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35 protocols using uv 6100

1

Photocatalytic Degradation of Organic Pollutants

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Typically, the photocatalytic experiments were performed at room temperature as follows: 0.05 g of photocatalyst was added into 50 mL of MB solution (3 ppm). The solution was stirred in dark condition for 30 min to achieve the adsorption–desorption equilibrium. After that, the solution was irradiated under visible light for 30 min by fluorescent lamp and the sample was collected every 10 min. The collected sample was centrifuged at 10,000 rpm for 15 min to remove the photocatalyst from dye solution. Finally, the concentration of dye solution was measured by UV–vis spectrophotometer (UV-6100, Mapada) at the wavelength of 664 nm to determine the removal efficiency. Additionally, isopropyl alcohol, benzoquinone and ammonium oxalate was used as scavenger for the hydroxyl radical, super oxide, and hole respectively to determine main species during the photocatalytic process of MB.
Besides, the photocatalytic degradation of phenol was also conducted in this work. In which, 50 mL of 20 ppm phenol solution and a small amount of H2O2 (35%) was stirred with 1 g/L of photocatalyst and for 30 min under dark condition. Afterwards, the mixed solution was irradiated under visible light for 360 min. The sample was collected at every 120 min followed by centrifugation, and then measured at 270 nm spectrophotometer (UV-6100, Mapada) to determine the removal efficiency.
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2

Spectrophotometric Analysis of Thymol-Loaded Microparticles

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Lyophilized microparticles (5 mg) were completely dissolved in 10 mL DCM solutions under stirring. The amount of thymol was then measured spectrophotometrically (UV-6100S, Mapada, Shanghai, China) at 281 nm using a calibration curve. The calibration curve of thymol was linear in the range of 0–40 μg/mL with a high correlation coefficient (R2 = 0.99913). The encapsulation efficiency (EE) and loading capacity (LC) were calculated using the following formula:
EE = amount of thymol entrapped/initial amount of thymol × 100%
LC = amount of thymol entrapped/weight of microcapsules × 100%
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3

Chromium Adsorption by AL-TiNTs

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A total of 0.05 g of AL-TiNTs was added to the conical flask, which contains Cr(VI) solution (50 mg/L), and shaken well with a constant temperature shaker (150 rpm). The pH was adjusted with HCl and NaOH. Using a disposable syringe, the sample solution was aspirated at a fixed time in 2 mL and filtered. Cr(VI) was measured with UV-Vis spectrophotometer (UV6100s, MAPADA, Shanghai, China). Details of the parameters influencing the adsorption performance of AL-TiNTs are described in Text S8.
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4

Efficient IR783 Encapsulation in Nanoparticles

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The amount of the IR783 in IR783-NBs was determined by standard curve of UV–vis absorption spectra measured by a UV–vis spectrophotometer (Mapada UV-6100S, Shanghai, China). IR783-NBs was separated from the original solution by centrifugation of 1500 rpm for 5 min at 4°C. All the agents, IR783, DPPC, DSPE-PEG-Biotin, and IR783-NBs, were dissolved in ethyl alcohol. The encapsulation efficiency and loading rate of IR783 were calculated as follows:
EE%=weight of IR783 in IR783NBsweight of totaladdedIR783×100%,IR783loadingrate%=weight of IR783 in IR783NBsweight of IR783NBs×100%.
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5

Quantifying Malondialdehyde and Glycerol in Mycelia

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The content of malondialdehyde (MDA) was measured with a malondialdehyde content assay kit (BC0020, Solarbio Science & Technology Co. Beijing, China). The content of glycerol was measured as the method described previously (Lynch and Yang, 2004 (link)). In brief, 10 mg of lyophilized mycelia was dissolved in 4 mL of petroleum ether and 4 mL of 50% ethanol. This procedure was followed by vortexing for 5 min and centrifugation at 3,000 r/min for 10 min, 100 μL of the lower layer was mixed with 900 μL of 50% ethanol. Then, 1 mL of 0.015 mol/L KIO4 was added, and after incubation for 10 min, 2 mL of 5.5 mM/L L-rhamnose monohydrate and 4 mL of Nash reagent (150 g of ammonium acetate, 2 mL of acetic acid, and 2 mL of acetylacetone dissolved in distilled water to 1 L) was added. Lastly, the mixture was incubated in a water bath at 53°C for 15 min, and the absorbance of samples was measured with a UV/Vis spectrophotometer (UV-6100S, Mapada, Shanghai, China).
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6

Quantification of Serum Lipid Profiles

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Serum total cholesterol (TC), triglyceride (TG), LDL cholesterol (LDL-C), HDL cholesterol (HDL-C) were assayed by spectrophotometer (UV-6100s, Mapada, Shanghai, China) according to the kit’s instructions (Nanjing Jian cheng biotech, China). The content of TG and TC were measured at 510 nm, LDL-C and HDL-C were measured at 546 nm. The sensitivity of all kits: TC T-CHO Sensitivity: 0.01 mmol/l; TG T-CHO Sensitivity: 0.01 mmol/l; TG T-CHO Sensitivity: 0.01 mmol/l; LDL-C Absorbance difference ▲A of 0.180–0.280 for 2.6 mmol/l test subject; HDL-C Absorbance difference ▲A of 0.087–0.153 for 1.3 mmol/l test subject.
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7

Comprehensive Characterization of ZIF-8@GO Hybrid

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The morphology of
ZIF-8@GO was observed using TEM (JEM-2100, JEOL, Japan). XPS (PHI
5300, ULVAC-PHI, USA) was used to analyze the composition of ZIF-8@GO.
The XRD measurements were recorded on a diffractometer (D8 ADVANCE,
Bruker, Germany) using Cu Kα radiation (λ = 0.15418 nm)
at 40 kV and 40 mA. N2 isotherm adsorption at 77.5 K is
recorded on an ASAP 2020 BET surface analyzer (Micromeritics, America).
Prior to the adsorption measurements, the samples were outgassed at
80 °C for 5 h. UV–vis spectra of ZIF-8 and the ZIF-8@GO
hybrid were recorded on a spectrophotometer (UV-6100s, Mapada, China)
in the range of 200–800 nm. The SEM (S-4800, Hitachi, Japan)
with EDS was used to observe the surface morphology and composition
of the PLA/ZIF-8@GO fibrous membranes. The FT-IR spectra were obtained
using a spectrometer in the range of 400 to 4000 cm–1 (FT-IR-8400S, Shimadzu, Japan). Tensile testing was carried out
on a tensile tester (CMT, Sans, China) at a rate of 10 mm/min. The
samples were cut into strips of 0.5 cm × 4 cm. The values were
averaged over five measurements. The CAs were measured by a CA tester
geniometer (SL200B, Kino, USA). The membrane samples were measured
using the sessile drop method with water.
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8

Lipid Profile Quantification Protocol

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Serum total cholesterol (TC), triglyceride (TG), LDL cholesterol (LDL-C), HDL cholesterol (HDL-C) was assayed by spectrophotometer (UV-6100 s, Mapada, Shanghai, China) according to the kit’s instructions (Nanjing Jian cheng biotech, China). The content of TG and TC were measured at 510 nm, LDL-C and HDL-C were measured at 546 nm.
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9

Curcumin Quantification in Emulsions

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Dissolved 6 mg of CUR in 100 mL of absolute ethanol, diluted a part of the solution to a certain concentration (1, 2, 4, 8, 12, 16 µg/mL), and measured the absorbance at a wavelength of 425 nm using an ultraviolet spectrophotometer (UV-6100S, Mapada, Shanghai, China). For the standard curve of curcumin dissolved in ethanol (Figure S1).
Diluted the curcumin emulsion 100 times with absolute ethanol, measured the absorbance value, and calculated the curcumin content in the emulsion through the standard curve. Each sample was measured three times in parallel. Curcumin-load ratio was calculated using the following formula:
where C1 is the concentration of curcumin in the emulsion; C0 is the initial concentration of added curcumin.
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10

Controlled 5-FU Release from F127 and FL-2 Hydrogels

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F127 and FL-2 hydrogels with 20 wt% were used as carriers, and 5-FU was used as a model drug. Each group contained 2.0 g hydrogel and 5 mg 5-FU. The sample was not removed from the vial. They were then placed in 100 mL of phosphate buffer solution (PBS) and incubated at 37 °C. The absorbance of PBS was measured using an ultraviolet spectrophotometer (UV-6100s, MAPADA) at each fixed time interval. The corresponding concentration of 5-FU was calculated by the following equation: where A is the absorbance and c is the concentration. This equation calculates the cumulative release percentage (CR%). The in vitro drug release experiment was repeated five times, and the average values were obtained to plot the cumulative release curve.
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