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1290 lc system

Manufactured by Waters Corporation

The 1290 LC system is a high-performance liquid chromatography (HPLC) instrument manufactured by Waters Corporation. It is designed to provide efficient and reliable liquid chromatography separation and analysis. The 1290 LC system features advanced technology and components to deliver accurate and reproducible results.

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2 protocols using 1290 lc system

1

Quantitative Bile Acid Profiling in CSF

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The target
study of BAs used an Agilent 1290 LC system (Waters C18 column, 1.7
μm, 2.1 × 150 mm) coupled with a Sciex 7500 QQQ MS in a
multiple-reaction monitoring (MRM) mode with (−) detection,
as described by Han et al.45 (link) A 10 μM
standard mixture (94 BAs in total, Table S7) was prepared in an IS solution of UDCA-D4 in MeCN. Next,
60 μL of each CSF sample was mixed with 140 μL of the
IS solution, vortexed, sonicated, centrifuged, then dried, and dissolved
in 40 μL of 50% MeCN. Fifteen microliters per sample was injected
in the LC–MS system. BA concentrations were calculated by interpolating
the constructed IS calibrated linear–regression curves of individual
BAs, with the peak area ratios measured from injections of the sample
solutions.
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2

Investigating Fenofibrate Release from MMC

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A shift in the UV spectrum occurred during the release of fenofibrate-loaded MMC, so UPLC-MS was used to determine the origin of the shift. Two samples were weighed into Eppendorf tubes, one with 8 mg fenofibrate-loaded MMC and the other with 0.7 mg crystalline fenofibrate and 7.2 mg MMC. Two milliliters of Milli-Q water was added to the tubes, which were then placed on a plate shaker at 37 °C for 24 h. The supernatants were recovered by centrifugation at 37 °C for 15 min at 23,000×g (Heraeus Megafuge 8R, ThermoScientific) and analyzed by obtaining a full MS spectrum (QTRAP 6500, AB Sciex). A stock solution of fenofibrate dissolved in DMSO was used as reference. Separation was performed on an Agilent 1290 LC-system, with a Waters BEH C18 2.1 × 50 mm (1.7 μm) column, and the run was made in positive mode. The mobile phase consisted of (A) 5% acetonitrile, 0.1% formic acid, and 94.9% Milli-Q water; and (B) 95% acetonitrile, 0.1% formic acid, and 4.9% Milli-Q water. A constant flow rate of 0.5 mL/ min was used for the gradient elution as follows: A was constant at 99% for 1.0 min, then decreased linearly to 20% for 7.30 min. A was thereafter decreased to 10% for 0.2 min, kept constant for 0.5 min, and then increased to 99% for 0.5 min.
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