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Architect i1000 system

Manufactured by Abbott
Sourced in United States

The Architect i1000 system is an automated immunoassay analyzer designed for clinical diagnostic testing. It is capable of performing a variety of immunoassay tests to detect and measure different analytes in biological samples. The system is equipped with features that enable efficient and reliable sample processing and analysis.

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4 protocols using architect i1000 system

1

Serum-based Viral Antibody Detection

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Serum samples were used for antibody detection against several pathogens. Anti-dengue immunoglobulin G (IgG) and IgM were detected using SD BIOLINE Dengue Duo rapid test (Abbott), following manufacturer’s instructions. Anti-Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV), and Hepatitis C Virus (HCV) as well as anti-IgM against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-COV-2) were detected by chemiluminescence immunoassay using the Architect I1000 system (Abbott), following manufacturer’s instructions.
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2

Correcting Systematic Biases in Tacrolimus Assays

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In Changhai Hospital, Chemiluminescence microparticle immunoassay (CMIA) was performed using an Architect I 1000 system (Abbott Laboratories, Abbott Park, IL, USA) to determine tacrolimus blood concentration. The lower limit of quantitation (LOD) was 1.5 ng·mL−1 and the calibration range was between 2.0 and 30 ng·mL−1.28 (link) In Huashan Hospital, enzyme multiplied immunoassay technique (EMIT) was used with a SYVA Viva-Emit 2000 kit (Siemens Healthcare Diagnostics Inc., Germany). The calibration range was 2.0–30 ng·mL−1 and LOD was 2 ng·mL−1.29 There were systematic biases between CMIA and EMIT. Thus, to correct these biases, the data from Huashan Hospital were converted to their corresponding equivalents in terms of the reported bioassays using the following formula:28 (link)
CMIA=0.93*EMIT+0.36.
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3

Vancomycin Dosing and Monitoring

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The vancomycin dosing regimen consisted of 500 mg (every 6 h, 8 h, 12 h, 24 h, 48 h) and 1000 mg (every 8 h, 12 h), for 1.5–2 h intravenous infusion. The TDM usually occurred 0.5–2 h before and after the fourth or fifth dose of vancomycin, which were regarded as steady-state concentrations. All the TDM data were collected. All serum concentrations of vancomycin were determined via the chemiluminescence microparticle immunoassay method with the ARCHITECT i1000 system (Abbott Laboratories, Chicago, IL, USA). The coefficient of variation was less than 10%, and the linear range was between 3 and 100 mg/L.
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4

Everolimus and Tacrolimus Pharmacokinetics

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On day 15 after everolimus administration (namely, day 29 after renal transplantation), whole blood samples were collected by venipuncture just prior to (C0) and at 1, 2, 3, 4, 6, 9, and 12 h (C12) after everolimus and tacrolimus administration at 09:00 AM. In addition, for tacrolimus, whole blood samples were also collected at 24 h after administration. Thereafter, blood concentrations of everolimus and tacrolimus were determined by electrochemiluminescence immunoassay using a Cobas e411 system (Roche, Tokyo, Japan) and chemiluminescence magnetic microparticle immunoassays on an Architect-i1000 system (Abbott Laboratories, Abbott Park, IL, USA), respectively, according to the manufacturers’ instructions.
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