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Vitros 5.1 fs system

Manufactured by Ortho Clinical Diagnostics

The Vitros 5.1/FS system is an automated clinical chemistry analyzer designed for in vitro diagnostic testing. It is capable of performing a variety of assays to measure different analytes in biological samples.

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2 protocols using vitros 5.1 fs system

1

Intravenous Glucose Tolerance Test for Diabetes

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An intravenous glucose tolerance test (IVGTT) was performed under full GA prior to the animal being rendered diabetic, after induction of diabetes, and post-transplant at monthly intervals. An intravenous bolus of dextrose (0.5 g/kg body weight) was injected into the cephalic venous line followed by a saline flush. Blood samples were obtained before injection and at 1, 2.5, 3, 5, 7.5, 10, 15, 20, 30, 40, 45, 50, 60, 75, 90, 105 and 120 min after injection. Blood glucose concentrations were measured using a dry chemistry method on a Vitros 5.1/FS system (Ortho-Clinical Diagnostics, Rochester, NY). NHP and porcine insulin were measured using Mercodia Insulin ELISA and c-peptide concentrations were measured using a Mercodia Porcine C-peptide ELISA (Mercodia AB, Uppsala, Sweden). K values [percentage decline of natural logarithm (blood glucose)/min] were calculated with blood glucose measurements from the IVGTT.
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2

Comprehensive Metabolic Profiling Protocol

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Serum and plasma were prepared from collected venous blood samples (15 mL) and then
frozen (-80°C) for storage until analysis.
Insulin levels were determined by chemiluminescence and processed in the IMMULITE
2000 (Siemens Healthcare Diagnostics Products Ltd) analyzer, and glucose levels were
analyzed in the VITROS 5.1 FS system (Ortho Clinical Diagnostics, Johnson &
Johnson) with Micro SlideTM technology. HOMA-IR was calculated based on
the formula: HOMA-IR = insulin (mU/L) x glucose (mmol/L)/22.5, taking 3 as the cutoff
value for the diagnosis of insulin resistance.
Total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein
cholesterol and triglyceride levels were measured using an automated biochemical
VITROS 5.1 FS analyzer (Ortho Clinical Diagnostics, Johnson & Johnson).
Apolipoprotein A-I, B and lipoprotein (a) levels were determined by
immunonephelometry and processed in the BN ProSpec® System (Siemens Healthcare
Diagnostics Inc.) analyzer.
Leptin (eBioscience, San Diego, CA, USA) and adiponectin (BioVendor, Brno, Czech
Republic) were evaluated using commercially available enzyme-linked immunosorbent
assay kits, and the absorbances were measured at 450 nm (BIO-RAD Microplate Reader
Model 680, Hercules, CA, USA).
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