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193 protocols using sz 100

1

Characterizing rPF4 Tetramerization and Complexation

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The secreted rPF4 tetramerization and rPF4-heparin complex formation were studied using dynamic light scattering (DLS) technique (Nanopartica SZ 100; HORIBA Ltd, Kyoto, Japan) with a fixed 173 scattering angle and a 633-nm helium-neon laser. Data were analyzed using a Horiba SZ 100 apparatus for Windows [Z Type] software version 2.20 (Nanopartica SZ 100; HORIBA Ltd, Kyoto, Japan). Furthermore, Zeta potential experiments were performed, employing Horiba SZ 100.
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2

Characterizing CBZ NLC Particle Size

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The particle size of CBZ NLC was determined using dynamic light scattering (Horiba, SZ 100, Japan). NLC dispersion was diluted with distilled water and ultrasonicated for 10 minutes followed by measurement at fixed angle 90° at 25°C carried out in triplicate. For zeta potential analysis, the sample was diluted by conducting solution and zeta potential was measured (Horiba, SZ 100, Japan).19 (link)
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3

Characterizing Emulsion Droplet Size and Charge

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The emulsion droplet size was measured using a dynamic light scattering instrument (SZ-100; Horiba, Kyoto, Japan). The refractive index of menhaden oil and 10 mM phosphate buffer was set to 1.465 and 1.333, respectively. To avoid multiple scattering effects, the emulsion was diluted 1000-fold with 10 mM phosphate buffer with the same pH as the emulsion, prior to measurement.
The surface charge (ζ-potential) of the emulsion droplets was measured by measuring the ζ-potential of the emulsions using a laser Doppler microelectrophoresis instrument (SZ-100; Horiba, Kyoto, Japan). To minimize the effect of multiple scattering, the sample was diluted with 10 mM phosphate buffer that had the same pH as the sample, and the diluted sample was placed into disposable capillary cells (Horiba, Kyoto, Japan).
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Droplet Size Characterization of HIPEs

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The droplet size of the HIPEs was determined using a particle size analyzer (SZ-100, Horiba, Japan). Samples were diluted appropriately (100-fold) with phosphate buffer solution (10mM, pH 7) and the z-average diameter (nm), as well as the polydispersity index (PI), were measured.
The refractive indices of soybean oil and phosphate buffer solution were 1.46 and 1.33, respectively.
The zeta potential of the emulsions was assessed by dynamic light scattering (DLS) using a Zetasizer (SZ-100, Horiba, Japan). All the samples were diluted appropriately before the analysis (to avoid multiple scattering effects) and measured at 25 °C.
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5

Characterization of Emulsions and Nano-emulsions

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Average diameters and polydispersity (PDI) indices of emulsions and nano‐emulsions were determined by the DLS method of Hosseinnia, Khaledabad, and Almasi (2017). The DLS method is based on vibrations corresponding with different intensities, produced by the Brown motion of particles along with the change in position in space. Dynamic light scattering (DLS) techniques use HORIBA SZ‐100 instrument. All measurements were carried out at 25°C. The plotting of particle size distribution was carried out directly by the HORIBA SZ‐100 instrument.
The GC‐MS (gas chromatography–mass spectrometry) method was used for determining the chemical components in the compound.
Viscosity was measured by a rotary viscometer, the Rion Viscotester VT‐04 (Japan), based on viscosity changes over time to determine the stability of nano‐emulsions.
Transmission electron microscopy (TEM) is a technique that studies microstructures of solid objects. The high‐energy electron beams from the instrument penetrate through specimens and lenses were used to create images, resulting in the magnification level of up to 400,000 times for most of materials and millions of times for atoms. Images were recorded with a digital camera on fluorescent screens or optical films.
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6

Nanoparticle Characterization by DLS

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Mean particle size and size distribution analysis were performed using the dynamic light scattering technique (SZ-100, Horiba scientific, Kyoto, Japan) at 25°C. Zeta potentials (SZ-100, Horiba scientific, Kyoto, Japan) were measured to evaluate surface charge and stability of particles. These prepared NPs were diluted in deionized water (1/10, w/v) and placed in measurement cell for analysis (n = 5).
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7

Droplet Size and Zeta Potential Characterization

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The volume-weighted mean droplet size and distribution width (Span) were studied using dynamic light scattering (DLS) (SZ100, Horiba, Kyoto, Japan) at 20 °C.
The electrical surface charge of the samples was investigated by DLS (SZ100, Horiba, Japan) at room temperature according to the Smoluchowski equation (Equation (1)).
μe=ε ζ η 
where μe is the electrophoretic mobility (m2 s−1 V−1), ε is the permittivity (J V−2 m−1), ζ is the zeta potential (V), and η is the viscosity (g m−1 s−1).
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8

Physicochemical Characterization of Nanoemulsions

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We assessed droplet size by dynamic light scattering (DLS; SZ-100, Horiba Scientific, Kyoto, Japan), and we measured zeta potential of nanoemulsion using a zeta potential analyzer (SZ-100, Horiba Scientific, Kyoto, Japan). The prepared nanoemulsion was diluted with DIW (1/20, w/v) and gently mixed for 1 min. The samples were loaded on the measurement cells maintained at 25 °C. The pH of prepared formulation was determined using a pH meter (SevenEasy, Mettler-Toledo, Zürich, Switzerland). We performed these preparation procedures twice more and evaluated the physicochemical properties through the same process as above.
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9

Characterization of Silver-Nisin Nanocomposites

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Fourier transform infrared spectroscopy (FTIR) (FT/IR-6300, JASCO Corporation, Tokyo, Japan) was used to investigate the composition and structure of Ag-nisin. Field emission scanning electron microscopy assessment (FESEM) (MIRA3, Tescan, Czech Republic) was used to examine the particle sizes and morphology of the AgNP samples that had been prepared.
The nanoPartica SZ-100 HORIBA made in Japan was employed to investigate the size distribution and stability of AgNPs (dynamic light scattering [DLS]), as well as zeta potential measurements.
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10

Extracellular Vesicle Internalization in MG63 Cells

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MG63 cell line was cultured in the presence of RPMI containing 10% FBS (Gibco), 1% L-glutamine (Bioidea), and 1% penicillin/streptomycin (Gibco) at 37 °C and 5% CO 2 . ECVs were labeled with PKH26, using PKH26 red fluorescent cell linker kit (Sigma) according to the manufacturer's protocol. Briefly, 0.5 mL of ECVs mixed with 498 µL of dilution buffer and 2 µL PKH26 and incubated for 5 min and diluted with FBS at a ratio of 50/50. Then, the mixture was centrifuged at 100 000 g for 90 minutes at 4 °C. The pellets were mixed with 1 mL of the culture medium. Labeled ECVs were added to MG63 cell line cultures and incubated for 22 hours. Finally, the internalization of the labeled ECVs was evaluated by fluorescence microscopy. For negative control, the same amount of dilution solution without ECVs was added to the cells.
Dynamic Light Scattering (DLS)
ECV size was evaluated by nanoparticle analyzer (SZ-100 Horiba, Japon) equipped with a 532-nm wavelength, 10 mW power, and operating at an angle of 173. ECVs were transferred to cuvettes (ZEN0040, Malvern, Herrenberg, Germany). The measurements were made at a fixed position and at 25 °C. Three independent measurements were performed for each sample, and three samples were analyzed, and the mean value calculated.
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