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.
Zetasizer nano s equipment
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.
3 protocols using zetasizer nano s equipment
Optical and Colloidal Characterization of M-SPIONs
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.
Synthesis and Characterization of Silver Nanoparticles
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.
Characterizing Vesicular Formulations
For both measurements, 10 µL of transfersome, transethosome, and ethosome formulations were diluted with purified water.
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