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Ultrospec 4300 pro uv visible spectrophotometer

Manufactured by Cytiva
Sourced in United Kingdom

The Ultrospec 4300 pro UV/visible spectrophotometer is a laboratory instrument designed for the quantitative analysis of chemical and biological samples. It measures the absorbance or transmittance of light through a sample over a range of ultraviolet and visible wavelengths, providing data on the sample's composition and concentration.

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4 protocols using ultrospec 4300 pro uv visible spectrophotometer

1

Synthesis and Characterization of CdTe Quantum Dots

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The water-soluble CdTe QDs were synthesized according to a previously reported method.31 (link) In brief, a freshly prepared NaHTe solution was mixed with a nitrogen-saturated Cd(NO3)2 solution at pH 11.2 (adjusted by dropwise addition of 1 M NaOH) in the presence of MPA as a stabilizing agent; the final concentrations of NaHTe, Cd(NO3)2, and MPA were 0.76, 1.74, and 2.55 mg mL−1, respectively. The CdTe precursor solution was heated in a water bath at 95 °C. Finally, the resulting CdTe QD solution was stored at 4 °C for future use. The photoluminescence spectrum of the CdTe QDs was recorded by using a fluorescence spectrophotometer (Hitachi F-4500, Tokyo, Japan), and the UV-vis absorption spectra of the CdTe QDs were obtained with an Amersham Pharmacia Ultrospec 4300 pro UV/visible spectrophotometer (England, UK). The size distribution and morphology of the prepared CdTe QDs were characterized by using a high-resolution transmission electron microscope (TEM, JEOL JEM 2100; Tokyo, Japan). The average hydrodynamic diameter and zeta-potential of the resulting CdTe QDs were determined with a particle size analyzer (Zeta Sizer Nano ZS90, Malvern Instruments Ltd, Worcestershire, UK). The fluorescence quantum yield (QY) of the synthetic CdTe QDs was determined using rhodamine 6G as a reference standard (QY = 95%) according to a previously described method.43 ,44
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2

Characterization of Graphene Oxide Nanoparticles

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The morphology and structure of the prepared GSPs were investigated using a JEOL JEM 2100 transmission electron microscope (TEM, Tokyo, Japan) and a Hitachi S-4800 scanning electron microscope (SEM, Tokyo, Japan). Dynamic light scattering (DLS) analysis was performed using a Zetasizer Nano-ZEN3700 instrument (Malvern, UK) to determine the size distribution of various GSPs. Ultraviolet-visible (UV-Vis) absorption spectra were obtained using an Amersham Pharmacia Ultrospec 4300 pro UV/visible spectrophotometer (England, UK). Fluorescence spectra were assessed with a Hitachi F-4500 fluorescence spectrophotometer (Tokyo, Japan). A commercial HG-8 strip reader was purchased from Shanghai Huguo Science Instrument Co., Ltd. (Shanghai, China).
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3

DPPH Radical Scavenging Assay for Antioxidant Evaluation

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Free radical scavenging activity was estimated as percentage inhibition of radicals. 2,2-Diphenyl-1-picrylhydrazyl (DPPH) is an artificially stabilized free radical [29 (link)]. An aliquot of diluted extract or gallic acid standard solution (5 mg/mL; ≥98% purity) was added to 1.7 mL DPPH methanolic solution (0.06 mM), mixed thoroughly, and kept in the dark for 20 min at room temperature. The mixture’s absorbance was examined at 517 nm using an Ultrospec 4300 Pro UV–visible spectrophotometer (Amersham Biosciences Corp. San Francisco, CA, USA). Blank was prepared using aqueous acetone (80%) mixed with the DPPH solution. The gallic acid standard curve (at ≥98% purity) was prepared, and the linearity of the gallic acid standard curve (r2 = 0.98) was obtained in the range of 20–80 μg/mL. The results were expressed as milligrams of gallic acid equivalents (GAE) per gram of fresh leaf (mg GAE/g fl). The following formula was used to calculate percentage inhibition [30 (link)]:
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4

Morphological Analysis of AIEMBs

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The morphology of the prepared AIEMBs was investigated using a JEOL JEM 2100 transmission electron microscope (TEM, Tokyo, Japan). The size distribution of various AIEMBs was analyzed via DLS, performed on a Zetasizer Nano-ZEN3700 instrument (Malvern, UK). UV-Vis absorption spectra were obtained using an Amersham Pharmacia Ultrospec 4300 pro UV/visible spectrophotometer (England, UK). Fluorescence intensity of AIEMBs was monitored using a Hitachi F-4500 fluorescence spectrophotometer (Tokyo, Japan). The ultrasonic homogenizer was supplied by Ningbo Scientz Biotechnology Co., Ltd. (Ningbo, China). The Bio-Dot XYZ3000 automatic dot film tester was supplied by BioDot (Irvine, CA). The automatic programmable cutter was purchased from Shanghai Jinbiao Biotechnology (Shanghai, China). The fluorescence reader (model number: FIC-Q1) was custom-made by Huguo Science Instrument Co., Ltd. (Shanghai, China). FB1 residues in real corn samples were confirmed by an LC-MS/MS instrument (Agilengt 1290-6538, Palo Alto, CA, USA).
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