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27 protocols using lb 550

1

UV-Vis and DLS Characterization of Particles

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UV–vis spectra
were collected in the wavelength range of 200–700 nm with a
PerkinElmer Lambda 365 UV–vis spectrometer at 25 °C, with
quartz cuvettes (0.1 cm optical path), with a spectral resolution
of 1 nm. The particle hydrodynamic size analysis was performed using
a DLS (Horiba LB-550) instrument. Results are presented as means ±
standard deviation (SD) of at least three measurements.
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2

Characterization of OTN-PNP Nanoparticles

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The
sizes of the OTN-PNPs
were determined using dynamic light scattering (LB-550, Horiba, Japan).
The absorption spectra of the NP samples were measured using an ultraviolet–visible-NIR
(UV–vis-NIR) spectrophotometer (V-770, JASCO, Japan). The fluorescence
emission spectra of the OTN-PNP samples were measured under excitation
with 980 nm light obtained from a xenon lamp set at 450 W in a spectrofluorometer
(Fluorolog-3-21-NIR, Horiba, Japan) and a spectrometer (NIR-256-1.7;
Avantes, Apeldoorn, Netherlands) equipped with a fiber-coupled diode
(SP-976-5-1015-7; Laser Components GmbH, Olching, Germany) as the
980 nm excitation source.
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3

MWCNT Dispersion Characterization in Cell Culture

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Sample-A and Sample-B were produced by Showa Denko K.K. (Tokyo, Japan) and Hodogaya Chemical Co., Ltd. (Tokyo, Japan), respectively. The MWCNTs were dispersed in 0.5% Pluronic F-68 (Sigma-Aldrich, St. Louis, MO, USA) at the concentration of 1 mg/mL. Stock solutions were sonicated for 30 min before being diluted in culture medium and applied to HL-60 cells. Hydrodynamic diameter of the MWCNTs in the culture medium was determined with a dynamic light scattering nanoparticle size analyzer (LB-550; HORIBA Ltd, Kyoto, Japan) at 25.0 °C ± 0.1 °C. The light source was a 650-nm laser diode of 5 mW.
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4

Liposome Size Characterization by DLS

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Liposome preparations’ hydrodynamic radius at 25 °C was obtained by DLS (Nanoparticle Size Analyzer, Horiba Jobin Yvonne LB-550, Horiba Jobin Yvon SRL, Opera Milano, Italy), with 100 samplings per measurement. The power spectrum (PS) obtained by fast Fourier transformation of the light intensity fluctuations was converted into particle size distribution by comparing it, using the Twomey method [27 (link)], with the calculated frequency distribution based on the Brownian movement for particles of different size.
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5

Liposomal Size Distribution and Stability

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The particle size distribution of liposomes was determined using a dynamic light scattering instrument (LB-550, Horiba Ltd., Kyoto, Japan). Liposomal dispersions were diluted with double-distilled water to ensure the light scattering intensity in the instrument’s sensitivity range. The stability of the liposomal formulations was evaluated after storage at 4 °C for 1, 7 and 14 days. All measurements were taken in triplicate.
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6

UV-Vis Characterization of AuNPs

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UV-vis spectroscopy was performed on the aqueous dispersions of AuNPs, in quartz cuvettes with 1 and 0.1 cm optical path length, in the wavelength range 200–700 nm, at 25 °C, with a spectral resolution of 1 nm on a Perkin Elmer UV-vis spectrometer (Lambda 2S, Waltham, MA, USA). Samples were pre-equilibrated prior to the initial scan for 2 min at RT. Particle size analysis was performed by dynamic light scattering (Horiba LB-550, Kyoto, Japan) and the results were presented as the mean of at least three measurements.
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7

Bismuth Nanoparticle Characterization

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DLS
measurements were performed on a Horiba LB-550 dynamic light scattering
instrument and an instrumental algorithm was used to supply the hydrodynamic
diameters as number distributions. For these measurements, freshly
syringed filtered samples were dispersed in water and measured at
five dilutions to ensure size distributions independent of concentration
effects. To determine the core loading (i.e., the volume percent bismuth),
the same sample used to determine BiNP core size by TEM (synthesized
at 80 °C with glucose surfactant) was also measured by both SEM
and DLS.
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8

NaYF4 Nanoparticle Characterization

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The particle size distribution and morphology of the NaYF4 NPs were evaluated via TEM (HD-2300, Hitachi, Japan) with accelerating voltage of 200 kV. The crystalline phase of the NaYF4 NPs was evaluated via XRD (RINT-TTR III, Rigaku, Japan). The hydrodynamic diameters of the NaYF4 NPs samples (solvent: cyclohexane, concentration: 2 mg/mL, room temperature) were determined using a dynamic light scattering particle size analyzer (LB-550; Horiba, Ltd., Kyoto, Japan).
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9

Nanoparticle Size and Zeta Potential Analysis

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Particle size measurements and size distribution of the composite nanoparticles were studied by dynamic light scattering technique (DLS) using a dynamic light scattering particle size analyzer Horiba LB-550 apparatus equipped with a diode laser with a wavelength of 650 nm and working at an angle of 90° and temperature 25 °C. The analysis was performed right after the preparation of the nanoparticle dispersions according to Ali et al.48 (link). The zeta potential and size distribution of nano-TiO2 before and after modification were determined by the DLS method by using an SZ-100 Zetasizer (Malvern). Before, the samples were dispersed in distilled water according to Nguyen et al.49 (link).
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10

Liposomal Particle Characterization and Stability

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The particle size distribution of liposomes was determined using a dynamic light scattering instrument (LB-550; HORIBA Ltd., Kyoto, Japan). Liposomal dispersions were diluted with double-distilled water to ensure the light scattering intensity in the instrument’s sensitivity range. The particle stability of the Cur- or BDMC-loaded liposomes (Cur-Lip and BDMC-Lip) was evaluated after storage at 4°C for 14 days and incubation with DMEM containing 10% bovine serum albumin at 37°C for 7 days. The measurements were performed in triplicate.
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