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Paramagnetic particle chemiluminescent immunoassay

Manufactured by Beckman Coulter

The Paramagnetic Particle Chemiluminescent Immunoassay is a laboratory equipment used for immunoassay analysis. It utilizes paramagnetic particles and chemiluminescent detection technology to measure the presence and concentration of target analytes in a sample.

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3 protocols using paramagnetic particle chemiluminescent immunoassay

1

Hormone and Metabolic Profile Assessment

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Testosterone was measured with a chemiluminescent immunoassay for quantitative determination of total testosterone level in human serum and plasma using the Access Immunoassay System (Beckman Coulter). The detection rate range was between 0.35–55.5 nmol/L). The intra- and inter-assay CV for testosterone were less than 5 percent in both cases. Sexual hormone binding globulin (SHBG) and prolactin were measured with a paramagnetic particle chemiluminescent immunoassay (Beckman Coulter, Inc). The intra-and inter-assay variation for SHBG was 4.0 and 5.5 percent respectively, and for prolactin 3.5 and 5.0 percent. Total cholesterol, High-density lipoprotein (HDL)-cholesterol and HbA1c were measured by the routine chemistry accredited laboratory at the Karolinska University Hospital. LDL-cholesterol was calculated according to the Friedewald formula [10 (link)]. All samples were analyzed according to the manufacturer’s advice at the Department of clinical chemistry, Karolinska University Hospital.
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2

Biomarker Measurement and Validation

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Participants of the EMSI subcohort were instructed to fast for their morning in-home visit. Blood samples were collected in sodium heparin tubes which were processed immediately. Blood samples were assayed for DHEAS, TT and SHBG concentrations by paramagnetic particle chemiluminescent immunoassay (Beckman Coulter, Fullerton, CA) at Harvard Catalyst Clinical Research Center (Boston, MA). All intra-assay coefficients of variation were less than 10% (DHEAS: 1.6–8.3%, TT: 1.7–3.9% and SHBG: 4.5–4.8%) and all Inter-assay coefficients of variation were less than 11% (DHEAS: 3.7–11.3%, TT: 4.2–7.1%, SHBG: 5.2–5.5%).
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3

Metabolic and Inflammatory Biomarker Assessment

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We measured biomarkers of metabolic functioning [hemoglobin A1C (HbA1C) and adiponectnin], and inflammation [high-sensitivity C-reactive protein (hs-CRP), interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-a)]. HbA1C was measured by turbidimetric inhibition immunoassay (Roche Diagnostics, Indianapolis, IN). Adiponectin was measured by enzyme-linked immunosorbent assay (ELISA) (ALPCO Diagnostics Inc, Salem, NH). hs-CRP was measured using particle enhanced turbidimetric assay (Roche Diagnostics, Indianapolis, IN). IL-6 was measured by paramagnetic particle, chemiluminescent immunoassay (Beckman Coulter, Fullerton, CA). TNF-a was measured using quantitative sandwich enzyme immunoassay (R&D Systems Inc., Minneapolis, MN).
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