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Folded capillary cell dts1060

Manufactured by Malvern Panalytical
Sourced in United Kingdom

The Folded Capillary Cell DTS1060 is a lab equipment product designed for dynamic light scattering (DLS) measurements. It is a specialized cell used in the characterization of particle size and molecular weight distributions of samples in solution. The core function of this product is to provide a controlled and reproducible environment for light scattering measurements.

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5 protocols using folded capillary cell dts1060

1

Particle Size and Zeta Potential Analysis

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The particle sizes and zeta potentials were determined by a Zetasizer Nano ZS at 20 °C. The instrument contains a 4 mW He-Ne laser operating at a wave length of 633 nm and incorporated noninvasive backscatter optics (NIBS). The measurements were performed at the detection angle of 173° and the software automatically determined the measurement position within the quartz cuvette. The 10 -3 -10 -5 M aqueous solutions of 2, vitD3 (dissolved in ethanol 1 × 10 -3 , 1 × 10 -2 and 1 × 10 -1 M) and vitD3 with macrocycle 2 complex were prepared. The concentration ratio of pillar[5]arene 2 and vitD3 in the complex was 1:1, 1:5, 1:10 and 2:1. Electrophoretic mobility of different samples was using a fold capillary cuvette (Folded Capillary Cell DTS1060, Malvern, U.K.). The experiments were carried out for each solution in triplicate.
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2

Nanoformulation Physical Characterization

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The physical characteristics of the NE formulations were assessed by DLS, Zeta potential measurement, and TEM. The hydrodynamic size was determined using a DLS device (Zetasizer Nano ZS; Malvern Instruments, Malvern, UK) and with the NEs diluted to 1:1000 (v/v) (mean of 3 independent measurements performed at 25 °C). The Zeta potential was measured using a Zetasizer Nano ZS device coupled to a Folded Capillary Cell (DTS1060) from Malvern Instruments. Oily droplets were quantified by NTA using a NanoSight NS300 instrument (Malvern Instruments). A Hitachi H7650 transmission electron microscope linked to an ORIUS SC1000 11MPX (Gatan Inc., Pleasanton, CA, USA) camera run by Digital Micrograph (Gatan Inc.) was used to study the NE samples (1:50 dilution, v/v) transferred to a carbon-coated copper grid. Iron concentration was quantified by UV spectrometry as previously described [66 (link)].
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3

Physicochemical Analysis of Nanoparticles

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Freshly prepared NP solutions were used for physicochemical analysis (Luo et al., 2010) (link). The mean particle size and PDI of the NP formulations were determined by dynamic light scattering (DLS). The ZP values were measured with the use of laser doppler velocimetry (LDV). Both DLS and LDV analysis were performed in triplicate at 25 °C with a Zetasizer Nano series Nano-ZS ZEN3600 fitted with a 633 nm laser (Malvern Instruments Ltd., UK), using a folded capillary cuvette (Folded capillary cell-DTS1060, Malvern, UK). The values presented herein were acquired from three separate experiments, each of which included three replicates; N=3.
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4

Chitosan-CNC Particle Characterization

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The electrophoretic mobility and z-average hydrodynamic diameter of chitosan–CNC PMC particles were measured by laser Doppler electrophoresis in a Malvern Zetasizer Nano ZS90 (Malvern Instruments, Inc., Westborough, MA, USA). Samples were prepared by mixing of a CNC suspension (0.02% (w/v)) and a chitosan solution (0.001% (w/v)), each with an ionic strength of 1 mM and a pH of 2.6, under strong agitation with a magnetic stir bar. The volumes of the two liquids were chosen to give sulfate/amino group molar ratio (S/N ratio) of 0.3. The obtained PMC particle suspensions were used without further dilution or filtration. Each measurement was performed at 25 °C in a Malvern DTS1060 folded capillary cell and was repeated two times.
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5

Zeta Potential Measurement of Dispersed Particles

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The ζ-potential of dispersions of particles (i.e. dispersed mucus, latex beads) was obtained from dynamic light scattering measurements at 37°C using a Nano-ZS Zetasizer (Malvern Instruments Ltd, Malvern, UK). Prior to analysis, ex vivo mucus samples (both, the non-treated controls and the DNase-treated) were gently dispersed in PBS buffer (pH 7.4) to give a concentration of ca. 0.1% w/v. The latex dispersions were diluted in PBS buffer to the concentration of ca. 0.001% w/v. Diluted dispersions were then injected into a DTS1060 folded capillary cell (Malvern Instruments Ltd). Each sample was analyzed at least 20 times and the results displayed as a mean. Data shown are the mean and standard deviation from three dispersions prepared under the same conditions.
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