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Lc ac system

Manufactured by AB Sciex

The LC AC system is a high-performance liquid chromatography (HPLC) instrument designed for analytical and preparative applications. It provides precise control and monitoring of the liquid chromatography process, ensuring consistent and reliable separations. The core function of the LC AC system is to deliver mobile phases, introduce samples, and separate analytes based on their physical and chemical properties.

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4 protocols using lc ac system

1

Polyphenol Quantification by LC-MS/MS

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The sample was analyzed with liquid chromatography−electrospray ionization−tandem mass spectrometry (LC–ESI–MS/MS) using an Exion LC AC system for separation and a SCIEX Triple Quad 5500 + MS/MS system with ESI for detection. For the separation, a ZORBAX Eclipse Plus C18 Column (4.6100 mm, 1.8 m) was used. The mobile phase was 0.1% formic acid in water (solvent A) and acetonitrile (solvent B) with the following gradient: 2% B from 0–1 min, 2–60% B from 1–8 min, 60% B from 8–12 min, and 2% B from 12.01–15 min. The flow rate was 0.8 mL/min and the injection volume was 3 µL. The selected polyphenols were analyzed using the negative ionization mode using Multiple Reaction Monitoring (MRM). The curtain gas was 25 psi, the ion spray voltage was 4500, the source temperature was 400 °C, the ion source gases 1 and 2 were 55 psi with a declustering potential of 50, the collision energy was 25 eV and the collision energy spread was 10 eV.
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2

LC-ESI-MS/MS Analysis of L. rhamnosus Polyphenols

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The L. rhamnosus ethyl acetate extract No. 5 was analysed with liquid chromatography-electrospray ionization–tandem mass spectrometry (LC-ESI-MS/MS). Exion LC AC system for separation and a SCIEX Triple Quad 5500+ MS/MS system with electrospray ionization (ESI) was used for the detection. ZORBAX SB-C18 Column (4.6 × 100 mm, 1.8 µm) (Agilent Technologies, USA) was used for the separation. The mobile phases comprised two eluents: A (0.1% formic acid in water) and B (acetonitrile). The mobile phase was programmed as follows: 2% B from 0 to 1 min., 2% B from 1 to 21 min., 60% B from 21 to 25 min., and 2% B from 25 to 28 min. The injection volume was 3 µL, and the flow rate was 0.8 mL/min. Positive and negative ionization modes were used in the same run for MRM analysis of the selected polyphenols, using the following parameters: Ion spray voltage: 4500 and - 4500 for positive and negative modes, respectively; curtain gas: 25 kPa; source temperature: 400 °C; ion source gases 1 and 2 were 55 kPa with a de-clustering potential of 50; collision energy: 25; collision energy spread: 10.
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3

Comprehensive Analysis of Propolis Extracts

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The analysis of crude propolis, nano-capsules propolis extracts by slovent and SCF-CO2 at 50 °C was performed using liquid chromatography–electro-spray ionization–tandem mass spectrometry (LC–ESI–MS/MS) with an Exion LC/AC system for separation and SCIEX Triple Quad 5500+ MS/MS system equipped with an electro-spray ionization (ESI) for detection. The instrument data were collected and processed using the SCIEX OS 1.6.10.40973 software.
The separation of the targeted analyses was performed with a Discovery® BIO Wide Pore C18-5 Column (4.6 × 250 mm, 5 µm). The mobile phases were consisted of two eluents A: 0.1% formic acid in water; B: 0.1% formic acid in acetonitrile (LC grade). The mobile phase gradient was programmed as follows: 5% B at 0 min, 5–25% B from 0.0 to 60.0 min, 25–5% B from 60 to 65 min, 5% from 65 to 70. The flow rate was 1.0 ml/min and the injection volume was 5 µl. For MS/MS analysis, negative ionization mode was applied with a scan (EMS-IDA-EPI) from 150 to 800 Da with the following parameters: curtain gas: 25 psi; ion spray voltage: −4500; source temperature: 400 °C; ion source gas 1 & 2 were 55 psi.
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4

Polyphenol Analysis by LC-MS/MS

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Liquid chromatography-electrospray ionization–tandem mass spectrometry (LC-ESI-MS/MS) of the samples used an Exion LC AC system for separation and SCIEX Triple Quad 5500+ MS/MS system equipped with electrospray ionization (ESI) for detection. The separation was performed using ZORBAX SB-C18 Column (4.6 × 100 mm, 1.8 µm). The mobile phases were mainly from two eluents, A: 0.1% formic acid in water and B: acetonitrile (L.C. grade). The mobile phase was programmed as follows: 2% B from 0–1 min, 2–60% B from 1–21 min, 60% B from 21–25 min, and 2% B from 25.01–28 min. The flow rate was 0.8 mL/min, and the injected volume was 3 µL. For multiple reaction monitoring (MRM) analysis of the selected polyphenols, positive and negative ionization modes were applied in the same run with the following parameters: curtain gas: 25 psi; ion spray voltage: 4500 and 4500 V for positive and negative modes, respectively; source temperature: 400 °C; ion source gas 1 and 2 were 55 psi with a declustering potential (DP): 50; collision energy: 25 eV; collision energy spread: 10 times [11 (link)].
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