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30 protocols using architect i2000sr immunoassay analyzer

1

Comprehensive Blood Profile Analysis

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Peripheral venous blood samples were sampled via the antecubital vein in the morning after an overnight fasting. Complete blood counts and differential counts were analyzed by the automated cellular analysis system Beckman Coulter DxH 800 hematology analyzer (Beckman Coulter, Miami, FL). Biochemical parameters of albumin, lipid profile, high sensitive-C reactive protein (hs-CRP), fasting glucose, aspartate transaminase, blood urea nitrogen, and serum creatinine were measured by the ARCHITECT i2000SR immunoassay analyzer (Abbott Diagnostics, Abbott Park, IL, USA). Lymphopenia was defined by absolute lymphocyte count < 1000/cumm [29 (link)].
Lymphocyte subsets were determined flow-cytometric analysis system Beckman Coulter FC500 flow cytometer (Beckman Coulter, Miami, FL) in freshly drawn peripheral blood after adequate processing as the manufacturer’s instruction. Serum CMV IgG, VZV IgG, HBsAg IgG, HCV IgG, and C. pneumoniae IgG were measured by a chemiluminescent immunoassay on the ARCHITECT i2000SR immunoassay analyzer (Abbott Diagnostics, Abbott Park, IL, USA).
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2

Multimodal Hepatitis B Biomarker Profiling

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Hepatitis B virus surface antigen, HBsAb, HBeAg, HBeAb, and HBcAb were measured by chemiluminescence using the Architect i2000SR Immunoassay Analyzer (Abbott Diagnostics, Abbott Park, Illinois, USA). Results of HBsAg were presented in IU/ml and HBsAb in mIU/ml, both with corresponding ranges. The results of HBeAg, HBeAb, and HBcAb were all presented in relative luminescence unit signal over cutoff ratio (s/co). Cutoff value and ranges were as follows: 0.05 and 0.0–250 IU/ml for HBsAg; 10 and 0.00–1,000.00 mIU/ml for HBsAb; 1.00 s/co as the cutoff for HBeAg and HBcAb, a value higher than 1.00 was considered as positive; 1.00 s/co set as the cutoff for HBeAb, a value higher than 1.00 were defined as negative. If a result fell in the gray zone, the sample was subjected to duplicate retesting and considered repeatedly reactive when both turned reactive. If both the retests were negative, we considered the original sample negative. When contradictory results appeared, we initiated external validation by Cobas e 801 analytical unit for immunoassay tests (Roche Diagnostics, Indianapolis, USA). HLA-B27 positivity was determined in the blood samples by the flow cytometric approach.
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3

Troponin I Level Measurement Techniques

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For the measurement of troponin I levels, ARCHITECT i2000SR immunoassay analyzer (Abbott Diagnostics, TX, USA; measurement range, 0.00-50.0 ng/mL; Hallym University Sacred Heart Hospital), ADVIA Centaur XP immunoassay system (Siemens Medical Solutions Diagnostics, Tarrytown, NY, USA; measurement range, 0.006-50.0 ng/mL; Chuncheon Sacred Heart Hospital), and UniCel DxI 800 immunoassay analyzer (Beckman Coulter, Villepinte, France; measurement range, 0.03-80.0 ng/mL; Kangdong Sacred Heart Hospital) were used. In this study, all troponin I levels were also obtained within 1 hr after presentation to the emergency room or after admission.
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4

Plasma Galectin-3 Measurement Protocol

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Galectin-3 concentrations were measured in blood specimens collected from participants at visit 4 (1996-1998), processed, and stored as plasma in tubes containing EDTA as an anticoagulant at -70°C until laboratory analysis. Plasma galectin-3 concentrations were measured using a chemiluminescent micro-particle immunoassay on the ARCHITECT i2000SR Immunoassay Analyzer (Abbott Diagnostics, Abbott Park, Illinois).33 (link)
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5

Serum HE4 Measurement Protocol

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Demographic and clinical characteristics and laboratory findings were collected on the day of renal biopsy and comprised information about age, gender, body mass index, and hematological, biochemical, and immunological test results. Serum HE4 level was measured using Architect HE4 kits and an Abbott ARCHITECT i2000SR Immunoassay Analyzer (Abbott Laboratories, Abbott Park, IL, USA) according to the manufacturer’s instructions. Briefly, a two-step immunoassay involving the chemiluminescent microparticle immunoassay technology with flexible assay protocols (Chemiflex) was used.
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6

Serum Biomarker Measurement Protocol

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With the participant in the sitting position, blood samples were collected from the antecubital vein using 23-G needles [11 ]. The serum samples were separated by centrifugation (1500×g) at 4 °C for 10 min and were stored at − 80 °C until analysis [11 ]. A LABOSPECT 008 automatic analyzer (Hitachi, Tokyo, Japan) was used to measure serum albumin concentrations using the modified bromocresol purple method, and serum transthyretin and transferrin concentrations using turbidimetric immunoassays. Intra- and inter-assay CV were 0.5–0.7 and 1.5% for albumin, 1.3–1.8% and 0.6–1.1% for transthyretin, and 0.8–1.2% and 1.3–1.4% for transferrin, respectively. A chemiluminescent microparticle immunoassay on an Abbott ARCHITECT i2000SR Immunoassay Analyzer (Abbott Laboratories, Abbott Park, IL, USA) was used to analyze serum concentrations of free 3,5,3′-triiodothyronine (FT3), free thyroxine (FT4), and thyrotropin (TSH). Intra- and inter-assay CV were 5.1–5.7% and 0.5–2.8% for FT3, 3.6–4.5 and 4.1% for FT4, and 2.3–4.4% and 2.8–4.1% for TSH, respectively. Serum BTR was measured by the enzymatic method using JCA-BM6050 automatic analyzer (JOEL, Tokyo, Japan) at LSI Medience Co. (Tokyo, Japan). Intra- and inter-assay CV of BTR were 0.2–0.3% and 0.7–1.0%, respectively.
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7

Blood Biomarker Quantification Protocol

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With the participant sitting, blood samples were collected from an antecubital vein using 23-G needles. The serum samples were separated by centrifugation (1,500 × g) at 4 °C for 10 min and were stored at -80 °C until analysis. A LABOSPECT 008 automatic analyzer (Hitachi, Tokyo, Japan) was used to measure serum albumin concentrations using the modified bromocresol purple method, serum retinol binding protein (RBP) concentrations using latex turbidimetric immunoassays, and serum transthyretin and transferrin concentrations using turbidimetric immunoassays. A chemiluminescent microparticle immunoassay on an Abbott ARCHITECT i2000SR Immunoassay Analyzer (Abbott Laboratories, Abbott Park, IL, USA) was used to analyze serum concentrations of free 3,5,3′-triiodothyronine (FT 3 ), free thyroxine (FT 4 ), and thyrotropin (TSH). Serum BTR was measured by the enzymatic method by LSI Medience Co. (Tokyo, Japan).
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8

Quantitative Biomarker Measurement in Serum

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With the participant sitting, blood samples were collected from an antecubital vein using 23-G needles. The serum samples were separated by centrifugation (1,500 × g) at 4 °C for 10 min and were stored at -80 °C until analysis. A LABOSPECT 008 automatic analyzer (Hitachi, Tokyo, Japan) was used to measure serum albumin concentrations using the modi ed bromocresol purple method, serum retinol binding protein (RBP) concentrations using latex turbidimetric immunoassays, and serum transthyretin and transferrin concentrations using turbidimetric immunoassays. A chemiluminescent microparticle immunoassay on an Abbott ARCHITECT i2000SR Immunoassay Analyzer (Abbott Laboratories, Abbott Park, IL, USA) was used to analyze serum concentrations of free 3,5,3′-triiodothyronine (FT 3 ), free thyroxine (FT 4 ), and thyrotropin (TSH). Serum BTR was measured by the enzymatic method by LSI Medience Co. (Tokyo, Japan).
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9

Liver Function Biomarkers Measurement

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Serum alanine transaminase (ALT), aspartate aminotransferase (AST), total bilirubin (TBil) and albumin (ALB) levels were measured by routine laboratory tests at the Department of Laboratory Science of Anhui Provincial Hospital (Hefei, China). In addition, serology tests were performed on the ARCHITECT i2000SR immunoassay analyzer (Abbott Pharmaceutical Co., Ltd.) and serum HBV DNA levels were measured using the COBAS TaqMan HBV test (Roche Diagnostics).
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10

Serum Lipid and Enzyme Analysis

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With the participants sitting down, blood samples were collected after an antecubital vein is punctured using 23-G needles. Serum samples were separated by centrifugation (1500×g) at 4 °C for 10 min and were stored at − 80 °C until analysis. A chemiluminescent microparticle immunoassay on an Abbott ARCHITECT i2000SR Immunoassay Analyzer (Abbott Laboratories, Abbott Park, Illinois) was used to analyze the serum concentrations of free 3,5,3′-triiodothyronine (FT3), free thyroxine (FT4), and thyrotropin (TSH). Enzymatic methods using a LABOSPECT 008 automatic analyzer (Hitachi, Tokyo, Japan) were carried out to measure serum total cholesterol (TC), HDL cholesterol (HDL-C), and TG concentrations. The Friedewald formula was used to determine LDL cholesterol (LDL-C) concentrations: LDL-C = TC − HDL-C − TG/5 [40 (link)].
LPL latex agglutination turbidimetry (Immuno-Biological Laboratories [IBL], Gunma, Japan) was used to measure serum LPL concentrations [35 (link)]. A Human GPIHBP1 Assay Kit (IBL) based on sandwich ELISA was used to determine serum GPIHBP1 concentrations [36 (link)]. Finally, the Human Serum HTGL ELISA Kit (IBL) was used to measure serum HTGL concentrations [34 (link)].
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