−1. The scan number of 256 was used for both background and samples. The obtained spectra were analyzed to using ResolutionPro software (Version 5.2.0, Agilent Technologies, Santa Clara, CA, USA).
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8

FTIR Characterization of Freeze-Dried Powders

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FTIR (Cary 630 FTIR, Agilent Technologies, Virginia, USA) was used for structural characterization of the freeze dried powder samples. The analysis was carried out using the Resolution Pro software version 2.5.5 (Agilent Technologies, USA).
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9

FTIR Spectral Characterization of Samples

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Fourier Transform Infrared (FTIR) spectra were recorded by placing approximately 2 mg of the sample on the GladiATR accessory (Pike Technologies, Madison, USA) equipped in a Varian 3100 FTIR spectrometer (Varian Inc., California, CA, USA). The spectra were collected at a 4 cm−1 resolution with 64 scans over a range of 400–4000 cm−1 using Resolution Pro software (Agilent Technologies Inc., California, CA, USA). Peak positions were also identified using the same software.
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10

ATR-FTIR Analysis of Serum Samples

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ATR-FTIR spectra were collected using a Cary-600 series FTIR spectrometer (Agilent Technologies, Santa Clara, California) with a MIRacle™ single reflection ATR configured with a diamond (Di) IRE plate (PIKE Technologies, Fitchburg, Wisconsin). 32 co-added scans, covering a wavenumber range of 4000 to 600 cm -1 , were combined to produce the spectrum, using a spectral resolution of 4 cm -1 . A background spectrum of the ambient conditions was automatically subtracted by the Resolution Pro software (Agilent Technologies) to produce each sample spectrum.
For every patient, three measurements of the same 1 μL serum aliquot were taken immediately following deposition. After the optimal drying time of 8 minutes, determined from previous drying experiments [16] , the same 1 μL serum aliquot was analyzed in triplicate again.
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