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Model 1260 hip als autosampler

Manufactured by Agilent Technologies

The Model 1260 Hip ALS autosampler is a laboratory equipment product offered by Agilent Technologies. It is designed to automatically introduce samples into an analytical instrument for analysis. The core function of this product is to provide automated sample handling and injection capabilities to support various analytical techniques.

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2 protocols using model 1260 hip als autosampler

1

HPLC Analysis of Praziquantel

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High-Performance Liquid Chromatography Agilent 1260 Infinity II HPLC system (Agilent Technologies, Inc.) equipped with Model 1260 quaternary pump, Model 1260 Hip ALS autosampler, Model 1290 thermostat, Model 1260 TCC control module, and Model 1260 diode array detector was utilized as described previously. Data processing and analysis was performed using OpenLab CDS software (Agilent Technologies, Inc.). For praziquantel, chromatographic isocratic separation was carried out on an Agilent Zorbax Eclipse XDB C-18 4.6 × 150 mm analytical column with 5 μm particles, maintained at 40 °C. The optimized mobile phase consisted of MilliQ grade water and acetonitrile at a flow rate of 1 ml/min over a 5 minutes run time. Separation was achieved using a gradient elution profile starting at 50% water and 50% acetonitrile at minute 0 which ended at 30% water and 70% acetonitrile at 3 minutes. The injection volume was 5 μl, and the selected ultraviolet (UV) detection wavelength was 217 nm.
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2

HPLC Analysis of Drug Concentration

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Drug concentration was analyzed using Agilent 1260 Infinity HPLC system equipped with Model 1260 quaternary pump, Model 1260 Hip ALS autosampler, Model 1290 thermostat, Model 1260 TCC control module, and Model 1260 diode array detector. The output signal was monitored and processed using Agilent ChemStation software. Chromatographic separation was carried out on a 50-mm × 4.6-mm EC-C18 Agilent Poroshell 120 analytical column with 2.7-µm spherical particles, maintained at 40 °C.
For samples in MeOH: DMSO solution, the optimized mobile phase consisted of a gradient elution of methanol: water (pH 3.5 adjusted with 0.1% formic acid) (0 minute (min), 30:70 v/v; 4 min, 30:70; 4.5 min, 90:10; 7 min, 90:10; 7.5 min, 30:70) at flow rate of 1.1 mL/min over a 12-min run time. The injection volume was 20 µL, and the UV detection wavelength of 360 nm was selected.
For samples in simulated gastric fluid (SGF, which consists of 0.2% w/v sodium chloride, 0.7% w/v hydrochloric acid, deionized water, pH 1.2), the optimized mobile phase consisted of a gradient elution of methanol: water (pH 3.5 adjusted with 0.1% formic acid) (0 min, 30:70 v/v; 3.5 min, 70:30; 6.5 min, 70:30; 7.5 min, 30:70) at flow rate of 1.0 mL/min over a 10-min run time. The injection volume was 50 µL, and the UV detection wavelength of 360 nm was selected.
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