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76 protocols using zetasizer nano series nano zs

1

Dynamic Light Scattering of Aggregates

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Dynamic light scattering (DLS) measurements were carried out at 25.0 ± 0.1 °C using a light-scattering instrument (Zetasizer, nanoseries, nano-ZS, Malvern Instruments, Malvern, UK) with a He−Ne laser (633 nm, 4 mW) equipped with a built-in temperature controller. For each sample, 30 repeated measurements were taken. From the DLS data, the CONTIN algorithm was used to determine the size distribution of aggregates.
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2

Physicochemical Characterization of Nanocarriers

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The particle size (hydrodynamic diameter) and polydispersity-index (PDI) of the NCs were measured by Differential Light Scattering (DLS) technique using Zetasizer Nanoseries, (Nano-ZS, Malvern Instruments, Worcestershire, UK). The results are the mean particle size, which is the intensity versus average diameter/thickness of the NCs majority population, and PDI is the measure of the size distribution width. The suspension of NCs was diluted with Milli-Q® water to get their appropriate concentration and the mean values were calculated from three measurements. The zeta-potential (ZP) of the NCs was measured by the same instrument at ambient temperature in the original dispersion medium of the NCs (aqueous solution of stabilizer with and without mannitol). The installed software (DTS Version 4.1, Malvern, Worcestershire, UK) with this instrument automatically measured the electrophoretic mobility of the NCs and transformed it to zeta potential using the “Helmholtz-Smoluchowski equation”.
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3

Characterizing CREKA-Lipo Nanoparticle Properties

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The size distribution and zeta potential of CREKA-Lipo-anti-IFNγ and CREKA-Lipo were assessed by dynamic light scattering (DLS) using the ZetaSizer Nano series Nano-ZS (Malvern Instruments Ltd., Malvern, UK).
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4

Zeta-Potential Measurement of Rock Particles

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Zeta-potential measurements were performed on ZetaSizer nano series - Nano-ZS (Malvern Instruments Ltd., United Kingdom). The instrument measures the direction and velocity of a particle in an applied electrical field via phase analysis light scattering and laser Doppler velocimetry. The calculated electrophoretic mobility is converted into zeta potential values using the Smoluchowski model. Before measuring the rock particles or emulsions in surfactants solutions, the zeta-potential of surfactant solutions was determined to make sure the results of rock particles or emulsions will not be interfered by surfactants aggregates.
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5

Nanoparticle Characterization using DLS and ELS

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Particle size expressed as hydrodynamic diameter and size distribution expressed as polydispersity index (PdI) were determined using dynamic light scattering (DLS), while ζ-potential measurements were based on electrophoretic light scattering (ELS). All measurements were conducted in a ZetaSizer Nano series Nano-ZS (Malvern Instruments Ltd., Malvern, UK) equipped with a He-Ne Laser beam, set up in a wavelength of 633 nm and backscattering angle of 173°. Settings for ζ-potential measurement contained an average of 100 runs with the phase analysis light scattering mode (PALS) and equilibration temperature of 25 °C. NPs dispersion in water was prepared by dispersing 5 mg of NPs in 10 mL of water. All measurements were carried out in triplicate.
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6

Zeta Potential Measurement of Polymers

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Positive or negative charges of polymeric solutions were measured by laser Doppler electrophoresis using a using a Zetasizer nanoseries Nano ZS (Malvern Instruments Ltd., Malvern, UK). Data analysis of Zeta potential is presented as mean standard deviation of three samples (with ten runs for each sample).
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7

Nanoparticle Size Analysis by DLS and SEM

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Size distribution was determined with Dynamic Light Scattering (DLS) using a Zetasizer Nanoseries Nano-ZS (Malvern Panalytical, Malvern, UK) at 23 °C. Briefly, a sample of nanoparticles dissolved in citric acid (0.3%) was analysed for three sessions of 90 runs of 90 s each. SEM analysis was performed on a 10 µL sample.
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8

Characterization of Monodisperse Nanoemulsions

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A Malvern Mastersizer MS 3000 (Malvern Instruments Ltd., Cambridge, UK) was employed to evaluate the droplet sizes and polydispersity indexes. ζ-potential values were estimated by employing a particle electrophoresis instrument (Zetasizer Nanoseries Nano-ZS, Malvern Instruments, Worcestershire, UK). Different emulsions were diluted 100 times with citric buffer before measurement. All measurements were performed in triplicate and reported values were given as average ± standard deviation. At ΦI = 0.038, the average droplet size was 478 ± 58 nm. The polidispersity index (PDI) was 0.22, suggesting that nanoemulsions were essentially monodisperse. The ζ-potential of the nanoemulsions was −15 mV, according to the non-ionic nature of the surfactant Tween 80. Note that the destabilization process was not observed by the naked eye for more than 3 months. Figure 1 shows a TEM photograph of the nanoemulsions prepared in this work.
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9

Characterization of Modified Cellulose Nanocrystals

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DLS and ζ potential
measurements were carried out with Zetasizer
Nano Series (NANO-ZS) equipment from Malvern Instruments for diluted
dispersions (0.01 wt %) of CNC, CNC-g-POx, and physical
mixtures of pristine and modified CNCs prepared by freeze-drying and
redispersion in water at 0.01 wt % in different mass ratios (CNC/CNC-g-POx, 0:1, 1:1, 2:1, 4:1, 10:1, w/w).
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10

Characterization of Nanoparticle Size and Zeta Potential

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The intensity-averaged particle diameters and polydispersity indices of the NPs were determined by dynamic light scattering (DLS) with 173° backscatter detection. The electrophoretic mobility values, measured by laser Doppler velocimetry, were converted to zeta potential by the Smoluchowski equation. Both DLS and LDV measurements were performed on a Zetasizer nano series Nano-ZS fitted with a 633 nm laser (Malvern Instruments, Malvern, UK). The measurements were performed at an NP concentration of approximately 0.3 mg/mL, obtained by 30-fold dilution of 10 mg/mL dispersion with MilliQ water. Each analysis was carried out at 25 °C in triplicate.
Particle morphology was evaluated by scanning electron microscopy (SEM). A strip of double-sided carbon tape was placed on a SEM stub. A small quantity of freeze-dried NPs was gently spread across the surface of the tape, and compressed air was used to remove loose particles. Samples were sputter-coated with carbon for 20 s and viewed under a Hitachi S-4800 scanning electron microscope (Hitachi High-Technologies Corporation, Hitachi, Japan).
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