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Nano flex

Manufactured by Microtrac
Sourced in United States, Germany

The NANO-flex is a laser diffraction particle size analyzer designed for the measurement of particle size distributions in the submicron range. It utilizes the principle of laser diffraction to determine the size distribution of particles suspended in a liquid or gas medium. The NANO-flex provides detailed information about the particle size characteristics without making any interpretations or extrapolations about the intended use of the equipment.

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5 protocols using nano flex

1

Colloidal Particle Size and Stability

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The hydrodynamic sizes of the particles in the colloidal samples and their stability were analyzed using dynamic light scattering (DLS) and ζ-potential measurements. The DLS measurements were performed using backscatter geometry with a 780 nm laser on a Nano-flex (Microtrac, Montgomeryville and York, PA, USA). For each sample, a set of five 2 min scans was collected. The ζ-potential data was collected using a Stabino (Particle Metrix GmbH, Ammersee, Germany).
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2

Comprehensive Characterization of Nanoparticles

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Particle size and distribution (poly-dispersity index, PDI) were determined by dynamic light scattering (DLS) using a Microtrac NANO-flex. Zeta potential of particle dispersion were measured by Stabino PMX 400. FTIR absorbance peaks were acquired using Bruker Tensor 27 FTIR spectrometer and NP dispersion and solution were dropped on KBr pellets and dried at 50 ºC. UV/Vis absorption spectra for F127 qualification was carried out with a UV–Vis–NIR spectrometer (Lambda 950, from Perkin Elmer). The photoluminescence spectra were measured using a JASCO spectrofluorometer FP-8500. SEM images were taken using a FEI Sirion SEM at 3 kV accelerating voltage. All samples were coated with 3 nm Pt before performing SEM measurements. AFM measurements were performed with a Nanosurf Easy Scan 2 in contact mode. Near-edge X-ray absorption fine structure (NEXAFS) spectroscopy have been recorded at the PolLux beamline at the Swiss Light Source66 (link). The samples were raster-scanned through the focal spot of a nickel zone plate with an outermost zone width of 25 nm (yielding approx. 30 nm lateral resolution) with a pixel resolution of 10 nm.
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3

Synthesis and Characterization of Titania Nanoparticles

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Titania nanoparticles were synthesized from TiBALDH (purchased from Sigma Aldrich, CAS No. 65104-06-5) through a simple precipitation method described in Seisenbaeva G. et al. 201319 (link) and from titanium tetraethoxide (CAS No. 3087-36-3) by the techniques of the Captigel patent no. WO07145573. The particles were washed by centrifugation at 4000 rpm three times in anhydrous ethanol and then washed in water four times. They were analysed by Thermo Gravimetric Analysis (TGA) in a Perkin-Elmer Pyris 1, X-Ray Powder Diffraction in Bruker SMART Apex-II multipurpose diffractometer operating with MoKα radiation λ = 0.71073, Energy-Dispersive X-ray Spectroscopy (EDS) and scanning electron microscopy (SEM) with an Hitachi TM-1000-μDeX. Transmission electron microscopy was used to determine the size of the particles using a Philips CM-20 Super Twin microscope, operating at 200 kV. The particle size in solution, both deionized water and M9-minimal salts, was investigated with nano tracking analysis with Nanosight 300 and additional investigation into the different aggregation-states of the particles analysed by dynamic light scattering (DLS) using Microtrac NANO-flex. The zeta potentials were measured on a Malvern Nano ZS.
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4

PLGA-NH2 Nanoparticle Characterization

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PLGA-NH2 NPs were analyzed for size, polydispersity index (PDI) and zeta potential, in the same way as in our previous study [31 (link)]. The NPs were dissolved at 0.1 mg/mL in MilliQ, and both size and PDI were measured by using a NANO-flex (Microtrac, Inc., Duesseldorf, Germany), and the data were analyzed by using Microtrac software (Microtrac FLEX 11.1.0.2, Duesseldorf, Germany). The zeta potential was measured by using Zetasizer Nano ZS (Malvern Instruments, Worcestershire, United Kingdom), where similar NP concentrations were dissolved in NaCl (5 mM, pH 7.4). Encapsulation efficiency of PFCE was measured by using a nuclear magnetic resonance (NMR, Bruker Avance III 400 MHz, Bruker BioSpin, Ettlingen, Germany) spectrometer coupled with a Broad Band Fluorine Observation (BBFO) probe. NPs, ~5 mg, were dissolved in 500 µL deuterium oxide (D2O) containing 100 µL 1 volume% trifluoroacetic acid (TFA) in D2O. For quantification, the interscan relaxation delay (D1) was set at 5 times the relaxation time (T1) of TFA, at 20 s. The data were evaluated with Mestrenova 10.0.2 (Mestrelab Research, Escandido, CA, USA).
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5

Wet Dispersion and DLS Analysis

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Samples for DLS were prepared as wet dispersion as described in the SEM section according to the method denoted ❷. After 60 min vortexing at 1250 rpm and sonication, the CeO2 sample was centrifuged for 36 s (short spin mode) at 100 g with a centrifuge (MiniSpin® plus, Eppendorf). Afterwards, 500 µL of the supernatant were carefully pipetted with a piston pipette (Eppendorf) into a new vial and measured. The ZnO-Isopropanol dispersion was left to sediment for 60 min before measurement. Here again, the supernatant was carefully taken from the sample and measured.
To determine the particle size of the dispersed powder samples (see sample preparation method ❷), DLS (NanoFlex, Microtrac) was applied according to ISO 22412:201712 . The instrument is operated in heterodyne mode with a wavelength of 780 nm under a measurement angle of 180°. The evaluation of the results was performed using frequency analysis utilizing the following refractive indexes: nwater = 1.33, nisopropanol = 1.39, nCeO2 = 2.42 and nZnO = 1.99. The refractive indices were used to obtain a volume-weighted particle size distribution by means of the Mie-correction.
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