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Silica gel tubes

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Silica gel tubes are a type of laboratory equipment used for the collection and storage of samples. They consist of a tube containing silica gel, which is a desiccant material that helps maintain a dry environment within the tube. The primary function of silica gel tubes is to preserve the integrity of the samples during transport and storage.

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4 protocols using silica gel tubes

1

Glucose Tolerance and Metabolic Markers

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The participants were instructed to avoid consuming alcohol and doing strenuous physical activity the day before the visit. After an overnight fast, venous blood samples were drawn. For the oral glucose tolerance test (OGTT), the participants were instructed to drink a 75-g anhydrated glucose drink (Esteriplas, Portugal) in less than 5 min within 10 min after a fasting venous blood sample. Then, the participants were instructed to avoid eating, drinking, and doing any activity and to remain in the waiting room until the postprandial blood samples were drawn 2 h after finishing the glucose drink.
We obtained serum from silica gel tubes (Becton, Dickinson and Company) kept at room temperature for 30–60 min before centrifugation (1500 g, 15 min). Plasma was obtained from EDTA tubes (Becton, Dickinson and Company) that were immediately placed on ice and centrifuged within 10 min (2000 g, 4 °C, 15 min). Serum concentrations of standard biochemical parameters, including fasting and 2-h OGTT glucose, insulin, HbA1c, triglycerides, total-, LDL-, and HDL-cholesterol and high-sensitive C-reactive protein were measured by standard methods at an accredited routine laboratory (Fürst Medical Laboratory, Norway).
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2

Fasting Blood Sampling and Metabolic Evaluation

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Venous blood samples were drawn after an overnight fast (≥10 h). Serum was obtained from silica gel tubes (Becton, Dickinson, and Company, San Jose, CA, USA) and kept at room temperature for 30–60 min until centrifugation (1500× g, 15 min). Plasma was obtained from K2EDTA tubes (Becton, Dickinson, and Company), immediately placed on ice, and centrifuged within 10 min (2000× g, 4 °C, 15 min).
Serum concentrations of fasting glucose, insulin, HbA1c, triglycerides, total cholesterol, LDL-cholesterol, HDL-cholesterol, high-sensitive C-reactive protein (hsCRP), and glucose and insulin after a 2 h OGTT (75 g glucose load) were measured by standard methods at an accredited routine laboratory (Fürst Medical Laboratory, Oslo, Norway).
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3

Fasting Blood Sample Collection

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Participants were instructed to avoid consumption of alcohol and doing vigorous physical activity the day before blood sampling. Venous blood samples were drawn after an overnight fast (≥10 h). Serum was obtained from silica gel tubes (Becton, Dickinson and Company, Franklin Lakes, NJ, USA) and kept at room temperature for >30-60< min, until centrifugation (1500 × g, 15 min). Plasma was obtained from K2EDTA tubes (Becton, Dickinson and Company, Franklin Lakes, NJ, USA), immediately placed on ice, and centrifuged within 10 min (2000 × g, 4°C, 15 min). Lithium-Heparin tubes (Becton, Dickinson and Company, Franklin Lakes, NJ, USA) and K2EDTA tubes with whole blood were kept at room temperature. Serum and plasma concentrations of fasting glucose, insulin, HbA1c, TG, total-cholesterol, LDL-C, HDL-C, hsCRP, creatinine, eGFR, ASAT, ALAT, Gamma-GT and mercury, and glucose and insulin after a 2h-OGTT, were measured by standard methods at an accredited routine laboratory (Fürst Medical Laboratory, Oslo, Norway).
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4

Lipid and CRP Measurements in Fasting Samples

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Fasting blood samples were drawn at baseline and after three weeks. Serum was obtained from silica gel tubes (Becton Dickinson) kept in room temperature for at least 30 minutes, until centrifugation at 1500g for 12 minutes. Plasma was obtained from EDTA tubes (Becton Dickinson), immediately placed on ice and centrifuged within 10 minutes (1500 rpm, 4°C, 15 minutes). The plasma samples were frozen and stored at -80°C until further analysis.
Routine measurements were analyzed at the central laboratory of Oslo University Hospital, Rikshospitalet. Plasma (P)-TC and P-triglyceride (TG) was measured with an enzymatic colorimetric assay, while P-LDL-C and P-high density lipoprotein cholesterol (HDL-C) was measured with a homogeneous enzymatic colorimetric assay. P-C.reactive protein (CRP) was measured by particle reinforced immunoturbidimetric assay and serum-glucose was measured enzymatic with hexokinase. All analyses were carried out on Cobes 8000, c702. ApoA1 and ApoB were measured by turbidometry on Cobas c501. The instruments, reagents and calibrator were delivered from Roche Diagnostics (Mannheim, Germany). All analyzes were accredited after International and European standard NS-EN ISO 15189
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