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Zetasizer nano s equipment

Manufactured by Malvern Panalytical
Sourced in Germany, United Kingdom

The Zetasizer Nano S is a dynamic light scattering (DLS) instrument designed for the measurement of particle size and zeta potential. It can determine the size of particles, molecules, and proteins in the range of 0.3 nanometers to 10 micrometers.

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3 protocols using zetasizer nano s equipment

1

Optical and Colloidal Characterization of M-SPIONs

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The optical characterization of M-SPIONs dispersed in aqueous medium was performed at 50 µg Fe/mL using an RF-6000 spectrofluorophotometer (Shimadzu, Kyoto, Japan) to acquire the spectrum with excitation in the wavelength range from 520 to 800 nm and emission from 550 to 780 nm.
The polydispersion of hydrodynamic diameter (HD), temporal stability of HD and zeta potential of M-SPIONs (50 µg Fe/mL) were measured using dynamic light scattering (DLS) with Zetasizer Nano S equipment (Malvern, Reino Unido). The HD distribution curve was obtained using an angle of 173 degrees with 15 measurements in 5 s, maintaining a constant temperature at 37 °C. M-SPION HD stability analysis was performed in cell culture medium (DMEM +10% FBS) for 20 h. The zeta potential measurements (surface charge) were performed in the pH range from 7 to 9.
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2

Synthesis and Characterization of Silver Nanoparticles

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An AgNO3 solution of 1 × 10−3 M concentration was prepared by dissolving 18 mg of the salt in 100 mL of distilled water; the solution was stirred until complete dissolution; then, it was adjusted to pH 8 with a 1 M solution of NaOH. The solution was heated at 85 °C under continuous stirring for 10 min, during this process, 1 mL of sodium citrate solution (1% w/v) was added. The solution was kept on the heat for one hour at 85 °C; until the solution acquired a brownish color [44 (link)]. After that, it was cooled at room temperature, obtaining a suspension of 18 µg/mL. The absorbance of the colloidal system was determined by UV-vis spectroscopy in a Specord 200 plus spectrophotometer (Analytik Jena AG, Jena, Germany).
AgNP size was determined using Malvern Zetasizer Nano S equipment and DTS (nano) software from Malvern instruments, Madrid, Spain. Diluted samples were sonicated for 10 min to deagglomerate the nanoparticles; then, the suspension was placed in disposable polystyrene cuvettes, and the scattering intensity was measured at 25 °C. Water was used as the dispersant. The analysis was carried out by triplicate, and several records were performed in each analysis.
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3

Characterizing Vesicular Formulations

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The mean size and polydispersity index (PDI) of UDV were determined by dynamic light scattering with Zetasizer Nano-S equipment (Malvern Instruments, Malvern, UK). PDI less than 0.2 indicates a homogenous and monodisperse population. Zeta potential was determined by laser-Doppler anemometry with Zetasizer Nano-Z equipment (Malvern instruments)
For both measurements, 10 µL of transfersome, transethosome, and ethosome formulations were diluted with purified water.
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