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7600 series automatic biochemical analyzer

Manufactured by Hitachi
Sourced in Japan

The HITACHI 7600 Series Automatic Biochemical Analyzer is a laboratory equipment designed for the automated analysis of biochemical samples. It performs routine clinical chemistry tests, providing accurate and reliable results. The core function of the analyzer is to automate the process of sample processing, reagent handling, and data generation, streamlining the workflow in clinical and diagnostic laboratories.

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6 protocols using 7600 series automatic biochemical analyzer

1

Biochemical Markers in Primary Biliary Cholangitis

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Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), ALP, gamma‐glutaryltransferase (GGT), total bilirubin (TBIL), direct bilirubin (DBIL) and albumin (ALB) in PBC patients was detected by Hitachi 7600 series automatic biochemical analyzer (Japan).
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2

Perioperative Evaluation of Infection

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All blood samples were collected on the day of surgery. The synovial fluid of the knee was collected on the day the blood samples were collected and the synovial fluid of the hip was collected when the capsule was incised intraoperatively. All specimens were submitted for examination within 2 h after collection. To assess CRP levels, plasma and synovial fluid were stored in lithium-heparin vacuum collection tubes. The CRP was tested using a particle-enhanced turbidimetric immunoassay with a HITACHI 7600 Series Automatic Biochemical Analyzer (Hitachi, Tokyo, Japan) and diagnostic kit (DiaSys Diagnostic Systems GmbH, Shanghai, China). Synovial fluid was examined for WBCs and PMNs using a haematology analyzer (Symex XE-5000 haematology analyzer, Symex, Japan), and the synovial fluid was cultured for 14 days on Columbia agar, chocolate agar, and Schaedler agar. At least three suspected tissue specimens were obtained intraoperatively by a stationary surgeon for culture, and the tissue specimens were subjected to intraoperatively frozen section and histopathological examination.
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3

Postoperative Calcium and PTH Monitoring

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Preoperative blood samples were collected on the morning of the operation to determine the preoperative Ca and PTH levels. The postoperative serum Ca and PTH levels were monitored on the morning of the 1st (within 24 hours postsurgery), 3rd, 5th, and 7th postoperative days. A low PTH level was defined as a PTH measurement <15 pg/mL within 24 hours of surgery. Patients were discharged on the 3rd∼7th day postsurgery and were requested to return for clinical follow-up on the 1st, 3rd, 6th, and 12th postoperative months. The serum Ca and PTH levels were measured using a Hitachi 7600 series automatic biochemical analyzer (Hitachi, Tokyo, Japan) and electrochemiluminescence system (Roche Diagnostics GmbH, Mannheim, Germany).
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4

Blood Biomarkers in Clinical Analysis

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The PCT, CRP and WBC levels in the peripheral blood of patients were analyzed at a clinical laboratory in Yijishan Hospital, Wannan Medical College. The PCT was tested using a chemiluminescent immunoassay with an automatic chemiluminescence apparatus (Snibe Diagnostic MAGLUMI 1000) and diagnostic kits (both provided by Shenzhen New Industries Biomedical Engineering Co., Ltd, China). The CRP was tested using a particle-enhanced turbidimetric immunoassay with a HITACHI 7600 Series Automatic Biochemical Analyzer (Hitachi, Ltd., Japan) and diagnostic kits (DiaSys Diagnostic Systems GmbH, Shanghai, China). Routine blood counts were performed with a Mindray BC-6900 hematology analyzer (Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, China). The WBC and neutrophil/lymphocyte ratio (NLR) were calculated based on the routine blood count results. All operations were strictly conducted according to the instructions provided by the instrument and reagent manufacturers.
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5

Quantification of Synovial Fluid IL-6 and Serum CRP

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Synovial fluid (1 ml to 2 ml) and serum samples were obtained soon after admission. The samples were centrifuged at 2,000 rpm for ten minutes within two hours after collection to remove all cellular and particulate content. The levels of IL-6 in the synovial fluid and serum were determined by using the IMMUNOLITE 1000 Immunoassay System (SIEMENS Healthcare, Erlangen, Germany). The CRP was tested using a particle-enhanced turbidimetric immunoassay with a HITACHI 7600 Series Automatic Biochemical Analyzer (Hitachi, Tokyo, Japan) and diagnostic kit (DiaSys Diagnostic Systems GmbH, Shanghai, China).
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6

Rat Model of Chronic Kidney Disease

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This animal study protocol was reviewed and approved by the animal ethics committee of Renji hospital affiliated to Shanghai Jiao Tong University School of Medicine. 24 Sprague-Dawley (SD) rats were randomly divided into two groups: a 5/6 nephrectomy group (n = 12) and a sham-operated group (n = 12). At eight weeks old, rats in the former group received 5/6 nephrectomy, as previously reported [10 (link), 11 (link)]. Supplementary Figure S1-S4 offered a detailed description of the surgical procedure. Baseline, four-week and eight-week postoperative body weights of rats in both groups were recorded. Serum creatinine and blood urea nitrogen (BUN) were assessed four weeks after the surgery utilizing Hitachi 7600 Series Automatic biochemical analyzer (Hitachi, Japan). Rats were identified as successful uremic models if they met both of the following criteria simultaneously: (1) A total mass of the two resected kidneys should reach 0.74% of their body weight. (2) Four weeks after 5/6 nephrectomy, serum creatinine and BUN levels should be 2-3 times higher than those of sham-operated group [10 (link)].
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