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One touch 2 blood glucose monitoring system

Manufactured by LifeScan
Sourced in United States

The OneTouch II blood glucose monitoring system is a device designed to measure and display the level of glucose in a person's blood. It is a compact, handheld device that uses a small sample of blood to provide the user with a reading of their current blood glucose level.

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9 protocols using one touch 2 blood glucose monitoring system

1

Comprehensive Arterial Blood Analysis

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Some arterial blood (180 μL) was used to analyse the levels of pH, carbon dioxide tension (PaCO2), bicarbonate (HCO3-), base excess and potassium concentration by an arterial blood gas analyzer (AVL OPTI Critical Care Analyzer, AVL Scientific Corp., Roswell, GA, USA). Blood glucose was analysed by a One-Touch II blood glucose monitoring system (Lifescan Inc., Milpitas, CA, USA) with 10 μL of whole blood. The remaining blood was then immediately centrifuged at 7,500 g for 2 minutes to obtain the plasma. Plasma (80 μL) was used to analyse the biochemical parameters of liver and kidney function. Liver function was assessed by measuring plasma levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT), and renal function was assessed by plasma levels of blood urea nitrogen (BUN) and creatinine. In addition, plasma lactate dehydrogenase (LDH) was measured to evaluate the extent of organ injury. All of these biochemical parameters were analysed by Fuji DRI-CHEM 3030 (Fuji Photo Film Co., Ltd., Tokyo, Japan).
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2

Blood Pressure and Glucose Monitoring

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We used an MK-2000A blood pressure monitor (Muromachi Kikai, Tokyo, Japan) to detect baseline SBP and HR and those 24 h after saline or LPS administration. In addition, 10 μl of whole blood was taken to evaluate the glucose levels using a One Touch II blood glucose monitoring system (Lifescan, Milpitas, CA, USA).
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3

Measuring Blood Glucose and Gas Levels

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Before the blood sample was centrifuged to prepare serum, ten microliters of whole blood was taken to measure the glucose level in blood by a One Touch II blood glucose monitoring system (Lifescan, Milpitas, CA, USA). One hundred and eighty microliters of whole blood was used to examine the levels of HCO3-, BE, PaCO2, and PaO2 by an arterial blood gas analyzer (AVL OPTI Critical Care Analyzer, AVL Scientific Corp., Roswell, GA, USA).
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4

Blood Glucose Monitoring after LPS

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Blood samples were drawn at baseline (i.e., time 0) and at 1, 2, 4, 6 h after vehicle or LPS. Ten microliters of whole blood was immediately used to analyze the glucose levels by a One Touch II blood glucose monitoring system (Lifescan, Milpitas, CA, USA).
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5

Comprehensive Metabolic Assessment

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Blood glucose was determined by a One-Touch II blood glucose monitoring system (Lifescan, Milpitas, CA, USA) with 10 μL of whole blood. Fuji DRI-CHEM 3030 Analyzer (Fuji Photo Film Co., Ltd., Tokyo, Japan) was used to evaluate the indexes of organ function. Liver function and renal function were determined by measuring plasma concentrations of alanine aminotransferase (ALT) and creatinine, respectively. In addition, lactate dehydrogenase (LDH) was surveyed to assess the severity of tissue injury.
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6

Glucose Levels During LPS Challenge

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At baseline (i.e., time 0) and at 1, 2, 4, 6 h after saline or LPS, blood samples were taken to measure the glucose levels by a One Touch II blood glucose monitoring system (Lifescan, Milpitas, CA, USA).
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7

Plasma Biomarker Profiling in Samples

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Blood samples (1 mL) were withdrawn by cardiac puncture and centrifuged at 12,000 g for 5 min at 4 °C. The supernatants of the blood samples were collected and subjected to the following measurements. Plasma levels of E2 were determined by luminescence immunoassay (Automated Chemiluminescence System, Bayer, Co. NY, USA); Plasma levels of adiponectin were measured using enzyme-linked immunosorbent assay kit (Abcam, Cambridge, MA, USA); Plasma glucose levels were detected by a One Touch II blood glucose monitoring system (Lifescan, Milpitas, CA, USA).
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8

Plasma Biomarkers in Sepsis Model

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Blood (1 mL) was taken at baseline and 24 hours after CLP from the carotid artery and centrifuged immediately (3 minutes, 16 000 × g) for measurement of plasma levels of alanine aminotransferase (ALT), blood urea nitrogen (BUN), creatinine, and lactate dehydrogenase (LDH). Plasma measurements were performed on a Fuji DRICHEM 3030 (Fuji Photo Film Co., Ltd., Tokyo, Japan). Each volume of blood withdrawn was replaced immediately by an equal volume of saline. Additionally, 10 μL of each blood sample was analyzed for blood glucose at baseline and 3 and 24 hours after CLP by using a One-Touch II blood glucose monitoring system (Lifescan Inc., Milpitas, CA, USA).
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9

Blood Glucose and Metabolic Panel

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We analysed the blood glucose levels in the samples (10 μl) using the OneTouch II blood glucose monitoring system (Lifescan, Milpitas, CA, USA). After immediate centrifugation at 16,000 g for 3 min, some samples were analysed for plasma levels of LDH, ALT, BUN, and creatinine using a Fuji DRICHEM 3030 (Fuji Photo Film, Tokyo, Japan). Each volume of blood withdrawn was replaced with an equal volume of saline.
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