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Zetasizer nano series

Manufactured by Malvern Panalytical
Sourced in United Kingdom, United States, Germany

The Zetasizer Nano Series is a dynamic light scattering (DLS) instrument used for the measurement of particle size, zeta potential, and molecular weight. It is capable of analyzing samples in the size range of 0.3 nanometers to 10 micrometers. The Zetasizer Nano Series provides accurate and reliable data on the physical properties of materials in liquid suspension or solution.

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316 protocols using zetasizer nano series

1

Dynamic Light Scattering Characterization of L-PDNPs

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DLS (Malvern-Zetasizer Nano ZS90)
was used to determine the average hydrodynamic diameter, Z-potential, and PDI of L-PDNPs; 100 μg/mL of L-PDNPs in Milli-Q
water was used for all the measurements using disposable polystyrene
cuvettes (Malvern Zetasizer Nano series) to measure the hydrodynamic
diameter and disposable folded capillary cells (Malvern Zetasizer
Nano series) for measuring surface Z-potential.
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2

Characterization of Functionalized PY-LCNPs

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Conjugation of TEMPO and PEG2000-NH2.HCl to the carboxylate group on the surface of the PY-LCNPs was confirmed by agarose (1%) gel electrophoresis under an applied voltage of 95 V for 30 min at room temperature in 1× tris-buffered saline (TBS). Particle size distribution and sample concentration were measured by dynamic light scattering (DLS) of LCNP solution (40× dilution of the original suspension) in water using a ZetaSizer NanoSeries equipped with a HeNe laser source (λ = 633 nm) (Malvern Instruments Ltd., Worcestershire, UK) and analyzed using Dispersion Technology Software (DTS, Malvern Instruments Ltd., Worcestershire, UK). Zeta-potential was measured on a ZetaSizer NanoSeries equipped with a HeNe laser source (λ = 633 nm) (Malvern Instruments Ltd., Worcestershire, UK) and an avalanche photodiode for detection. For each analysis, at least four measurements were performed, and the data were reported as average values ± standard error of the mean (SEM).
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3

Characterizing Extracellular Vesicle Size and Surface Charge

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Dynamic light scattering (DLS) measurements were carried out using ZetaSizer NanoSeries equipped with a HeNe laser source (λ = 633 nm) (Malvern Instruments Ltd, Worcestershire, UK) and analyzed using Dispersion Technology Software (DTS, Malvern Instruments Ltd, Worcestershire, UK). MVs were loaded into disposable cells, and data were collected at 25 °C. All the samples were prepared in 0.1 x PBS buffer pH 7.4. For each sample, the autocorrelation function was the average of five runs of 10 seconds each and then repeated about three to six times. CONTIN analysis was then used to number versus hydrodynamic size profiles for the dispersions studied.
For Zeta-Potential (ζ-potential) measurement, Laser Doppler Velocimetry (LDV) measurements were performed using a ZetaSizer NanoSeries equipped with a HeNe laser source (λ = 633 nm) (Malvern Instruments Ltd, Worcestershire, UK) and an avalanche photodiode for detection, controlled with DTS software. MVs were loaded into disposable cells, and data were collected at 25 °C. Three runs of the measurements were performed for each sample to achieve the zeta potential. All the samples were prepared in 0.1 × PBS buffer pH 7.4. For both DLS and zeta-potential, MVs were used at a 10-fold dilution from stock concentration.
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4

Characterizing Lipid-Based Nanoparticle Properties

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DLS (Malvern-Zetasizer Nano ZS90) was used to measure the average hydrodynamic diameter and the Z-potential of LMNVs and LMNVs associated with the protein corona (LMNV-PC). Briefly, 100 μg ml−1 of LMNVs were used to measure the average hydrodynamic diameter of the nanostructures using polystyrene cuvettes (Malvern Zetasizer Nano series), and to measure the Z-potential using disposable folded capillary cells (Malvern Zetasizer Nano series). To assess how PC affects the average hydrodynamic diameter and the Z-potential of the nanostructures, 100 μg ml−1 of LMNVs were dispersed in full serum for 1 min or 1 h and then washed three times by centrifugation at 16 000g for 5 min at RT (three passages). At the end of the washing steps, LMNV-PC complexes were re-suspended in Milli-Q water and the average hydrodynamic diameter and Z-potential were measured as previously described.
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5

Characterizing Lipid-Based Nanoparticle Properties

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DLS (Malvern-Zetasizer Nano ZS90) was used to measure the average hydrodynamic diameter and the Z-potential of LMNVs and LMNVs associated with the protein corona (LMNV-PC). Briefly, 100 μg ml−1 of LMNVs were used to measure the average hydrodynamic diameter of the nanostructures using polystyrene cuvettes (Malvern Zetasizer Nano series), and to measure the Z-potential using disposable folded capillary cells (Malvern Zetasizer Nano series). To assess how PC affects the average hydrodynamic diameter and the Z-potential of the nanostructures, 100 μg ml−1 of LMNVs were dispersed in full serum for 1 min or 1 h and then washed three times by centrifugation at 16 000g for 5 min at RT (three passages). At the end of the washing steps, LMNV-PC complexes were re-suspended in Milli-Q water and the average hydrodynamic diameter and Z-potential were measured as previously described.
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6

Dynamic Light Scattering Characterization

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DLS measurements were performed using a Malvern Zetasizer Nano Series running DTS software (4 mW, He-Ne laser, λ = 633 nm) and an avalanche photodiode (APD) detector. The scattered light was measured at an angle of 175° for DLS measurements. The temperature was stabilized to ±0.1 °C of the set temperature. All samples were prepared in Milli-Q water at the concentration of ~0.2 mg mL−1 of polymer and filtered through a 0.45 μm pore size filter to remove dust prior to measurement.
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7

Physicochemical Characterization of Nanocarriers

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The main physicochemical parameters of NCs, such as hydrodynamic diameter (DH), polydispersity index (PDI), and particle charge (ζ-potential), were analyzed by means of dynamic light scattering (DLS) and microelectrophoretic methods using Zetasizer Nano Series (Malvern Instruments, Worcestershire, UK) equipped with a He–Ne laser (632.8 nm). DLS measurements were conducted at 25 °C and the detection angle was 173°, as previously described [7 (link),21 (link),22 (link)]. Each value was an average of three runs, with at least 10–20 measurements. We applied the DTS (Nano) program for data evaluation.
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8

Nanoparticle Characterization Protocol

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The particle size, polydispersity indices, and zeta potential were determined using Zetasizer Nano Series (Malvern Instruments, Malvern, UK). The pH values were determined using a Digimed DM-20 calibrated potentiometer (Digimed, São Paulo, SP, Brazil). The encapsulation efficiency was determined by high-performance liquid chromatography as described by Giordani et al.13 (link)
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9

Nanoparticle Size Characterization by DLS

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The nanoparticle size distribution (hydrodynamic diameter) measurements were performed using Dynamic Light Scattering (Zetasizer Nano Series, Malvern Instruments). Each value was obtained as an average from three runs with at least 10 measurements. All measurements were performed at 25 °C in 0.015 M NaCl.
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10

Characterization of Nanoparticle Properties

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The size and zeta potential of the NPs were measured using dynamic light scattering (DLS) (Zetasizer Nanoseries; Malvern Panalytical Ltd, Malvern, Worcestershire, UK). All measurements were performed in triplicate at 25 °C. The fluorescence emission spectrum of VP (425 nm excitation) in various nanoformulations was measured in a spectrofluorometer (Cary Eclipse Spectrophotometer; Varian, Inc., Palo Alto, CA, USA) in a quartz cuvette at room temperature. The absorption spectra of different NPs were measured in a double-beam spectrophotometer (Cary UV–VIS–NIR; Agilent, Santa Clara, CA, USA) using 1 cm pathlength quartz cuvettes. The conjugation of TAT to the surface of the NPs was confirmed using both absorption and Fourier Transform InfraRed (FTIR) spectroscopy.
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