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Zetasizer nano nano s

Manufactured by Malvern Panalytical
Sourced in United Kingdom

The Zetasizer Nano (Nano-S) is a laboratory instrument designed for particle and molecular size analysis. It utilizes dynamic light scattering technology to measure the hydrodynamic size of particles or molecules in the nanometer range.

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7 protocols using zetasizer nano nano s

1

Characterizing Nanoparticle Size by DLS

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Particle size was measured with a Zetasizer Nano (Nano-S) particle-size analyser from Malvern Instruments Ltd (UK). An aliquot of the dispersion of nanoMIPs in distilled water was sonicated for 15 min, vortexed for 30 min and then analysed by DLS at 25 °C in a 3 mL disposable polystyrene cuvette. Attenuator position, measurement duration and number of runs were automatically chosen by the instrument. The values are reported as an average of 6 measurements. The nanoMIP concentration was calculated from the absorbance intensity (at λ-198 nm), based on a previously obtained calibration curve.
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2

Nanoparticle Size Characterization by DLS

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Nanoparticle size was determined by DLS using a Zetasizer Nano (Nano-S) from Malvern Instruments Ltd. (Malvern, UK). Prior to DLS measurements samples were subjected to sonication and vortexing before filtering through a 1.2 μm glass fibre syringe filter. All measurements were performed at 25 °C.
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3

Nanoparticle Size Characterization by DLS

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To verify the size of the synthesized nanoparticles, the eluted fractions were analyzed using a Zetasizer Nano (Nano-S) from Malvern Instruments Ltd. (Malvern, UK). Solutions of nanoMIPs in water (1 mL) were sonicated for 10 min, filtered through glass fiber syringe filters (pore size 1.2 μm pore size) and analyzed by DLS at 25 °C in a 3 cm3 disposable polystyrene cuvette.
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4

Synthesis of Nanoparticle Molecularly Imprinted Polymers

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The polymerization mixture for the preparation of nanoMIPs comprised: NIPAM (39 mg), BIS (2 mg), TBAm (33 mg dissolved in 2 mL of ethanol), AA (2.23 μl for all templates except fumonisin B2) and NAPMA (2.2 mg only for fumonisin B2). The components were dissolved in water (100 mL), sonicated for 5 min, and degassed by bubbling with nitrogen for 30 min. Then 50 mL of this solution was added to 60 g of glass beads bearing the immobilized template. The polymerization was initiated by the addition of a solution (0.5 mL) of APS (60 mg/mL) containing TEMED (30 μL mL−1). The monomer mixture was allowed to polymerize at ambient temperature (20 °C) for 1.5 h. After this time, the beads were transferred into an SPE cartridge (60 ml) fitted with a 20 μm porosity PE frit. Unreacted monomers and other low affinity materials were removed by washing with double-distilled water (10 × 50 mL) at ambient temperature. Next, the temperature was raised to 60 °C and the fractions of high affinity nanoparticles were collected by washing with pre-warmed water at 60 °C (4 × 20 mL). The size of the nanoparticles was determined by dynamic light scattering (DLS) using a Zetasizer Nano (Nano-S) from Malvern Instruments Ltd (Malvern, UK).
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5

Nanoparticle Characterization Methods

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Ceramic beads with glass beads were agitated by a Retsch AS200 shaker (Retsch Inc.). A Zetasizer Nano (Nano-S) from Malvern Instruments Ltd. (Malvern, U.K.) was employed to determine the size of the nanoparticles by dynamic light scattering (DLS). SPR-4 sensor with its gold-coated sensor chips was supplied by Sierra Sensors (Germany). A transmission electron microscope (TEM) (Philips CM20, Philips Research) and a scanning electron microscope (SEM) (JEOL-JSM5800LV) were employed to characterize the MIPs nanoparticles.
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6

Characterization of Polymer Nanoparticles

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The size of all the nanoMIPs was determined by dynamic light scattering (DLS) using a Zetasizer Nano (Nano-S) from Malvern Instruments Ltd. (Malvern, UK). For further confirmation, nanoMIPs were also characterised using a Philips CM20 transmission electron microscope (TEM). Prior to DLS and TEM measurements, the solution of nanoMIPs was ultra-sonicated Please do not adjust margins Please do not adjust margins for 3 min to disrupt possible aggregates. To perform DLS, a small aliquot of nanoMIPs in water (1 mL) was tested. The dispersion was analysed by DLS at 25 °C in a 3 cm 3 disposable polystyrene cuvette. Attenuator position, measurement duration and number of runs were automatically chosen by the instrument. For TEM a drop of the nanoMIPs solution was placed on a carbon-coated copper grid and dried in a fume hood before measurement.
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7

Characterization of Polymeric Nanoparticles

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The particle size was measured with a Zetasizer Nano (Nano-S) particle-size analyser from Malvern Instruments Ltd (UK). An aliquot of the dispersion of nanoMIPs in distilled water was sonicated for 2 min and then analysed by DLS at 25 °C in a 3 cm 3 disposable polystyrene cuvette. The instrument automatically chose attenuator position, measurement duration and number of runs. The values are reported as an average of 4 measurements. Transmission Electron Microscopy (TEM) images of nanoMIPs were taken using a JEOL JEM 1010, 100 kV high contrast TEM equipped with a Gatan SC1000 Orius CCD camera (Gatan, Abingdon Oxon, UK). Samples for the analysis have been prepared by depositing a drop of the nanoMIPs dispersion, previously filtered through a 1.2 μm PES syringe filter, on a carbon-coated TEM copper grid (400 mesh), and leaving them to dry at room temperature. The nanoMIP concentration was assessed by freeze-drying an aliquot (20 ml) of the particle solution and then weighing the solid.
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