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14 protocols using v 550 uv vis

1

Characterization and Photocatalytic Activity of Ag-doped and Ag-core TiO2

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The morphologies of Ag-doped TiO2 and Ag-core TiO2 were observed using transmission electron microscopy (TEM; JEM-2100, JEOL, Tokyo, Japan). Absorption spectra of Ag-doped TiO2 and Ag-core TiO2 were recorded using an ultraviolet–visible spectrophotometer (V-550 UV/VIS, JASCO, Tokyo, Japan). X-ray diffraction was conducted using an X-ray diffractometer (XPert Powder, PANalytical B.V. Netherlands). An energy dispersive spectrometer was used to observe the distribution pattern of various elements (Ag, Ti, and O) using TEM-EDS (JEM-2100 Plus, JEOL Ltd., Japan), operating with an accelerating voltage of 200 kV. The photocatalytic capability of Ag-doped TiO2 (1%, 2%, 3%, and 4%) and Ag-core TiO2 (5 nm, 10 nm, 15 nm, and 20 nm) were evaluated through the photocatalytic degradation of methylene blue under a simulated sunlight Xenon lamp with an emission spectral range of 380 nm to 700 nm. The irradiation time was 10 min at 665 nm. The absorption intensity was recorded using an ultraviolet–visible spectrophotometer (V-550 UV/VIS, JASCO, Tokyo, Japan).
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2

UV/Vis Spectrophotometric Characterization

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The UV/Vis measurements were done using a JASCO V-550 UV/Vis (JASCO International Co. Ltd, Sapporo, Japan) spectrophotometer in the wavenumber range 300–600 nm, using a tungsten lamp and a 0.1 nm resolution, operating in the absorption mode.
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3

Comprehensive Analytical Characterization

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NMR, UV, and IR spectra were obtained using Bruker AV-600 (Bruker; Ettlingen, Germany), JASCO V-550 UV-VIS (Jasco; Tokyo, Japan), and JASCO FT/IR-480 plus FT-IR spectrometers (Jasco; Tokyo, Japan), respectively. LC-QTOF-MS data were generated using a Shimadzu LC-20AD liquid chromatogram (Shimadzu; Kyoto, Japan) and an AB SCIEX X500R QTOF mass spectrometer (AB SCIEX; Framingham, MA, USA). The MTT reagent was obtained from Keygen Biotech located in Nanjing, China. The PI reagent was obtained from Sigma-Aldrich®, (St. Louis, MO, USA). The RNase A reagent was procured from Fermentas® (Shanghai, China). Detailed instruments and chemicals are provided in the Supporting Information.
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4

Morphological and Optical Characterization of AlPcS4 Conjugates

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The morphologies of AuNR–AlPcS4, Clip–AlPcS4, and F127–AlPcS4 were observed using transmission electron microscopy (TEM; JEM-2100, JEOL, Tokyo, Japan). Dynamic light scattering (DLS) of Clip, Clip–AlPcS4, F127, and F127–AlPcS4 were measured using a Malvern Zetasizer Nano ZS (ZS90, Malvern Instruments Ltd, Malvern, UK). The fluorescence spectra (including fluorescence excitation spectra and fluorescence emission spectra) of AuNR–AlPcS4 with or without 808 nm laser irradiation, Clip–AlPcS4, F127–AlPcS4, and free AlPcS4 were measured by a fluorescence spectrophotometer (F-4500, HITACHI, Tokyo, Japan). Zeta potentials of AuNR, AuNR–AlPcS4, Clip, Clip–AlPcS4, F127, and F127–AlPcS4 were observed using the same Malvern Zetasizer Nano ZS. Absorption spectra and stability of AuNR–AlPcS4, Clip–AlPcS4, and F127–AlPcS4 were recorded using an ultraviolet–visible spectrophotometer (V-550 UV/VIS, JASCO, Tokyo, Japan).
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5

Analytical and Preparative HPLC Characterization

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Analytical HPLC was performed on an Agilent 1200 with an Agilent DAD spectrophotometer (Agilent Technologies, Santa Clara, USA) and a YMC-Pack Pro C18 (5 μm, 4.6 × 250 mm, YMC Ltd., Japan). Preparative HPLC was performed on a Shimadzu LC-20A spectrophotometer and a YMC-Pack Pro C18 column (5 μm, 20 × 250 mm). NMR (1D and 2D) spectra were recorded by a Bruker AVANCE III 600 spectrometer. The ESI-MS spectra were measured on a 6430 Triple Quad mass spectrometer (Agilent Technologies, Santa Clara, USA). The HR-ESI-MS spectra were recorded using a Q-TOF mass spectrometer (Waters Corporation, Milford, USA). UV and IR data were measured using a JASCO V-550 UV/vis and a JASCO FT/IR-480 plus spectrometers (Jasco, Japan), respectively. Normal phase silica-gel (200–300 mesh) was purchased from Qingdao Haiyang Chemical Co., Ltd., Octadecylsilanized silica (ODS) gel (50 μm) was purchased from YMC Ltd. in Japan. The optical density was measured on a Tecan Infinite®200 PRO microplate reader (Tecan, Swiss).
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6

Characterization of Gold Nanoparticles

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The absorption spectra of the AuS and PEG-AuS were measured by ultraviolet-visible spectrophotometer (V-550 UV/VIS, JASCO, Tokyo, Japan). The AuS and PEG-AuS morphologies were obtained using transmission electron microscopy (TEM) (JEM-2100, JEOL, Tokyo, Japan). Dynamic light scattering (DLS) and the zeta potential of AuS and PEG-AuS were observed with a Malvern Zetasizer Nano ZS (ZS90, Malvern, UK).
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7

Spectroscopy of AlPcS4 with Anti-Cancer Drugs

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The absorption spectra of free-AlPcS4 (8 µg/ml), AlPcS4 (8 µg/ml) in the presence of 5-FU (20 µM), DOX (0.4 µg/ml), CDDP (5 µM), MMC (0.5 µg/ml) and VCR (0.1 µg/ml) were assessed at 1-h intervals for 6 h by an ultraviolet-visible spectrophotometer (V-550 UV/VIS; Jasco International, Co., Ltd., Tokyo, Japan). Fluorescence spectra of free-AlPcS4, AlPcS4 in the presence of 5-FU, DOX, CDDP, MMC, and VCR were recorded using a fluorescence spectrophotometer (F-4500; Hitachi, Ltd., Tokyo, Japan).
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8

Extinction Spectra of Aqueous Samples

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Extinction spectra were collected by means of a double beam spectrophotometer Jasco V-550 UV/VIS equipped with quartz cuvettes of 1.5 mm path length and normalized to the maximum absorbance. MilliQ water was employed as solvent.
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9

Comparative Analysis of SPE Adsorbents

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Twenty-five compounds were analyzed by the UV-vis spectrometer to compare SPE capability using either Starbon A800, C18, or PGC adsorbents. The calibration curves of each analyte were plotted through five points: 1, 5, 10, 18, and 25 ppm. Then the spectra were measured under the scanning mode of Jasco V-550 UV-vis, the highest peak and corresponding identifying UV wavelengths were determined based on each spectrum. Based on each calibration graph, the linearity coefficient (R2) and the coefficient equation were calculated, and the measured UV-absorbance intensity of each sample could be converted into the concentration of each selected compound. Quantitative analysis of each compound from the solid phase extraction (Starbon A800, C18, and PGC) was calculated based on the slopes of the calibration curves. The results are the mean of the three experiments (N = 3).
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10

Characterization of Au@TiO2 Nanostructures

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The spectra of HMME, Au nanoparticles, Au@TiO2 core-shell nanostructures and Au@TiO2–HMME were measured and compared by ultraviolet-visible spectrophotometer (V-550 UV/VIS, JASCO, Ashikaga, Japan).
The morphological characteristics and dispersion of different nanostructures, such as, gold nanospheres, AuNP@TiO2 with different size, AuNR@TiO2 with different SPRL and the Au@TiO2–HMME conjugate, were observed by transmission electron microscopy (TEM) (H-600 TEM, NEC, Tokyo, Japan) The nanomeasure software was used to measure the statistical size of gold nanoparticles. The particle size and surface potential of nanomaterials were measured and analyzed by a laser particle size analyzer (Mastersizer 2000, Malvern, Malvern, UK).
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