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76 protocols using zetasizer nano zs apparatus

1

Determining Cell Membrane Surface Charge

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In order to determine surface charge density of cell membrane, cells were suspended in 0.9 % NaCl and put into the measuring vessel; then, electrophoretic mobility was measured using Zetasizer Nano ZS apparatus (Malvern Instruments). The measurements were carried out as a function of pH.
The surface charge density has been determined using equation σ = ηu/d, where u is the electrophoretic mobility, η is the viscosity of solution, and d is the diffuse layer thickness [16 ].
The diffuse layer thickness was determined from the formula [1 ]: d=ε·ε0·R·T2·F2·I , where R is the gas constant, T is the temperature, F is the Faraday number, I is the ionic strength of 0.9 % NaCl, and εεo is the permeability electric medium.
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2

Zeta-potential of TiO2 Nanoparticles

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Zeta-potential was determined in diluted TiO2 NP stock dispersions and TiO2 NP/BSA dispersions (100 and 10 μg/ml) measuring electrophoretic mobility of the particles at 20 °C via laser Doppler velocimetry using a Zetasizer Nano-ZS apparatus (Malvern Instruments Ltd.) and disposable capillary cuvettes (Malvern Instruments Ltd.). Three consecutive measurements were taken of each sample. The number of runs was set automatically. The Smoluchowski approximation was used for calculation.
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3

Comprehensive Characterization of Graphene-Based Nanocomposites

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The synthesized materials were morphologically characterized by high resolution transmission electron microscopy (HR-TEM, Hitachi-HT7700, 120kv, Japan) to investigate the sheet-like morphology of rGO, and the formation of AuNPs and their size and dispersion patterns. A few drops of each sample were allowed to air-dry on a lacy copper grid coated with carbon film for TEM analysis. Graphene structural features were revealed using Raman spectroscopy (Renishaw inVia Raman, Gloucestershire, UK) with a 514 nm argon gas laser. Fourier-transform infrared spectroscopy (FT-IR) analysis was performed to detect functionalization, wherein the sample powder was ground with potassium bromide (KBr) into thin pellets. FT-IR spectra were recorded using a Spectrum 400 (PerkinElmer, Boston, MA, USA). X-ray diffraction patterns (XRD) were recorded using an EMPYREAN diffraction system with X-ray wavelength of 1.54060 Å. UV-Vis spectroscopic measurements were performed using PerkinElmer–Lambda 35 spectrophotometer at a wavelength range of 200–800 nm. Thermo-gravimetric analysis (TGA) was performed using a TGA/SDTA 851 (Mettler Toledo, USA) system with a heating rate of 10°C/min up to 800°C in a nitrogen environment. Dynamic light scattering (DLS) of CAG nanocomposite in cell culture RPMI-1640 medium was analyzed using Zetasizer Nano-ZS apparatus (Malvern Instruments, UK) at 25°C.
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4

Hydrodynamic Size Monitoring of Ag 75 Cit NPs

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The hydrodynamic size of the Ag 75 Cit NPs in water and in cell culture medium was monitored using a Zetasizer Nano ZS apparatus (Malvern Instruments GmbH, Herrenberg, Germany).
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5

Analyzing AmCD–Alg Aggregate Dimensions

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DLS measurements to evaluate the possible dimensions of AmCD–Alg aggregates were performed with a Malvern Instruments Zetasizer NANO-ZS apparatus. The intensity of the diffused light was evaluated at 173°; autocorrelation functions were analysed by means of the cumulants method using the Sasfit 0.94.4 software package. Samples were prepared in aqueous buffer at either pH 6.5 or pH 8.4, by mixing the proper amounts of Alg with each AmCD in such a way to have concentrations as large as 0.25 mN for Alg and 1.5 mM for the AmCD. The turbid mixtures obtained were allowed to settle for 24 h and then, the apparently clear supernatant liquors were carefully pipetted and analysed.
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6

Morphological Analysis of PLGA Nanoparticles

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To examine the morphology of the fabricated PLGA nanoparticles, a field emission scanning electron microscope (SEM) was used (FE-SEM, Quanta FEG-650, USA). Prior to scanning, the PLGA nanoparticles were coated with an Au-Pd sputter to enhance surface conductivity while reducing charging artifacts. An accelerating voltage of 20 kV was used in most cases, and the SEM images were processed at the UAB SEM Laboratory. Zeta potentials (the electrostatic potential at the electrical double layer surrounding a nanoparticle in solution) were determined by using a Malvern Zetasizer Nano ZS apparatus (Malvern Instruments Ltd, Worcestershire, UK).
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7

Characterization of DOX@ZIF-8 Nanostructures

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The morphology of DOX@ZIF-8 before and after functionalization was observed using JEOL-2100 transmission electron microscopy (TEM) at an operating voltage of 200 kV. Field-emission scanning electron microscopy (FESEM) was performed on a Hitachi S-4800 (Japan). An X-ray diffraction (XRD) pattern was produced on a Rigaku D/MAX-2550 PC diffractometer using monochromic Cu-Kα radiation operated at 40 kV and 80 mA in a 2θ range of 10–50°. The size distribution of DOX@ZIF-HA in different media was measured by dynamic light scattering (DLS) on a BI-200SM multiangle dynamic/static laser scattering instrument (Brookhaven, U.S.). Zeta potential measurements were performed on Malvern Zetasizer Nano ZS apparatus. A Fourier transform infrared (FTIR) spectrum was recorded using a Nicolet 6700 spectrometer.
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8

Characterization of Nanomaterial Properties

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Photon Correlation Spectroscopy (PCS) was used to evaluate the mean diameter, size distribution and zeta potential of the systems using a 1:50 dilution and applying the third-order cumulant fitting correlation function (Zetasizer Nano ZS apparatus, Malvern Panalytical Ltd., Spectris plc, Malvern, UK) [37 (link)]. Transmission Electron Microscopy (TEM) was used in order to investigate the morphology of the nanosystems, as previously described [35 (link),37 (link)].
Moreover, a Turbiscan Lab Expert® apparatus (Formulaction, Toulouse, France) was employed with the aim of evaluating the stability of the various samples; the results were processed using Turby Soft 2.0 software (Formulaction, Toulouse, France) and expressed as Turbiscan Stability Index (TSI) as a function of time and temperature [35 (link),38 (link)].
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9

Liposome Preparation by Dehydration-Rehydration

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The liposomes were prepared based on the conventional dehydration–rehydration method as previously reported.9 (link)–11 Ten micromoles of lipids in chloroform (a lipid composition of DOPC:DOPG:MPB = 4:1:5 molar ratio was typically used) were dispensed into small round-bottom flasks, and the organic solvents were evaporated under nitrogen overnight to prepare dried thin lipid films. The lipid films were rehydrated at room temperature in 1 mL 0.2 M bis-tris buffer at pH 7.0 for 1 h with rigorous vortexing for 30 s every 5 min, and then sonicated in alternating power cycles of 8% amplitude (~30W) in 30 s intervals for 5 min on ice. The resulting liposomes were extruded 21 times through a 0.2 µm polycarbonate membrane (Whatman, Piscataway, NJ, USA) using an Avanti Mini-Extruder (Avanti Polar Lipids Inc., Alabaster, AL, USA). The liposome solutions were freshly made and used shortly after preparation to avoid the ring-opening (hydrolysis) reactions of the maleimide moieties, which might prevent them from further reactions.66 (link) The average size of the monodisperse liposomes was analyzed via DLS at 25 °C on a Malvern Zetasizer Nano ZS apparatus with Malvern Instruments DTS software (v.6.01) using the cumulants fit (Malvern Instruments, Malvern, Worcestershire, UK).
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10

Characterization of Nanoparticle Systems

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The average diameter, size distribution and surface charge of the various systems were evaluated by the dynamic light scattering (DLS) technique using a Zetasizer NanoZS apparatus (Malvern Panalytical Ltd., Spectris plc, Malvern, UK) by diluting each sample at a 1:50 ratio in MilliQ water [19 (link)]. Transmission Electron Microscopy (TEM) was used to perform the morphological characterization of the nanosystems [24 (link)].
The stability of the samples was investigated as a function of time and temperature with a Turbiscan Lab® Expert (Formulaction, Toulouse, France) and expressed as variation of the Turbiscan Stability Index; data were processed using a TurbiSoft 2.0, as previously reported [28 (link)].
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