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7 350 auto analyzer

Manufactured by Hitachi
Sourced in Japan

The Hitachi 7,350 auto analyzer is a laboratory instrument designed for automated clinical chemistry analysis. It performs a range of diagnostic tests on biological samples such as blood, urine, and other bodily fluids. The core function of the Hitachi 7,350 is to provide efficient and accurate analysis of various analytes, supporting healthcare professionals in making informed clinical decisions.

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2 protocols using 7 350 auto analyzer

1

Measurement of Cardiometabolic Biomarkers in Fasting Serum

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Venous blood samples were obtained in the morning following an overnight fast. Serum lipids were measured using a Hitachi 7,350 auto analyzer (Hitachi, Tokyo, Japan). Low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglyceride (TG) were determined by the enzymatic method, and LDL-C was determined by the direct method. Fasting plasma glucose levels were measured using a standard enzymatic method. Hemoglobin A1c (HbA1c) (%) was measured by high-performance liquid chromatography using a Tosoh HLC-723 G8 (Tosoh, Kyoto, Japan) and expressed as National Glycohemoglobin Standardization Program (NGSP) values by adding 0.4% to the HbA1c values, which were expressed as conventional Japanese standard substance (JDS) values (15 ). The homeostasis model assessment of insulin resistance (HOMA-IR) was calculated as follows: fasting plasma glucose (FPG) (mg/dL) × fasting plasma insulin (FPI) (μU/mL) / 405. Anti-cyclic citrullinated peptide antibody was measured using a chemiluminescence enzyme immunoassay (CLEIA) (STACIA System; LSI Medience Corporation, Tokyo, Japan). Matrix metalloproteinase-3 was measured using a latex turbidimetric immunoassay (LTIA) (JCA-BM8000 series; JEOL, Tokyo, Japan). Pentraxin-3 was measured using an enzyme-linked immunosorbent assay (ELISA) (human pentraxin-3 ELISA System; Perseus Proteomics, Tokyo, Japan).
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2

Metabolic Biomarkers in Fasting Blood Samples

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Blood samples were collected early in the morning after at least 12-h fasting, through a venous line placed in the median vein using an indwelling catheter. PG level was measured with the glucose oxidase method. HbA1c was measured via high-performance liquid chromatography (HPLC) using a Tosoh HLC-723G8 (Tosoh, Kyoto, Japan). HbA1c (%) was estimated as the National Glycohemoglobin Standardization Program (NGSP) equivalent value, which was calculated as HbA1c (NGSP) (%) = HbA1c (JDS) (%) + 0.4%, considering the relationship of HbA1c (NGSP) values to HbA1c (JDS) (%) values determined by the Japanese standard and measurement method. HOMA-IR, which represents insulin resistance, was calculated using the following formula: HOMA-IR = Fasting glucose level × Fasting insulin level ÷ 405. Measurement of lipid profiles and other markers was outsourced to SRL Co. (Tokyo, Japan). Plasma lipid was measured with a Hitachi 7,350 autoanalyzer (Hitachi, Tokyo, Japan). LDL-C was measured using the colestest LDL (Sekisui Medical, Tokyo, Japan) by the direct method. HDL-C was measured using the colestest NHDL (Sekisui Medical) by the direct method. TG was measured using the pureanto STG-N (Sekisui Medical) by the enzymatic method. HMW-AN was measured via a chemiluminescent enzyme immunoassay. u-C-peptide reactivity (CPR) level was measured in 24-h urine samples.
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