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Arium pro purification system

Manufactured by Sartorius

The Arium Pro water purification system is designed to produce ultrapure water for laboratory applications. It utilizes a multi-stage filtration process to remove contaminants and deliver consistently high-quality water for critical experiments and analyses.

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3 protocols using arium pro purification system

1

Extraction and Analysis of Toxins by LC-MS

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LC-MS grade methanol (MeOH) and acetonitrile (CH3CN) were used for the extraction and analyses of toxins by liquid chromatography coupled to mass spectrometry (LC-MS). Analytical-grade ammonium hydroxide, sodium hydroxide (NaOH), and hydrochloric acid (HCl) were used for the mobile phase and hydrolysis. Ultrapure water was obtained with a Sartorius (Arium Pro) purification system. Certified reference solutions for okadaic acid CRM-OA-d (batch #20141119), dinophysistoxin-2 CRM-DTX2-b (batch #20150819), dinophysistoxin-1 CRM-DTX1-b (batch #20151209), and pectenotoxin-2 CRM-PTX2-b (batch #20120516) were obtained from NRC-CNRC.
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2

Canagliflozin Formulation: Improving Solubility

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Canagliflozin (hemihydrate, D90: 18.119 µm) was purchased from Fuxin Long Rui Pharmaceutical CO., Ltd. (Fuxin, China). Hydroxyl propyl methyl cellulose 15 cP (Methocel®E15 LV) was obtained from Colorcon Middle East Pvt. Lt. (Istanbul, Turkey). Soluplus®, poloxamer 188 (P188, Kolliphor® P188), poloxamer 407 (P407, Kolliphor® P407), sodium lauryl sulfate (SLS, Kolliphor® SLS fine), polyvinylpyrrolidone—polyvinyl acetate copolymers (PVP VA64, Kollidon® VA 64) and polyvinylpyrrolidone (PVP K30, Kollidon® 30) were obtained from BASF, Ludwigshafen, Germany. Polysorbate 80 (Tween® 80) and polysorbate 20 (Tween® 20) were taken from Sigma-Aldrich Chemie GmbH, Steinheim, Germany. Methanol, acetonitrile (HPLC grade) and 85% ortho-phosphoric acid were obtained from MERCK Millipore, Darmstadt, Germany and ISOLAB, Wertheim, Germany, respectively. Ultrapure water was prepared by using a Sartorius Arium Pro purification system.
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3

Biophysical Characterization of Nucleic Acids

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The aqueous buffer used was NaCl 0.1 M, NaCac 2.5 mM (Cac = cacodylate) pH = 7.0, with the exception of the melting experiment with CT-DNA where the buffer was NaCac 2.5 mM pH = 7.0. For the experiments with G4s the buffer was KCl 0.1M LiCac 2.5mM pH 7.0 for the titrations and melting analysis, while for the mass spectrometry the buffer was NH 4 OAc 0.1M pH 7.0. Ultra-pure water from an ultra-pure Sartorius Arium-pro purification system was used throughout. Common reagents were the commercial analytical grade compounds and were used as received.
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