The analysis of plasma concentrations of mycophenolic acid (MPA), the sole pharmacologically active metabolite of MMF, was performed by using an high performance liquid chromatography method.
The water sample was introduced to the PVT cell by using a high-performance piston pump with a set point of <2%% accuracy.
Thermal hazards of benzaldehyde oxime were investigated by using a high-performance adiabatic calorimeter (PHI-TECII) in order to understand its thermophysical properties.
CO-free hydrogen was successfully produced from the dehydrogenation of formic acid at a temperature near its boiling point of 110 °C by using a high-performance non-precious metal molybdenum based catalyst synthesized from soybean and earth-abundant molybdenum.
The produced ethanol was quantified by using a high-performance liquid chromatography (HPLC) system that consisted of a LC-20 AD pump (Shimadzu, Kyoto, Japan), a CTO-20A column oven (Shimadzu), a RID-10A detector (Shimadzu), a YMC-Pack Polyamine II column (4.6 × 250 mm) (YMC Co. Ltd., Kyoto, Japan), and a 7725 injector (Rheodyne, CA, USA).
Methods: rHcy, free Hcy (fHcy), and total Hcy (tHcy), as well as different forms of cysteine, cysteinyl-glycine, and glutathione, were studied by using a high-performance liquid chromatography technique in 19 HD patients, 12 PD patients, 47 patients with CKD, and 15 control subjects.
Therefore, in order to investigate the design of a relief port, research on a 38.6wt% methanol-acetic anhydride system was carried out by using a high-performance adiabatic calorimeter PHI-TEC II, and effects of different volumes of reactors and different masses of reacting substances therein on the area of the relief port were analyzed.
By using a high-performance liquid chromatography (HPLC)/fluorescence assay, they observed that iAsIII and MMAIII increased the BPDE DNA adduct formation in the concentration range being investigated.
Glycated hemoglobin (A1C) was determined by using a high-performance liquid chromatography method with an ADAMS A1C HA-8160 anormalr (normal values 4.0 6.0%; Menarini, Florence, Italy).
AsA content in fruit tissue was determined by using a High-performance liquid chromatography equipment (Jasco) with a reversed-phase column (Gemini® 3 μm C18 Phenomenex, Inc.; Kromasil C18, Scharlau) with ultraviolet detection (254 nm).
