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Aia 2000 la

Manufactured by Tosoh
Sourced in Japan

The AIA-2000 LA is an automated immunoassay analyzer developed by Tosoh. It is designed for the quantitative determination of various analytes in biological samples using immunoassay techniques.

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6 protocols using aia 2000 la

1

Glycemic Markers and Lipid Profiles

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The OGTTs were performed after 10‐hour fasts with 0‐, 30‐, 60‐ and 120‐minute samplings to establish plasma glucose and insulin levels, and at the preload time, serum high‐density lipoprotein cholesterol (HDL‐C), low‐density lipoprotein cholesterol (LDL‐C), triglyceride (TG), haemoglobin A1c (HbA1c) and glycoalbumin (GA) were measured. Excluded from this study were subjects who were over 30 years of age.
We classified 575 subjects into the NGT group, 19 into the IGT group, and 1 into the IFG group. We removed the subjects with IGT and IFG from further analyses in this analysis. We found no subjects with apparent T2DM.
We measured height and weight and calculated BMIs (weight [kg]/height [m2]). We used enzymatic methods to measure serum HDL‐C, LDL‐C, TG and GA concentrations, with an automatic analyser (LABOSPECT 008; Hitachi). Serum insulin concentrations were measured by chemiluminescence immunoassay using an automatic analyser (AIA‐2000 LA; Tosoh). Plasma glucose concentrations were measured using a hexokinase method, and HbA1c levels were measured by high‐performance liquid chromatography, using automatic analysers (ADAMS Glucose GA‐1170 and ADAMS A1c HA8180, respectively; Arkray).
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2

Comprehensive Hematological and Metabolic Assessment

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Hematocrit, white blood cell (WBC) count, and platelet count were measured using an automated hematology analyzer (Sysmex XE-5000; Sysmex Corporation, Kobe, Japan). Fibrinogen concentration was measured by the Clauss method using an automated coagulation analyzer (Sysmex CS-5100; Sysmex Corporation). Serum TC, TG, HDL-C, and LDL-C levels were measured by enzymatic methods, and C-reactive protein (CRP) levels were measured by latex immunoassay, using an automatic analyzer (LABOSPECT008; Hitachi High-Technologies Corporation, Tokyo, Japan). Serum insulin levels were measured by chemiluminescence immunoassay using an automatic analyzer (AIA-2000 LA; Tosoh Corporation, Tokyo, Japan). Plasma glucose levels were measured by the hexokinase method, and hemoglobin A1c levels were measured by high-performance liquid chromatography, using automatic analyzers (ADAMS Glucose GA-1170 and ADAMS A1c HA-8180; ARKRAY, Inc., Kyoto, Japan). Whole blood viscosity levels were measured at 60 revolutions/min using a micro cone-plate viscometer (LVDV-II + Pro CP; Brookfield Engineering Laboratories, Middleboro, MA, USA) [36 (link)]. The inter- and intra-assay coefficients of variation for BPT were 7% and 5% , respectively.
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3

Anthropometric and Metabolic Assessments

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We measured participants’ heights and weights and calculated body mass index (BMI; weight (kg)/height (m2)). Fasting serum HDL-C, LDL-C, and TG concentrations were measured by enzymatic methods with an automatic analyzer (LABOSPECT 008; Hitachi, Tokyo). Serum insulin concentrations were also measured by chemiluminescence immunoassay using an automatic analyzer (AIA-2000 LA; Tosoh, Tokyo). We further measured plasma glucose concentrations by a hexokinase method and HbA1c levels using high-performance liquid chromatography, with automatic analyzers (ADAMS Glucose GA-1170 and ADAMS A1c HA8180, respectively; Arkray, Tokyo, Japan).
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4

Lipid Profile and Metabolic Biomarkers Evaluation

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Circulating levels of HDL-C, LDL-C, TG, and FFA were measured using enzymatic methods (LABOSPECT 008, Hitachi, Tokyo, Japan). Serum LPL concentrations were determined using an LPL assay kit (SEKISUI MEDICAL Co. Ltd., Tokyo, Japan) based on a sandwich enzyme-linked immunosorbent assay (ELISA) [19 (link)]. A human GPIHBP1 assay kit and a human serum HTGL ELISA kit (Immuno-Biological Laboratories Co., Ltd., Gunma, Japan) were used to estimate serum GPIHBP1 and HTGL concentrations, respectively [19 (link)]. Plasma glucose concentrations were determined using a hexokinase method (ADAMS Glucose GA-1170; Arkray, Kyoto, Japan), and HbA1c levels were measured using high-performance liquid chromatography (ADAMS A1c HA8180; Arkray, Kyoto, Japan). Serum insulin concentrations were measured using chemiluminescence immunoassay (AIA-2000 LA; Tosoh, Tokyo, Japan) [8 (link),19 (link)].
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5

Serum Lipid and Glucose Biomarkers

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Serum HDL-C, LDL-C, TG, and GA concentrations were measured using enzymatic methods (LABOSPECT 008; Hitachi, Tokyo), and serum insulin concentrations were measured using chemiluminescence immunoassay (AIA-2000 LA; Tosoh, Tokyo). Plasma glucose concentrations were measured using a hexokinase method (ADAMS Glucose GA-1170; Arkray, Tokyo), and HbA1c levels were measured using high-performance liquid chromatography (ADAMS A1c HA8180; Arkray, Tokyo).
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6

Serum Lipid and Enzyme Profiling

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Serum HDL-C, LDL-C, triglycerides, and FFA concentrations were measured by using enzymatic methods (LABOSPECT 008; Hitachi, Tokyo), and serum insulin concentrations were measured by chemiluminescence immunoassay (AIA-2000 LA; Tosoh, Tokyo). Plasma glucose concentrations were measured by using a hexokinase method (ADAMS Glucose GA-1170; Arkray, Tokyo), and HbA1c levels were measured by high-performance liquid chromatography (ADAMS A1c HA8180; Arkray). Serum LPL concentrations were measured by using an LPL assay kit (SEKISUI MEDICAL CO. LTD, Tokyo) based on a sandwich enzyme-linked immunosorbent assay (ELISA) [18] . A Human GPIHBP1 Assay Kit and a Human Serum HTGL ELISA Kit (Immno-Biological Laboratories Co., Ltd., Gunma) based on ELISA were used to determine serum GPIHBP1 and HTGL concentrations, respectively [18] .
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