High-performance liquid chromatographic analysis of new triazole antifungal agent SYN-2869 and its derivatives in plasma

A simple reversed-phase high-performance liquid chromatography (HPLC) method with UV detection was developed and validated for the quantitation of SYN-2869, a novel triazole antifungal agent and its analogs in rat plasma. The method involved a simple precipitation of plasma protein with acetonitrile...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 1999-09, Vol.20 (5), p.791-797
Hauptverfasser: Khan, Jehangir K, Montaseri, Hashem, Poglod, Marzena, Bu, Hai-Zhi, Daneshtalab, Mohsen, Micetich, Ronald G
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container_end_page 797
container_issue 5
container_start_page 791
container_title Journal of pharmaceutical and biomedical analysis
container_volume 20
creator Khan, Jehangir K
Montaseri, Hashem
Poglod, Marzena
Bu, Hai-Zhi
Daneshtalab, Mohsen
Micetich, Ronald G
description A simple reversed-phase high-performance liquid chromatography (HPLC) method with UV detection was developed and validated for the quantitation of SYN-2869, a novel triazole antifungal agent and its analogs in rat plasma. The method involved a simple precipitation of plasma protein with acetonitrile (1:10 ratio). The reconstituted sample after evaporation to dryness was injected onto a HPLC column. SYN-2869 and its analogs were separated from the matrix components on a symmetry C18 column using an aqueous mobile phase of acetonitrile and water with a flow rate of 1 ml min −1. A step gradient of 40–80% acetonitrile eluted all four compounds. The run time was 30 min. The linear range was 0.5–10 μg ml −1 ( r 2>0.999). The limit of quantitation was 0.5 μg ml −1. The inter-day precision and accuracy for SYN-2869 standard concentration were from 1.9 to 8.5% and from −1.4 to +4.4%, respectively. The precision and accuracy of intra-day quality control samples were from 4.6 to 5.2% and from 4.6 to 12%, respectively.
doi_str_mv 10.1016/S0731-7085(99)00080-1
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The method involved a simple precipitation of plasma protein with acetonitrile (1:10 ratio). The reconstituted sample after evaporation to dryness was injected onto a HPLC column. SYN-2869 and its analogs were separated from the matrix components on a symmetry C18 column using an aqueous mobile phase of acetonitrile and water with a flow rate of 1 ml min −1. A step gradient of 40–80% acetonitrile eluted all four compounds. The run time was 30 min. The linear range was 0.5–10 μg ml −1 ( r 2&gt;0.999). The limit of quantitation was 0.5 μg ml −1. The inter-day precision and accuracy for SYN-2869 standard concentration were from 1.9 to 8.5% and from −1.4 to +4.4%, respectively. The precision and accuracy of intra-day quality control samples were from 4.6 to 5.2% and from 4.6 to 12%, respectively.</description><subject>Analysis</subject><subject>Animals</subject><subject>Antibiotics. Antiinfectious agents. 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subjects Analysis
Animals
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antifungal agents
Antifungal Agents - analysis
Antifungal Agents - blood
Antifungals
Azoles
Biological and medical sciences
Chromatography, High Pressure Liquid
General pharmacology
Medical sciences
Mice
Molecular Structure
Pharmacology. Drug treatments
Piperazines - analysis
Piperazines - blood
Piperazines - pharmacokinetics
Rats
Reproducibility of Results
Triazoles - analysis
Triazoles - blood
Triazoles - pharmacokinetics
title High-performance liquid chromatographic analysis of new triazole antifungal agent SYN-2869 and its derivatives in plasma
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