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5 protocols using uv 2450 spectrophotometer

1

Spectrophotometric Analysis of Salicylic Acid Inclusion Complexes

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The content of SA in the complex was calculated based on the method in [31 (link)]. Different concentrations of SA (0.03, 0.06, 0.09, 0.12, 0.15, 0.18, 0.21, and 0.24 mmol/L) with anhydrous ethanol as the solvent were measured using a Hitachi UV-2450 spectrophotometer. The absorbance was adjusted to 235 nm. The relationship between the concentration of SA and the absorbance was determined. The SA in the inclusion complex was extracted and diluted with anhydrous ethanol for spectrophotometric measurements. The encapsulation efficiency (EE) and loading capacity (LC) of the complexes were obtained according to: EE(%)=(Total       SA-Surface  SA) in the inclusion complexesTotal  SA×100%
LC(%)=(Total       SA-Surface  SA) in the inclusion complexesThe inclusion complexes×100%
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2

Characterization of Gadolinium-Doped Graphene Quantum Dots

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The morphology of the GQDs was subjected to examination using transmission electron microscopy (TEM, FEI Talos F200S, New York, NY, USA) and atomic force microscopy (AFM, (Bruker Daltonics Inc. Multimode 8.0, Massachusetts, MA, USA). The Fourier transform infrared (FT−IR) spectra, UV−Vis absorption spectra, and FL spectra were obtained through utilization of FT−IR spectrometer (FT-IR 6800 JASCO, Marseille, France), Shimadzu UV−2450 spectrophotometer, and Hitachi 7000 fluorescence spectrophotometer, respectively. The hydrodynamic (HD) size and zeta potential of the samples were measured through the utilization of a nano ZS90 analyzer (Malvern Instruments Ltd., Worcestershire, UK), with the measurements being conducted at room temperature. The concentration of Gd3+ within the Gd(DTPA)−GQDs was confirmed through the application of inductively coupled plasma mass spectrometry (ICP-MS, Agilent 720 ES, Santa Clara, CA, USA).
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Characterization of MoOx Quantum Dots

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A JEM-2010 TEM (JEOL Ltd, Japan) with a 200
kV accelerating voltage and an AFM in the ScanAsyst mode were used
to obtain the size and height of the MoOx QDs, whereas XPS (Thermo) was used to characterized the elemental
composition and bonding configuration. The fluorescence lifetime was
measured by an FL-TCSPC fluorescence spectrophotometer (Horiba Jobin
Yvon Inc., France). The absorption was measured using a Shimadzu UV-2450
spectrophotometer (Tokyo, Japan), whereas a Hitachi F-7000 fluorescence
spectrophotometer (Tokyo, Japan) or a USB-4000FL spectrophotometer
(Ocean Optical) was utilized to record the fluorescence spectra.
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4

Characterization of Novel Fluorescent Probe BPN-NBD

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All nuclear magnetic resonance (NMR) spectra of BPN-NBD were collected by a Bruker Avance 400 MHz spectrometer. A Zeiss LSM710 Wetzlar (German) laser scanning confocal microscope was used for fluorescence imaging. High-resolution mass spectrometry (HRMS) data of new compounds were tested on AB Sciex TripleTOF 4600. UV–vis absorption and fluorescence data were collected through a Shimadzu UV-2450 spectrophotometer and a HITACHI F-4600 fluorescence spectrophotometer, respectively. Ultra-high performance liquid chromatography (UHPLC) analyses were conducted on a Shimadzu NexeraX2 UHPLC LC-30A. Unless otherwise specified, all raw materials used for synthesis were purchased from the chemical suppliers in China and used directly without further refining.
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5

Comprehensive Characterization of Nanomaterials

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High-resolution transmission electron microscopy (HR-TEM) pictures were collected at 100 kV using a TECNAI G2 microscope (Thermo Fisher, Waltham, MA, USA). The image of scanning electron micrographs (SEM) was measured by a XL-30ESEM FEG scanning electron microscope (FEI, Hillsboro, OR, USA). FTIR spectra were conducted with a VERTEX 70 FT-IR spectrometer (Bruker, Bremen, Germany). The X-ray photoelectron spectroscopy (XPS) spectra were acquired using an ESCALAB 250Xi spectrometer (Thermo Fisher, Waltham, MA, USA). A Rigaku Minister apparatus was used to generate the X-ray diffraction (XRD) patterns (Tokyo, Japan). The UV absorption spectra were performed via a Hitachi UV2450 spectrophotometer (Tokyo, Japan). The fluorescence spectra were obtained using an F97Pro FL spectrophotometer coupled with a 1.0-cm quartz cell (Lengguang Technology, Shanghai, China). Additionally, the fluorescent, phosphorescent lifetime, and emission spectrum were analyzed at room temperature using an FLS-1000 fluorescence spectrophotometer (Edinburgh, UK).
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