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7450 analyzer

Manufactured by Hitachi
Sourced in Japan

The 7450 analyzer is a versatile laboratory instrument designed for a range of analytical applications. It offers reliable and accurate measurements, providing users with essential data for their research and testing needs. The core function of the 7450 analyzer is to perform precise analysis and quantification of various samples, making it a valuable tool for laboratories across different industries.

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8 protocols using 7450 analyzer

1

Oral Glucose Tolerance and Metabolic Profiles

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75-g oral glucose tolerance test and blood biochemical measurements were conducted for each subject. All blood samples were obtained after 12-hour fasting. Blood and urine samples were refrigerated at −20°C, transferred and tested in the central laboratory of the First Affiliated Hospital, Xiamen University. Plasma glucose, liver enzyme levels, and serum lipid profiles, including triglyceride (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C) were determined on a HITACHI 7450 analyzer (HITACHI, Tokyo, Japan). Low-density lipoprotein cholesterol (LDL-C) was calculated by Friedewald’s formula. Fasting plasma glucose concentration (FPG) and 2-hour plasma glucose concentration (2hPG) were measured by the hexokinase method. Serum fasting insulin concentration was measured by electrochemiluminiscence immunoassay (Roche Elecsys Insulin Test, Roche Diagnostics, Mannheim, Germany). HOMA-insulin resistance (HOMA-IR) was calculated by fasting serum insulin (Flns, mU/ml) *fasting blood glucose (FPG, mmol/L)/22.5. Raised fasting plasma glucose (FPG) was defined as FPG ≥ 100 mg/dL (5.6 mmol/L) or previously diagnosed type 2 diabetes. Serum uric acid was measured by the auto-analyzer (COBAS INTEGRA 400 plus, Roche, Basel, Switzerland); and hyperuricemia was defined as the serum uric acid level >7.0 mg/dL in males and >6.0 mg/dL in females.
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2

Anthropometric and Metabolic Measurements

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Anthropometric measurements were conducted as described in detail previously [19 (link)]. Subjects underwent weight, height, and WC measurements by using a calibrated scale after removing shoes and heavy clothes. BMI was calculated as the weight in kilograms divided by the square of the height in meters. And overweight and obesity were defined as BMI of 24–27.9 kg/m2 and ≥ 28 kg/m2, respectively [20 ]. WHtR was calculated as the WC in meters divided by the height in meters. Arterial blood pressure was measured with OMRON electronic sphygmomanometer after sitting for at least 15 min. Blood samples were obtained after 12-h fasting for each subject. Lipid profiles (TG, total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-c)) were determined on a HITACHI 7450 analyzer (HITACHI, Tokyo, Japan). Low-density lipoprotein cholesterol (LDL-C) was calculated by Friedewald’s formula. Fasting plasma glucose (FPG) were measured by the hexokinase method. Serum fasting insulin concentration was measured by electrochemiluminescence immunoassay (Roche Elecsys Insulin Test, Roche Diagnostics, Mannheim, Germany). HOMA-IR was calculated using the formula: fasting serum insulin (mU/L) *fasting plasma glucose (mmol/L) /22.5 [21 (link)]. FT3, FT4 and TSH levels were measured using electrochemiluminescence immunoassay.
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3

Evaluation of Metabolic Parameters and NAFLD

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Details on methods of subject sampling and evaluation, including face-to-face interviews and clinical characteristics measurements, have been described previously.18 19 (link) Blood samples were obtained after 12-hour fasting and tested in the central laboratory of the First Affiliated Hospital, Xiamen University. Plasma glucose, liver enzymes and serum lipid profiles, including triglyceride (TG), total cholesterol (TC) and high-density lipoprotein-cholesterol (HDL-C) were determined on a HITACHI 7450 analyzer (HITACHI, Tokyo, Japan). Homeostasis model assessment-insulin resistance (HOMA-IR) was calculated using the formula: fasting serum insulin (mU/L)×fasting plasma glucose (FPG) (mmol/L)/22.5. And IR was defined as HOMA-IR ≥2.6×10−6 mol×IU/L2.20 (link) Hepatic ultrasonography scanning and diagnosis of hepatic steatosis have been described previously18 19 (link) and followed the guidelines for the diagnosis and treatment of NAFLDs in China (Chinese National Consensus Workshop on NAFLD).21 (link)
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4

Plasma Lipid and Glucose Profiling

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Blood samples were obtained after 12-hour fasting and tested in the central laboratory of the First Affiliated Hospital, Xiamen University, Xiamen, China. Plasma glucose and serum lipid profiles, including triglyceride (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C) were determined on a HITACHI 7450 analyzer (HITACHI, Tokyo, Japan). Low-density lipoprotein cholesterol (LDL-C) was calculated by Friedewald's formula. Fasting plasma glucose (FPG) concentration was measured by the hexokinase method. Serum fasting insulin concentration was measured by an electrochemiluminiscence immunoassay (Roche Elecsys Insulin Test, Roche Diagnostics, Mannheim, Germany). Homeostasis model assessment of insulin resistance (HOMA-IR) was calculated using the formula: fasting serum insulin (mU/L) FPG (mmol/L) /22.5. And insulin resistance was defined as HOMA-IR ≥2.6×10−6 mol Meex IU/L−2.[15 (link)]
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5

Oral Glucose Tolerance and Metabolic Profiles

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75-g oral glucose tolerance test and blood biochemical measurements were conducted for each subject. All blood samples were obtained after 12-hour fasting. Blood and urine samples were refrigerated at −20°C, transferred and tested in the centre laboratory of the First Affiliated Hospital, Xiamen University. Plasma glucose, liver enzyme levels, and serum lipid profiles, including triglyceride (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C) were determined on a HITACHI 7450 analyzer (HITACHI, Tokyo, Japan). Low-density lipoprotein cholesterol (LDL-C) was calculated by Friedewald's formula. Fasting plasma glucose concentration (FPG) and 2-hour plasma glucose concentration (2hPG) were measured by the hexokinase method. Serum fasting insulin concentration was measured by electrochemiluminiscence immunoassay (Roche Elecsys Insulin Test, Roche Diagnostics, Mannheim, Germany). HOMA-insulin resistance (HOMA-IR) was calculated by fasting serum insulin (Flns, mU/ml) *fasting blood glucose (FPG, mmol/L)/22.5. HOMA-β was calculated by 20*fasting serum insulin (Flns, mU/ml)/(fasting blood glucose (FPG, mmol/L)-3.5).
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6

Anthropometric and Metabolic Measurements

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Anthropometric measurements including body weight, height, WC, blood pressure (BP), and BMI were described previously [15 (link), 16 ]. BMI was calculated as the weight in kilograms divided by the square of the height in meters. After 12-hour fasting, all blood samples were obtained. Blood samples were measured in the central laboratory of the First Affiliated Hospital, Xiamen University. Briefly, hemoglobin A1c (HbA1c) was measured by the Bio-Rad Variant Hemoglobin A1c assay. TG, total cholesterol (TC), high-density lipoprotein cholesterol (HDL-c), and low-density lipoprotein cholesterol (LDL-c) were determined on a HITACHI 7450 analyzer (HITACHI, Tokyo, Japan).
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7

Plasma Biochemical Profiling Protocol

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The plasma total cholesterol, triglyceride, HDL cholesterol, aspartate aminotransferase (AST), alanine aminotransferase (ALT), total protein (TP), albumin (ALB), urea nitrogen (UN) and uric acid (UA) were measured on a Hitachi 7450 Analyzer (Hitachi, Japan) using Roche reagents.
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8

Anthropometric and Metabolic Measurements

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A spring scale and a vertical ruler measure were used to obtain bodyweight and height measurements, respectively. Body mass index (BMI) measures total body adiposity. Waist circumference was measured at the level of the umbilicus. Blood pressure (BP) was assessed in triplicate using an electronic sphygmomanometer (OMRON Company). Body fat mass was determined using the HOLOGIC whole body DXA system (Hologic Inc., Bedford, MA). Each measurement was performed at least three times, and the mean value was used for analysis.
Each subject underwent 75-g oral glucose tolerance tests and blood biochemical measurements a 12 h fast. Plasma glucose, high-density lipoprotein cholesterol (HDL-c), triglycerides (TG), and total cholesterol (TC) were measured by enzymatic colorimetric methods with a Hitachi 7450 analyzer (Hitachi, Tokyo, Japan). Low-density lipoprotein cholesterol (LDL-C) was calculated by Friedewald’s formula. Fasting plasma glucose concentrations and 2-h glucose concentrations were measured using the glucose oxidase method. Serum insulin concentrations were measured using electrochemiluminescence immunoassay (Roche Elecsys Insulin Test, Roche Diagnostics, Mannheim, Germany). Insulin resistance was estimated using HOMA of insulin resistance (HOMA-IR).
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