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Milli q integral 10 system

Manufactured by Merck Group
Sourced in United States, Germany

The Milli-Q® INTEGRAL 10 system is a water purification system designed to produce ultra-pure water. It utilizes a combination of filtration and deionization technologies to remove contaminants and impurities from the water, producing water that meets the stringent specifications required for various laboratory applications.

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8 protocols using milli q integral 10 system

1

Trace Element Analysis Protocol

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The water used was 18 megohm water, purified with a Milli-Q® Integral 10 system (Merck, Darmstadt, Germany).
A selenium standard solution of 1000 mg/L, and a multi-element standard solution IV (at the concentration of 1000 mg/L): Ag, Al, Ba, Bi, Ca, Cd, Co, Cr, Cu, Fe, Ga, In, K, Mg, Mn, Na, Ni, Pb, Sr, Tl, Zn, were purchased from Merck KGaA (Darmstadt, Germany).
Calibration blank (Cal Blk) and calibration standard (Cal Std) solutions were prepared at concentrations of 0 μg/L (Cal Blk), 4 μg/L (Cal Std 1), 12 μg/L (Cal Std 2), and 20 μg/L (Cal Std 3), using the selenium standard stock solution, or multi-element standard stock solution, into separate 50 mL DigiTUBE® tubes (SCP SCIENCE, Baie-D’Urfe, QC, Canada) with the addition of 0.5 mL internal standard stock solution, 0.5 mL methanol and 5 mL concentrated nitric acid, and then diluted to the final volume with water.
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2

Trace Element Analysis in Pharmaceutical Sample

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Deionized water produced by a Milli-Q Integral 10 system (Merck, Germany) was used to prepare all solutions. Optima grade concentrated nitric acid (Fisher scientific chemical, USA) and analytical reagent 30% (m/m) hydrogen peroxide (Xilong Scientific, China) were employed in the sample preparation. ICP Multi-Element standard (5 elements, Bi, In, Sc, Tb, and Y at 100 mg/L in 2% (v/v) HNO3) was purchased from Reagecon (Ireland). ICP standard cadmium 1000 mg/L, ICP standard Lead 1000 mg/L, ICP standard arsenic 1000 mg/L, ICP standard cobalt 1000 mg/L, ICP standard vanadium 1000 mg/L, ICP standard nickel 1000 mg/L, ICP standard copper 1000 mg/L, and ICP standard lithium 1000 mg/L were purchased from Reagecon (Ireland). ICP standard mercury 1000 mg/L, ICP standard antimony 1000 mg/L, and ICP standard gold 1000 mg/L were obtained from National Non-ferrous Metals and Electronic Materials Analysis Center (China). Argon (99.999%) and helium (99.999%) gases were provided by Jinan Deyang Special Gas Co., LTD. (Shangdong, China). Parecoxib sodium was obtained from New Time Pharmaceutical Co. Ltd, Shang Dong, China.
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3

Glucose Metabolism Pathway Assay

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[U-13 C]-D-Glucose was purchased from SHOKO SCIENCE CO., LTD. (Kanagawa, Japan). TMG-123, a GKA, was synthesized in Teijin Pharma Limited (Tokyo, Japan). 7 All other reagents were analytical grade. Ultrapure water purified by a Milli-Q Integral 10 system (Merck Millipore, MA) was used throughout the study.
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4

Trace Element Analysis in Milk Samples

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All reagents were of analytical grade. Ultra-pure water (resistivity > 18.2 MΩ cm) was obtained from a Milli-Q® INTEGRAL 10 system (Millipore, MA, United States). Nitric acid (Vetec, Rio de Janeiro, Brazil) was purified by sub-boiling followed by distillation in a quartz still (Kürner Analysentechnik, Rosenheim, Germany). The multi-element standard solution Merck IV (Merck, São Paulo, Brazil), comprising 29 elements in diluted Nitric acid, was employed to prepare standard analytical curves. Two reference materials, certified Skimmed Milk Powder ERM®-BD150 (European Commission, Belgium) and Milk Powder 1549 (NIST SRM, United States) were used to assess method accuracy.
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5

Ultrapure Water and Nitric Acid Prep

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All reagents were of analytical grade. Ultra-pure water (resistivity > 18.2 MΩ cm) was obtained from a Milli-Q® INTEGRAL 10 system (Millipore Co., Billerica, MA, USA). Nitric acid (Vetec, RJ, BRA) was purified by sub-boiling followed by distillation in a quartz still (Kürner Analysentechnik, ROS, DEU). A multi-element standard solution Merck IV (Merck, SP, BRA), comprising 29 elements diluted in Nitric acid, was employed to construct the calibration curves.
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6

Trace Element Analysis of Milk Powder

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Standard solutions and reagents were purchased from Sigma-Aldrich Chemical Co. (St. Louis, MO, USA). All solvents, including methanol (MeOH), ethanol and acetonitrile with HPLC grade were purchased from Tedia Company Inc. (Rio de Janeiro, RJ, BRA). Agar yeast, extract glucose, chloramphenicol (YGC) and agar glucose and yeast extract were purchased from Hexis Científica (São Paulo, SP, BRA). Agar Man, Rogosa and Sharpe (MRS) was purchased from Acumedia (Lansing, MI, USA); 3M PetrifilmTM Salmonella Express Sy and 3M PetrifilmTM E. coli Count Plate were purchased from 3M Health Care (São Paulo, SP, BRA). All reagents were analytical grade. Nitric acid (Vetec, Rio de Janeiro, RJ, BRA) was purified by sub-boiling followed by distillation in a quartz still (Kürner Analysentechnik, Rosenheim, BY, DEU). The multi-element standard solution Merck IV (Merck, São Paulo, SP, BRA) comprising 29 elements in Nitric acid was employed to prepare standard analytical curves. Two reference materials, certified Skimmed Milk Powder ERM®-BD150 and Milk Powder 1549 were used to assess method accuracy (St. Louis, MO, USA). Ultra-pure water (resistivity > 18.2 MΩ cm) obtained from a Milli-Q® INTEGRAL 10 system (Millipore, Burlington MA, USA) was used to prepare all reagents.
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7

Extraction of Phenolic Compounds: Optimized Protocols

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The following compounds used for preparing extracts by targeted analysis of phenolic compounds and eluents were obtained commercially: resorcinol (Fluka, Germany), methanol (HPLC grade, VWR BDH Chemicals, Poole, United Kingdom), tetrahydrofuran (HPLC grade, VWR BDH Chemicals, Poole, United Kingdom), formic acid (Merck KGaA, Darmstadt, Germany), and orthophosphoric acid (85%, VWR BDH Chemicals, Poole, United Kingdom). Water used for extract and eluent preparation was purified by a Milli-Q Integral 10 system (Millipore, MA, United States).
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8

UPLC Mobile Phase Preparation

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HPLC grade acetonitrile (ACN, Sigma–Aldrich) was used in all UPLC mobile phases. All water used in these experiments was 18 MΩ water generated from an in-house system (Millipore Milli-Q Integral 10 system). UPLC vials were ‘Total Recovery’ 1 ml vials (Waters). 100 mM trieythl ammonium acetate (TEAA) was made by dilution of a commercial 2 M stock solution (Transgenomic). 100 mM tetraethyl ammonium bicarbonate (TEAB) was prepared by dilution of a 2 M TEAB stock. The 2 M TEAB was prepared by the drop wise addition of 278 ml of triethylamine to 700 ml of water while simultaneously bubbling carbon dioxide through the solution. The stock 2 M TEAB solution is stored at 4°C.
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