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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Determination of ASP3258, a novel phosphodiesterase type 4 inhibitor, in rat plasma by high-performance liquid chromatography with fluorescence detection and its application to pharmacokinetic study
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Determination of ASP3258, a novel phosphodiesterase type 4 inhibitor, in rat plasma by high-performance liquid chromatography with fluorescence detection and its application to pharmacokinetic study

机译:高效液相色谱-荧光检测法测定大鼠血浆中新型4型磷酸二酯酶抑制剂ASP3258的含量及其在药代动力学研究中的应用

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摘要

The potent phosphodiesterase 4 inhibitor ASP3258 contains a carboxylic acid moiety and a naphthyridine ring and is a novel therapeutic agent for asthma and chronic obstructive pulmonary disease. To support the drug development of ASP3258, we developed and validated a simple method for its determination in rat plasma. Following the addition of the analog AS1406604-00 as an internal standard, plasma samples were processed using C-18-bonded solid-phase extraction cartridges under acidic conditions and injected into a high-performance liquid chromatography system with fluorescence detection. Chromatographic separation was achieved on a Shiseido Capcell Pak C-18 UG120 column (3.0x150mm, 5 mu m) with a mobile phase consisting of acetonitrile-0.5% acetic acid (50:50, v/v). HPLC eluent was monitored with a fluorescence detector set at a wavelength of 315nm for excitation and 365nm for emission. The calibration curve was linear over a range of 2.5-250ng/mL. Validation data demonstrated that the method is selective, sensitive and accurate. In addition, the present method was successfully applied to rat plasma samples from a pharmacokinetic study. Copyright (c) 2014 John Wiley & Sons, Ltd.
机译:有效的磷酸二酯酶4抑制剂ASP3258含有一个羧酸部分和一个萘啶环,是一种用于哮喘和慢性阻塞性肺疾病的新型治疗剂。为了支持ASP3258的药物开发,我们开发并验证了在大鼠血浆中测定其的简单方法。在添加类似物AS1406604-00作为内标之后,使用C-18键合固相萃取柱在酸性条件下处理血浆样品,并将其注入具有荧光检测功能的高效液相色谱系统中。在Shiseido Capcell Pak C-18 UG120色谱柱(3.0x150mm,5μm)上进行色谱分离,流动相由乙腈-0.5%乙酸(50:50,v / v)组成。用荧光检测器监测HPLC洗脱液,荧光检测器设置为激发波长为315nm,发射波长为365nm。校准曲线在2.5-250ng / mL范围内呈线性。验证数据表明该方法具有选择性,灵敏性和准确性。另外,本方法成功地应用于来自药代动力学研究的大鼠血浆样品。版权所有(c)2014 John Wiley&Sons,Ltd.

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