The amount of active substance released was determined using liquid chromatography using an Agilent liquid chromatograph with DAD-type UV-Vis detector. In order to determine the amount of active substance in the samples, calibration curves were made for gallic acid in the two simulated biological fluids (SGF and SIF) in areas of adequate concentrations relative to the theoretical concentrations of gallic acid.
Liquid chromatograph
A liquid chromatograph is an analytical instrument used to separate, identify, and quantify components in a liquid sample. It functions by passing the sample mixture through a column filled with a stationary phase, which interacts with the sample components, causing them to separate based on their physical and chemical properties.
5 protocols using liquid chromatograph
Gallic Acid Release from Mesoporous Silica
The amount of active substance released was determined using liquid chromatography using an Agilent liquid chromatograph with DAD-type UV-Vis detector. In order to determine the amount of active substance in the samples, calibration curves were made for gallic acid in the two simulated biological fluids (SGF and SIF) in areas of adequate concentrations relative to the theoretical concentrations of gallic acid.
Metabolite Profiling of Biological Samples
Methanol (Batch Number: 196063, Chromatography pure, Fisher Chemical, Shanghai, China), Acetonitrile (Batch Number: 201643, Chromatography pure, Fisher Chemical, United States), Formic acid (Batch Number: 171662, Chromatographic purity, Fisher Chemical, Shanghai, China), and Wahaha Purified Drinking Water (Hangzhou Wahaha Group Co., Ltd., Shanghai, China).
Molecular Weight Determination of PLA Composites
GPC Characterization of Polymer Scaffolds
HPLC Analysis of Bioactive Compounds
compounds were performed by HPLC on an Agilent Liquid Chromatograph,
equipped with a quaternary pump, an autosampler, a thermostatted column
compartment, and a UV-detector (205 and 296 nm), according to the
method described by Yuan et al. with some modifications.26 (link) The optimized chromatographic column was C18-00G-4375-E0
(250 mm × 4.6 mm; Phenomenex) and mobile phase was 90:10:0.001
(v/v/v) methanol/isopropanol/formic acid at a flow rate of 1 mL/min.
The column was kept at a constant temperature (30 °C), and 10
μL of the sample was injected in all of the analyses. The standard
curve was drawn for each compound and quantified by the external standard
method.
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