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3 μm c18 reverse phase hplc column

Manufactured by Dr. Maisch
Sourced in Germany

The 3 μm C18 reverse phase HPLC column is a laboratory equipment designed for high-performance liquid chromatography (HPLC) analysis. It features a stationary phase with a particle size of 3 micrometers and a C18 functional group, which is commonly used for the separation and analysis of a wide range of organic compounds.

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2 protocols using 3 μm c18 reverse phase hplc column

1

Quantifying Kynurenine and KYNA in Fetal and Maternal Tissues

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The tissue was weighed while frozen. After thawing, fetal brain (1:10, w/v) and placenta (1:10, w/v) were homogenized by sonication in ultrapure water (placental homogenate was further diluted 1:10, v/v, for KYNA determination). Maternal (1:4, v/v for kynurenine, 1:10, v/v for KYNA) and fetal (1:5, v/v for kynurenine, 1:20 v/v for KYNA) plasma were diluted in ultrapure water. Twenty-five μL of 25% perchloric acid were added to 100 μL of the tissue preparation, and precipitated proteins were removed by centrifugation (16,000 × g, 15 min). For determination ex vivo, the eluate was diluted 1:2 (v/v) in 6% perchloric acid and centrifuged (16,000 × g, 5 min).
For kynurenine and KYNA determination, 20 μL of each resulting supernatant were injected onto a 3 μm C18 reverse phase HPLC column (150 mm × 4 mm; Dr. Maisch GmbH, Ammerbuch, Germany), using a mobile phase containing 50 mM sodium acetate and 3% acetonitrile (pH adjusted to 6.2 with glacial acetic acid) at a flow rate of 0.5 mL/min. Zinc acetate (0.5 M; not pH adjusted), was delivered post column by a peristaltic pump (Dionex AXP, Thermo Fisher, Waltham, MA, USA) at a flow rate of 0.1 mL/min. In the eluate, analytes were detected fluorimetrically (kynurenine: excitation: 365 nm, emission: 480 nm; KYNA: excitation: 344 nm, emission: 398 nm; S200a fluorescence detector; Perkin Elmer, Waltham, MA, USA).
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2

HPLC Determination of KYNA

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For KYNA determination, 20 μL of the supernatant were applied to a 3 μm C18 reverse phase HPLC column (100 mm × 4 mm; Dr. Maisch GmbH, Ammerbuch, Germany), using a mobile phase containing 50 mM sodium acetate and 3% acetonitrile (pH adjusted to 6.2 with glacial acetic acid) at a flow rate of 0.5 ml/min. Zinc acetate (0.5 M, not pH adjusted) was delivered post-column by a peristaltic pump (Dionex AXP, Thermo Fisher, Waltham, MA, USA) at a flow rate of 0.1 ml/min. In the eluate, KYNA was detected fluorimetrically (excitation: 344 nm, emission: 398 nm; S200a fluorescence detector; Perkin Elmer, Waltham, MA, USA). The retention time of KYNA was approximately 14 min.
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