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Zetasizer pro red label

Manufactured by Malvern Panalytical
Sourced in United Kingdom

The Zetasizer Pro Red Label is a dynamic light scattering (DLS) instrument used for particle size and zeta potential analysis. It measures the size and charge of particles in the nanometer to micrometer range. The instrument utilizes a red laser light source and is designed for a wide range of applications, including materials characterization, pharmaceuticals, and colloid science.

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3 protocols using zetasizer pro red label

1

Characterizing Transethosomes and LNPs

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Dynamic light scattering was used to determine the hydrodynamic diameter and zeta potential of empty and natamycin-loaded transethosomes and LNPs. Measurements were performed with a Malvern Zetasizer Pro Red Label (Malvern, Worcestershire, UK), with backscatter collection angle (173°) and keeping the temperature at 25 °C. The reported values for size and zeta potential are the means of three experiments performed on each sample.
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2

Characterization of Standardized PEA-LNPs

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The morphology of standardized PEA-LNPs was observed using scanning electron microscopy (SEM, Nova NanoSEM 450, Fei, Eindhoven, The Netherlands) with a TDL detector. Particle suspension was dropped on an aluminum stub, and after drying, coated with carbon under vacuum conditions (Carbon Coater, Balzers CED-010, Oerlikon Balzers, Balzers, Liechtenstein).
Size, polydispersity index (PDI), and surface charge (Z-potential) were measured by light scattering using Zetasizer PRO—Red Label (Malvern Panalytical, Worcs, UK) equipped with a 10 mW He-Ne laser (632.8 nm) and ZS Xplorer software (version n. 3.1.0.64).
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3

Determining Lipid Vesicle Zeta Potential

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Zeta potential (ζ)
measurements were performed with a Zetasizer Pro Red Label (Malvern).
LUVs were covesiculated with 5 μM of each AM at a total lipid
concentration of 1 mg/mL. About 600 μL of each LUV sample was
diluted to obtain a total lipid concentration of 0.25 mg/mL, with
phosphate buffer, 5.57 mM ionic strength, pH 7, 20 °C, and put
in a disposable folded capillary cell (polycarbonate, Malvern). Each
ζ potential value is the average of three independent runs;
for each temperature, the ζ potential was determined as the
mean of 5–8 measurements. The reported error is the standard
deviation of the measurements. The measurements were performed in
the range 10–60 °C, every 2 °C (except every 1 °C
in the range 38–50 °C for ENT-03 containing LUVs, to better
appreciate the transition). The electrophoretic mobility measurements
were converted into ζ values according to the Smoluchowsky model.41 The temperature was internally controlled (accuracy
±0.1 °C). The ζ potential measurements were also used
to determine the transition temperature (Tm) in LUV systems.42 (link) The Tm values were determined by analyzing the first-order
derivative of ζ with respect to temperature (dζ/dT) as a function of temperature: the Tm corresponds to the minimum of the curve, while the amplitude
of the transition was assumed to correspond to the full width at half
maximum (FWHM) of the derivative curves.
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