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158 protocols using zen3600

1

Zeta Potential and Particle Size Analysis

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The copolymers and microspheres were individually dispersed in a PBS buffer solution to create a 0.1 mg/mL solution. Zeta potential testing was carried out on these three sets of samples utilizing a laser particle size analyzer (ZEN 3600, Malvern Instruments Ltd., England, UK). Following this, the microspheres were dispersed in a PBS buffer solution to formulate a 0.1 mg/mL solution. Subsequently, the average particle size of the three microgel particles was determined using a laser particle size analyzer (ZEN 3600, Malvern Instruments Ltd., Malvern, UK).
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2

Particle size and zeta-potential analysis

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The determination of particle size and polydispersity index (PdI) of the NAR-NGE-NPs was performed in triplicate by dynamic light scattering (Zetasizer ® , model ZEN 3600, Malvern) after 500-fold dilution (v/v) in water. The zeta-potential was obtained by electrophoresis (Zetasizer ® , model ZEN 3600, Malvern), after 500-fold dilution (v/v) in NaCl 10 mM.
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3

Characterization of Curcumin Nanocapsules

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We used the dynamic light scattering technique to determine the mean particle size and polydispersity index (Zetasizer® nano-ZS model ZEN 3600, Malvern). The zeta potential (ZP) was determined using the electrophoretic mobility technique (Zetasizer® nano -ZS model ZEN 3600, Malvern) and pH was determined directly using a potentiometer (DM-22, Digimed®) [30] (link).
The curcumin content in the nanocapsules was determined using high-performance liquid chromatography (HPLC). The encapsulation e ciency was determined using ultra ltration-centrifugation with subsequent HPLC analysis according to the methodology described by Jaguezeski et al. [29] (link).
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4

Characterization of Curcumin Nanocapsules

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We used the dynamic light scattering technique to determine the mean particle size and polydispersity index (Zetasizer® nano-ZS model ZEN 3600, Malvern). The zeta potential (ZP) was determined using the electrophoretic mobility technique (Zetasizer® nano -ZS model ZEN 3600, Malvern) and pH was determined directly using a potentiometer (DM-22, Digimed®) [30] (link).
The curcumin content in the nanocapsules was determined using high-performance liquid chromatography (HPLC). The encapsulation e ciency was determined using ultra ltration-centrifugation with subsequent HPLC analysis according to the methodology described by Jaguezeski et al. [29] (link).
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5

Droplet Size and Excipient Impact on SEDDS/SNEDDS Performance

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The droplet size of the self-emulsifying formulations and the use of excipients in formulation is a crucial factor to its performance by which the rate and extent of drug release as well as absorption can be estimated (Gursoy and Benita, 2004 (link)). The droplet size, PDI and zeta potential of the diluted LFCS Types I, III, and IV SEDDS/SNEDDS were measured by laser diffraction analysis using Zetasizer particle sizing systems (Model ZEN3600, Malvern Zetasizer nano series, United Kingdom). The formulations were diluted freshly at a ratio of 1:1000 w/v (SEDDS/SNEDDS: distilled water) and mixed for 1 min before analysis. The cuvette was used to fill diluted samples in the sample compartment and the data were collected for 10 times. All experiments were carried out in triplicates and represented as mean ± standard deviation.
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6

Comprehensive Characterization of Prepared Samples

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Crystallinity and phase purity of the prepared samples were investigated by the powder X-ray diffraction (XRD, Philips, X-pert) with the Cu-K α radiation and a Ni filter (λ = 0.15418 nm). Fourier Transform Infrared (FTIR) spectroscopy analysis was carried out on a Bruker Vertex 70 spectrometer in the range of 4000-400 cm−1. The morphology and particle size of the samples were observed by a Transmission Electron Microscopy (TEM) with an acceleration voltage of 120 kV. The magnetic properties of the samples were measured by a vibrating sample magnetometer (VSM, Meghnatis Kavir Kashan Co., Iran) instrument at room temperature. The hydrodynamic size distribution of the prepared sample was measured by dynamic light scattering (DLS, Malvern zeta sizer-ZEN3600).
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7

Measuring Solid-Liquid Interface Charges

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To assess the electrostatic stability and charges behavior in the solid-liquid interface of tested materials we analyzed the zero point of charge (pHpzc). Briefly, solutions containing water and 100 mg of the tested material were prepared at different pH conditions (2, 4, 4.5, 6, 7 and 9). Samples were vortexed for 1 min, and centrifuged at 5000 rpm. To measure ζ we used a Zetasizer equipment (Nano ZS; Malvern Zetasizer ZEN3600, Worcestershire, UK). While ζ is the potential difference between the dispersion medium and the stationary layer of the fluid, the point of zero charge (PZC) is the pH at which the overall charge of the particles is zero [64 ]. Analyses were conducted in triplicate. Data are presented as mean values (mean ± SD).
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8

Characterization of Silver Nanoparticles

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The silver ion reduction was observed by various wavelengths from 200 to 1000 nm by measuring double-beam UV–Vis spectra (model Victoria, Australia) (Al-Zaban et al., 2019a (link)). The size and shape of AgNPs were performed using transmission electron microscopy (Al-Othman et al., 2017 ) (JEM 1400 plus model with an acceleration voltage of 100 kV). ZETA Seizers (Malvern Zetasizer ZEN 3600, UK) was used to determine the distribution size of AgNPs of the colloidal solution (Abd El-Aziz and Al-Othman 2019 ). AgNPs were freeze-dried using a Heto Lyophilizer (Heto-Holten, Denmark) for XRD measurements, then the powdered sample was analyzed by an X'pert PRO PANalytical diffractometer using CuKpha radiation (k = 1.54056 Å) in the range of 20 ≤ 2ɵ ≤ 80 ≤ at 40 keV (Al-Othman et al., 2017 ). The FTIR a Nicolet 6700 spectrometer (Thermo Electron Corporation, USA) was confirmed functional biomolecules, the region spectrum in the 400–4000 cm−1 (Abd El-Aziz, 2014 ).
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9

Vesicle Size Determination by Extrusion

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The elasticity of SNVs was studied by extrusion at a pressure of 2.5 bars and a pore size of 100 nm within a nylon membrane filter for three minutes. Using Zetasizer (ZEN 3600, Malvern Instruments Limited, UK), the vesicle size of various formulae, before and after filtration was determined. Using the following equation (Shoman et al., 2023 (link)):
DI=Jrv/rp2
where J is the amount of the extruded formulation, rv: the vesicle size of the formulation (after extrusion) and rp: the pore size of the nylon membrane filter.
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10

Particle Size Analysis of Aqueous Samples

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After each sample was prepared into a 1 mg/mL solution with water, the Laser particle size analyzer (ZEN3600, Malvern Instruments Ltd., U.K.) was used to measure the hydrodynamic radius. The measuring temperature was 25 °C and the scattering angle was 173°.
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