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Blood glucose analyzer

Manufactured by Roche
Sourced in Germany

The Blood Glucose Analyzer is a laboratory instrument designed to measure the concentration of glucose in blood samples. It provides accurate and reliable results to support clinical diagnosis and monitoring of glucose levels.

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Lab products found in correlation

3 protocols using blood glucose analyzer

1

Anti-inflammatory Effects of DM-sol and DM-gel in Diabetic Mice

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Diabetes causes changes in salivary secretion and composition, usually leading to dry mouth and/or hyposalivation.16 (link)–18 (link) Therefore, the anti-inflammatory effects of DM-sol and DM-gel were assessed in streptozotocin-induced diabetic mice after removal of submandibular glands, the major salivary glands in the mouth. Thirty-two female BALB/c mice were assigned to four groups (n=7–8 per group) to balance body weights (22–24 g). Mice were anesthetized by intraperitoneal injection of urethane (1.5 mg/kg), and then the submandibular gland, located beneath the lower jaws, was surgically removed using biopsy forceps. One week after excision of the submandibular gland, mice were intra-peritoneally administered 60 mg/kg streptozotocin (0.1 M citrate buffer, pH 4.5). Induction of diabetes was confirmed by monitoring the blood glucose level 72 h after injection of streptozotocin, using a blood glucose analyzer (Roche-Diagnostics 1, Mannheim, Germany). Mice with glucose levels >300 mg/100 mL were regarded as diabetic. About 20 μL of DM-sol, DM-gel, and normal saline as negative control were applied to the inner surface of the cheek using a micropipette four times per day for 4 weeks. The sham group received only normal saline and underwent neither removal of the submandibular gland nor injection of streptozotocin during the same period.
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2

Comprehensive Serum and Fecal Analysis

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Total serum cholesterol (TC) and low density lipoprotein cholesterol (LDL-C) were measured using an automatic biochemical analyzer. FBG, serum insulin (INS), and serum ROS were measured using a Roche blood glucose analyzer, a radioimmunoassay, and an ELISA kit, respectively. Rat fecal sample DNA purity and concentration were determined using a NanoDrop2000 ultramicrospectrophotometer. DNA integrity was determined using agarose gel electrophoresis and microecological detection was performed when DNA purity was established.
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3

Establishment of Diabetic Neuropathic Pain Model

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Male SD rats (provided by animal experiment center, Hebei Medical University) aged 3 weeks old and weighing 150–170 g were used in this study. The rats were kept at 20–25°C with a normal light-dark cycle and free access to food and water after 3 days of adaptation. A total of 100 rats were randomly assigned to induce DNP as reported previously [4 (link)]. Briefly, the rats were fasted for 12 hours followed by peritoneal injection (i.p.) of STZ (60 mg/kg, Sigma) freshly dissolved in 0.1 mol/l citric acid buffer (pH 4.5) or were used as nondiabetic controls. After 7 days, blood samples were extracted from the tail vein of rats and blood glucose levels were measured using a blood glucose analyzer (Roche, Germany). Blood glucose level ≥ 16.7 mmol/l was considered hyperglycemic and deemed successful for establishment of diabetes. The paw withdrawal threshold (PWT) was measured 2 weeks after STZ injection according to the protocol of Dixon [19 (link)]. Blood glucose level > 16.7 mmol/l and PWT < 6 g were used as the cut-off criteria for successful model of DNP. DNP was successfully induced in 72 rats. Twelve rats were injected i.p. with equal volume of saline as normal controls.
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