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Ion exchange high performance liquid chromatography method

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The ion-exchange high-performance liquid chromatography (HPLC) method is a laboratory technique used for the separation and purification of charged molecules, such as proteins, peptides, and nucleic acids. This method utilizes a stationary phase containing charged functional groups that interact with the charged analytes, allowing for their separation based on their charge and size characteristics. The core function of this technique is to provide a reliable and efficient means of isolating and analyzing charged biomolecules in a complex mixture.

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2 protocols using ion exchange high performance liquid chromatography method

1

Blood Sampling and Biomarker Analysis

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Upon participant arrival at the laboratory (V1), a 20‐gauge polyethylene catheter was inserted into a forearm vein for blood sampling. Blood samples were drawn at rest after an overnight fasting. Fasting blood glucose was measured using the hexokinase method (Roche Diagnosis, Indianapolis, Indiana). Glycated hemoglobin was assayed using the ion‐exchange high‐performance liquid chromatography method (Bio‐Rad, Hercules, California). Serum cholesterol, triglycerides and high‐density lipoprotein‐cholesterol were analyzed as previously described (Poirier et al. 2000, 2001). Low‐density lipoprotein‐cholesterol was calculated using Friedewald's formula (Friedewald et al. 1972). The cholesterol/high‐density lipoprotein ratio was also calculated.
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2

Glucose, Insulin, and HbA1c Measurement

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Plasma glucose was measured by the glucose oxidase method (Beckman Instruments, Fullerton, CA) and plasma insulin by a chemiluminescent assay using commercial kits (Immulite, Siemens Ltd., Llanberis, Gwynedd, UK). An ion-exchange high-performance liquid chromatography method (Bio-Rad, Hercules, CA) was used to measure HbA1c. The within-run and between-run coefficients of variation for the HbA1c assay were 0.82% and 0.51%, respectively.
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