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6 protocols using zetasizer nano zs size analyzer

1

Synthesis and Characterization of Lead Oxide Nanoparticles

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The suspension of lead oxide nanoparticles was prepared at the “Modern Nanotechnologies” Center for Shared Use of the Ural Federal University, Yekaterinburg, Russian Federation, by pulsed laser ablation of thin metal sheet targets of 99.99% pure lead in sterile deionized water as described elsewhere12 (link).
Scanning electron microscopy (SEM) and the particle size distribution function were used to establish and describe the particle shape and size. The average diameter of the suspended lead oxide nanoparticles equaled 49.6 ± 16 nm (Fig. 9).

Description of PbO nanoparticles used in the experiment: (a) a scanning transmission electron microscopy image of PbO nanoparticles in the suspension at 29,640 × magnification, and (b) the function of PbO nanoparticle size distribution.

The suspension stability was judged by the zeta potential value measured using the Zetasizer Nano ZS size analyzer (Malvern Panalytical, UK) and was high (zeta potential up to 42 mV, n = 3, deionized water), which enabled us to increase the particle concentration to 0.5 mg/mL by partial evaporation of water at 50 °C without changing the size and chemical identity of NPs.
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2

Synthesis and Characterization of AIE Dots

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All the chemicals were purchased from Aladdin (Beijing, China), J&K (Beijing, China) or Sigma-Aldrich (St. Louis, MO, USA), unless specifically stated. All the reagents were commercially available and of analytical reagent grade. The other solvents were purified by fractional distillation. Prior to use, all solvents were purified by fractional distillation. Deionized water with a resistivity of 18.2 MΩ·cm was used from a Milli-Q water purification system (Millipore Corp., Billerica, MA, USA). NMR spectra were recorded by Bruker Avance 300 (Bruker Corp., Rheinstetten, Germany). Mass spectra were recorded on an Agilent 1100 LC-MS system (Agilent Technologies Inc., Foster, CA, USA). The preparation process of AIE dots was completed by a bath sonicator (Bransonic, CPX2800H-C, Emerson Electric Co., Ferguson, MO, USA). UV-Vis absorption spectra were recorded using a UV-2550 UV-Vis spectrophotometer (Shimadzu Corp., Kyoto, Japan). Fluorescence spectra were measured by a Shimadzu RF-5301PC spectrophotometer (Shimadzu Corp., Kyoto, Japan). Transmission electron microscopy (TEM) images of the AIE dots were taken by JEM-2100F at 200 kV (JEOL, Ltd., Kyoto, Japan). DLS measurement was performed using a Malvern ZetasizerNano ZS size analyzer (Malvern Panalytical Ltd., Malvern, UK) at room temperature.
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3

Synthesis and Characterization of TB Nanoparticles

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TB was synthesized according to our previous work (Alifu et al., 2017 (link)). PS-PEG and other chemical regents which not specially mentioned were purchased from Sigma Inc., The deionized water (DI water, 18.2 MΩ cm resistivity) obtained from the system has been utilized in all the experiments Using a Shimadzu UV-3600 UV-vis spectrophotometer to measure UV-vis absorption spectra. Using a Malvern Zetasizer Nano ZS size analyzer to measure dynamic light scattering (DLS) and zeta potential at room temperature.
Fluorescence quantum yield was measured using a Hitachi F4500 spectrofluorophotometer. Rhodamine B (excitation wavelength: 365 nm) was used as a standard to determine the fluorescence quantum yields of the nanoparticles.
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Synthesis of Copper Oxide Nanoparticles

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The suspension of copper oxide nanoparticles was prepared at the Ural Federal University. We used pulsed laser ablation of thin metal sheet targets of 99.99% pure copper in sterile deionized water. The mean diameter of the suspended copper oxide nanoparticles was 21 ± 4 nm (Fig. 5), as shown by scanning electron microscopy (SEM). The suspension stability was judged by the zeta potential measured using the Zetasizer Nano ZS size analyzer (Malvern Panalytical, UK) and was found to be high (up to 42 mV, deionized water), enabling us to increase the particle concentration to 0.25 mg/mL by partial water evaporation at 50 °C without changing the size and chemical identity of nanoparticles.

(a) Suspended copper oxide nanoparticles (electron microscopy at 100,000 × magnification); (b) the particle diameter distribution function showing that the mean diameter of CuO NPs was 21 ± 4 nm.

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5

Characterization of Engineered Lipid Nanoparticles

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MSNs, MSNs@lip-1, and MSNs@lip-2 were characterized by the following analyses. Scanning electron microscopy (SEM, Quanta 200, FEI, Eindhoven, The Netherlands) and transmission electron microscopy (TEM, JEM-2100F, FEI, JEOL, Tokyo, Japan) were used to examine the morphology of the nanoparticles. Fourier transform infrared spectrum (FTIR) was recorded using a Nexus 670 Spectrometer (Thermo-Nicolet, Madison, WI, USA) with a wavelength of 400 cm−1–4000 cm−1. An X-ray photoelectron spectrum (XPS) was obtained using an Escalab 250 Xi spectrometer (Thermo Scientific, Waltham, MA, USA), and the binding energy was calibrated against the O1s peak at 523 eV. Thermogravimetric analysis (TGA) was conducted on a Q5000 instrument (TA Instruments, New Castle, DE, USA) at a heating rate of 10 °C/min from 25 °C to 800 °C. Hydrodynamic diameter and Zeta potential were measured by a dynamic light scattering technique (DLS) using a Zetasizer Nano ZS size analyzer (Malvern Instruments, Malvern, UK) equipped with a 633 nm He-Ne laser.
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6

Comprehensive Analytical Characterization of Molecular Probes

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The UV-absorption spectra of different probes were measured using a LAMBDA 1050+ spectrophotometer. The NIR-II fluorescence spectra of different probes were measured by Edinburgh instrument FLS920 fluorescence spectrophotometer. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was performed on different probes using an American BIO-RAD electrophoresis system. The covalent binding behavior of protein to different dyes was characterized by Orbitrap Eclipse high-resolution mass spectrometer. The binding behavior of L-Cysteine to different dyes was characterized by a high-resolution mass spectrometer (Agilent1290). The binding affinity between the HSA and 1080 chromophores was acquired through the ForteBio Octet Red96e molecular interaction analyzer (Biolayer interferometry technology, BLI). The particle sizes of different compounds were analyzed using a Malvern Zetasizer Nano ZS size analyzer. Transmission electron microscope (TEM) images were acquired through DTM-961002 of JEOL Ltd. The 1H-NMR spectra of all dyes were obtained on Bruker AVANCE III 400 MHz NMR spectrometers.
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