The largest database of trusted experimental protocols

19 protocols using uv 1601 uv visible spectrophotometer

1

Quantifying Polyphenols in Rocket Leaves

Check if the same lab product or an alternative is used in the 5 most similar protocols
The total polyphenol content (TPC) of rocket leaves was determined by the Folin-Ciocalteu method reported by Toledo-Martín et al. [36 (link)], with modifications. Briefly, 400 mg of lyophilized rocket leaves was added to 8 mL of ethanol (with 1% hydrochloric acid) and shaken for 30 s and centrifuged at 4000× g for 15 min. To 180 μL of the supernatant, 300 μL of Folin-Ciocalteu reagent, 4800 μL of deionized H2O, and 900 μL of a 20% Na2CO3 solution in water (w/v) were added. After incubation for 60 min in the dark at room temperature, the absorbance was read at 765 nm using a UV-1601 UV-Visible spectrophotometer (Shimadzu, Milan, Italy). A calibration curve (R2 = 0.99) was constructed with gallic acid at different concentrations (25, 50, 100, 150, 200 mg/L). The results were expressed as mg of gallic acid equivalent (GAE)/100 g of dry weight (mg GAE/100 g D.W.).
+ Open protocol
+ Expand
2

Synthesis and Characterization of CdTe QDs

Check if the same lab product or an alternative is used in the 5 most similar protocols
Thioglycolic acid stabilised cadmium telluride (CdTe) QDs were synthesised via the aqueous synthesis route, and characterised, by the Prof. Gun'ko Research Group (School of Chemistry, Trinity College Dublin, Ireland) using published procedures (Gaponik et al., 2002; Maguire et al., 2014). Aluminium telluride was purchased from Cerac Inc. (Wisconsin, USA), and all other chemicals for synthesis were purchased from Sigma‐Aldrich (Dublin, Ireland).
In this study, 3.2 and 3.6 nm QDs were utilised, and their physiochemical properties are detailed below in Table 1. A Shimadzu UV‐1601 UV‐Visible Spectrophotometer was used to measure QD absorption, with scans carried out in the 300–700 nm range. A Varian‐Cary Eclipse Fluorescence Spectrophotometer was used to determine the fluorescence emission/photoluminescence spectra of QDs. The excitation wavelength was 480 nm, and the emission was detected in the range 490–700 nm, with the quantum yields being calculated from the photoluminescence spectra using Rhodamine 6G as a reference. Zeta potential measurements were carried out using a Malvern Zetasizer Nano Series V5.10. Five measurements were usually taken for each sample, each made of 10 to 20 accumulations as optimised by the machine. QD sizes were determined using their UV absorbance spectra using previously published methodology (Yu et al., 2003).
+ Open protocol
+ Expand
3

Characterization of ZnO Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
The initial step of the synthesized NPs is the recognition of their structure, properties, and reaction mechanism. For this, different characterization techniques have been used. The absorption spectrum in the UV–Visible range of the fabricated ZnO-NPs was recorded using a Shimadzu UV-1601 UV–visible spectrophotometer. The surface morphology and particle size were established using Tescan Maia 3 scanning electron microscopy (SEM). The sample was characterized using a Shimadzu X-ray diffractometer (XRD-6000) using Cu-Ka radiation as a source of X-rays with a wavelength of K = 1.541 A° to determine the crystallinity of ZnO-NPs. The capping agents of ZnO-NPs were identified using Fourier transform infrared spectroscopy (FTIR) of IR Prestige-21, Shimadzu.
+ Open protocol
+ Expand
4

UV-Visible Absorption Spectroscopy

Check if the same lab product or an alternative is used in the 5 most similar protocols
Absorption spectra were gathered using a Shimadzu UV-1601 UV-Visible Spectrophotometer.
+ Open protocol
+ Expand
5

Uremic Toxin Characterization in ESRD

Check if the same lab product or an alternative is used in the 5 most similar protocols
Urea, creatinine and uric acid, the uremic toxins, present at the highest concentration in the blood of patients with end stage renal disease, were considered in this research. They are classified as soluble compounds with low molecular weight, MW < 500 Da, and as non-protein-bound toxins. For each of them, we used, as operative limits, the value of concentration present in the blood of healthy individuals, cN, and the highest concentration possible in hyperuricemia conditions, cMAX. The characteristics of the toxins are listed in Table 1. The toxin concentration was measured with UV readings at 200 nm for urea, at 235 nm for creatinine and at 290 nm for uric acid using a Shimadzu UV-1601 UV-Visible spectrophotometer.
+ Open protocol
+ Expand
6

Antioxidant Capacity Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
The chemicals gallic acid, 4-aminoantipyrine and horse
radish peroxidase (HRP) were purchased from Sigma Chemicals Co. (P.O. Box
14508, St. Louis, MO 63178, USA). l-Ascorbic
acid and hydrogen peroxide were purchased from BDH Chemicals (BDH Chemicals
Ltd Poole, England). Tannic acid was purchased from Riedel De Haen Ag,
Wunstorfer Strasse 40, SEELZE1, D3016, Germany. Phenol was purchased from
Fluka (Fluka chemie GmbH, CH-9471, Buchs, Switzerland). Plant extracts were
freeze dried using LFT 600EC freeze dryer. SHIMADZU UV 1601 UV Visible
spectrophotometer (Shimadzu Corporation, Kyoto, Japan) was used to measure
the absorbance.
+ Open protocol
+ Expand
7

Characterization of Synthesized Fe3O4 Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
The phase of as-synthesized Fe3O4 NPs was characterized by X-ray powder diffraction on a Bruker D8 Advanced Diffractometer System (Bruker AXS, Inc., Madison, WI, USA) equipped with Cu/Kα radiation in the 2θ range from 20° to 80° (λ = 1.5418 Å). The size and morphology of samples were characterized using a JEOL 100CX transmission electron microscope (TEM; JEOL Ltd., Akishima-shi, Japan). The mean particle size was obtained from TEM images by counting more than 100 particles. The structure of the particles was characterized using a high-resolution TEM (HRTEM) and selected area electron diffraction (SAED) on a JEOL100CX TEM. Dynamic light scattering (DLS) measurements were performed in a Malvern Zetasizer Nano-ZS device (Malvern, WR, UK) to determine the hydrodynamic size of Fe3O4 NPs before and after coating HLC in a colloidal suspension. The zeta-potential of the suspensions was measured at 25°C. UV-vis absorption spectra were taken using a Shimadzu UV-1601 UV-visible spectrophotometer (Shimadzu, Kyoto, Japan). Magnetic properties of the samples were characterized by a LakeShore Model 7407 vibrating sample magnetometer (VSM; Lake Shore Cryotonics Inc., Wersterville, OH, USA).
+ Open protocol
+ Expand
8

UV-Vis Absorbance of G05-4548 in PBS

Check if the same lab product or an alternative is used in the 5 most similar protocols
UV-visual absorbance of G05–4548 was obtained using a UV-1601 UV-Visible spectrophotometer (Shimadzu Corp.) equipped with 1.0-cm quartz cells. The PBS buffer at baseline was calibrated before experiments. The spectrum of 4 μmol/L G05–4548 was collected from 250 to 500 nm in PBS buffer.
+ Open protocol
+ Expand
9

Cytotoxicity and Antioxidant Evaluation Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Chemicals – Folin ciocalteu reagent, chemicals needed for cell culture and cytotoxicity studies were purchased from Sigma –Aldrich (P.O. box 14 508, St Louis, MO 63178 USA). 1-Diphenyl-2-picrylhydrazyl (DPPH), Triton X-100 solution (1%), gallic acid, sulfanilamide and ortho-phosphoric acid were purchased from Fluka (Fluka chemie GmbH, CH – 9471 Buchs). Tris base was purchased from Promega (Promega Corporation, Madison, WI 53711–5399, USA). All chemicals used were of analytical grade.
Shimadzu UV 1601 UV visible spectrophotometer (Shimadzu Corporation, Kyoto, Japan) was used to measure the absorbance. LFT 600 EC freeze dryer was used to obtain the freeze –dried residue of the AEFLL (LFT 600 EC, −90-95°C temperature, Hitachi pump with 10 valves). Cells were incubated at 37°C in a humidified CO2 incubator (SHEL LAB/Sheldon manufacturing Inc. Cornelius, OR 97113, USA). Olympus (1X70-S1F2) inverted fluorescence microscope (Olympus Optical Co. Ltd. Japan) for observation of cells and photographs were taken using a Nikon D700 camera (Nikon D700, Japan). Deionized water from LABCONCO (waterproplus) UV ultra filtered water system (LABCONCO Corporation, Kansas city, Missouri 64132–2696) or distilled water was used in all experiments.
+ Open protocol
+ Expand
10

UV-Visible Absorption Spectroscopy

Check if the same lab product or an alternative is used in the 5 most similar protocols
Absorption spectra were gathered using a Shimadzu UV-1601 UV-Visible Spectrophotometer.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!